tag:blogger.com,1999:blog-92077425913077909872024-03-07T23:41:36.144-08:00LYME,THE ROLLERCOASTER!Lyme Disease
my experience!MJhttp://www.blogger.com/profile/16614021020877246061noreply@blogger.comBlogger35125tag:blogger.com,1999:blog-9207742591307790987.post-33958622519647607012013-02-27T18:15:00.000-08:002013-02-27T22:20:02.227-08:00LYME ANTHELMINTICS DOSING!<span style="font-size: x-large;">My FB friend T asked me: </span><br />
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<span style="font-size: x-large;"><span style="font-family: "Times New Roman","serif";">"Hi Maria, What do you feel is the best Ivermectin dose? I too believe that a parasitic
infection makes the most amount of sense, especially after rounds of Albendazole etc. have made me feel symptom free at certain stages of the
illness. Love your work, T.</span></span></div>
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<span style="font-size: x-large;">Hello T,</span></div>
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<span style="font-size: x-large;"><span style="font-family: "Times New Roman","serif";">T</span>he more I research I
do, and the more logic to use, is that Lyme is a multiinfection bacterial
yes, but for sure parasitic if not by name by action of the bugs. Borrelia goes inside the cells, Mycoplasma
too, and all the coinfections like Bartonella and Erlichia too? Obviously Babesia is a parasite inside the
blood so it has to be added to the pot of Lyme, and then the studies of Dr Sapi in the UNH, the Boronson's in Norway and Dr
Fry in Texas, all talking about
protozoans and parasites cannot be ignored as if it not happening? .. its even
funny to hear it is a bacterial infection when it really is the least bacterial
..? I think if this concept is changed treatment could be more accurate... Why? just because you
don't kill parasites with antibiotics, as you don't kill snakes with flea
spray!!</span></div>
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<span style="font-size: x-large;">The dose of
Ivermectin that my Colombian Dr told me is one drop per one kilogram of weight,
in the human drops that come at 0.6% concentration, given once a week. This means the medicine is not administered
daily, as US Drs do with the Stromectol, because the Ivermectin and the
veterinary IVOMEC (1%) stay in the body 4 to 5 days until totally eliminated. I wonder why the Stromectol is given every
day? Second it means a dose given
according to the person, not a formula for everybody. In my "calculations" I get around 3
to max 12 mgs of medicine a week, while here the dose is 12 mgs three times a
day every day? ... its so high it doesn't makes sense to me...</span></div>
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<span style="font-size: x-large;">My Col Dr said; an acute infection should be treated with
higher doses but in a short period of time, let's say two weeks max 4
weeks. While a chronic long term
multiinfected patient should receive low doses for long time to clean the
infection and tons of detoxing!</span></div>
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<span style="font-size: x-large;">The
"Azoles" are the proper medicines for parasites in our case more than
antimalarics due to these last ones work by immune suppression and we don't
need that...:) The Albenda is the
"oldest" one and stronger. It
kills malaria too, but in long term treatment it can affect the Central Nervous
system. Studies in children found they
were having similar symptoms as Parkinson's such as involuntary movements, etc,
so it looks like Albenda is not for Lymies in the long run, maybe just for a
short two weeks support. The feared
Flagyl - Metronidazole- is the always good old treatment but here in the US Drs
give 2 grs a day or IV even stronger, it can blow the liver and the heart... my
Dr told me to not use more than 750 mgs a day!!! See? Dosing!</span></div>
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<span style="font-size: x-large;">And from the Azoles,
the Tinidazole, in the US known as Tindamax or "Tini" how we call it,
is the youngest of the family, and it has been studied lately thank God by or
dear Dr. Eva Sapi, who found protozoan component in Lyme Disease, and she found
Tini does more than Doxy in the Lyme treatment and if you decide to use the
Doxy better accompany it with Tini to get better results; this because Doxy
alone as per CDC recommendations would only push the bacteria to go cystic
faster and people get sicker faster too! In my personal case Tindamax was not a
medicine that I felt helped me as I can swear over flagyl and Ivermectin... I
thought it was too mild and blah.. maybe for all the Lymies who have not had
any kind of anthelmintics – antiparasitics- this could save their lives?
Because tindamax and these types of medicines kill the bacteria and also
ruptures the cysts! (I attached some links of interesting articles written by
Dr Sapi and Dr J about Tindamax, below). </span></div>
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<span style="font-size: x-large;"> So why Ivermectin? because studies show that it can even help
with parasites, some types of bacteria and even some fungal infections? And
because it has helped me so much!!! There is so much to it and US Drs don’t
even want to try it??? I swear over the
bible I have no commercial interest in this medicine and I talk about it
because it helps me and has helped so many I found on my path, so I share the
info so each one decide if to take it or not.
I wish I could educate Drs and researchers about it. I have given samples for free to patients,
Drs and researchers and the results are amazing… I hope it is included in most
protocols!</span></div>
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<span style="font-size: x-large;">Thank you for sharing
with me and saying you "love my work", I only share what I have
learned hoping it helps others, and I'm thankful with God for giving me this
opportunity!</span></div>
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<span style="font-size: x-large;">Hope I responded your
question. I cannot tell anyone how to
dose because I am not a Dr, so you made the right question indeed! </span></div>
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<span style="font-size: x-large;">God bless you, God is
big!</span></div>
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<span style="font-size: x-large;">Note: here is one
of the studies of Dr Sapi about the use
of Tindamax: </span></div>
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<span style="font-size: x-large;"><a href="http://www.dovepress.com/evaluation-of-in-vitro-antibiotic-susceptibility-of-different-morpholo-peer-reviewed-article-IDR">http://www.dovepress.com/evaluation-of-in-vitro-antibiotic-susceptibility-of-different-morpholo-peer-reviewed-article-IDR</a></span></div>
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<span style="font-size: x-large;">And this is a piece
of the blog of Dr J in his blog LYMEMD, his amazing findings about Tindamax and his input
about Dr Sapi’s studies: “I cannot
cover the whole Sapi study. The most exciting finding is that Tindamax
(Tinidazole) - our premier Cyst-buster, is the most effective drug overall.
This "cyst-buster" kills 90% of cysts and spirochetes: by far the
best drug. We don't know it's effect on L-forms, but we can guess. Tindamax
probably works by an intracellular mechanism. If this is true it should be
equally effective against L-forms. <span style="font-size: x-large;"></span>It gets even better. Tindamax is the only drug which does a great job on
biofilm colonies as well! (not to be discussed now). More on biofilms later. <br />
Tindamax passes the blood brain barrier and penetrates well into most tissues.
It has been effective in my patients with neurocognitive deficits -
neuroborreliosis.” The complete blog is here: <a href="http://lymemd.blogspot.com/2011/07/everything-you-thought-you-knew-about.html">http://lymemd.blogspot.com/2011/07/everything-you-thought-you-knew-about.html</a></span></div>
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<span style="font-size: large;">I just hope testing would be more reliable so people who is recently infected could be treated properly and soon enough so they won't suffer so long and so much as we had.!</span></div>
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<span style="font-size: large;">Maria.</span><br />
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<span style="font-size: large;"><b><span style="font-size: x-small;">NOTE: LYME THE ROLLERCOASTER BLOG DOES NOT OFFER, DOESN'T GIVES<span style="font-size: x-small;">, </span> NOR INTENDS TO GIVE ANY MEDICAL ADVISE NOR MEDICAL RECOMMENDATIONS.</span> </b></span></div>
MJhttp://www.blogger.com/profile/16614021020877246061noreply@blogger.com0tag:blogger.com,1999:blog-9207742591307790987.post-89631474076288165782013-02-25T15:15:00.003-08:002013-02-27T22:20:16.423-08:00LYME DISEASE, TRUST YOUR GUT!!<span style="font-size: x-large;">Some were wondering if I got cured from Lyme Disease, or if I was sicker, because I was not posting anything here. I can say I stopped writing this blog because I dedicated to my group called Florida Lyme League and was bringing all the research to them and to my wall in Facebook, so now I'm back and hopefully soon I will start a new blog with videos that I think are going to be very teaching helpful for all.</span><br />
<span style="font-size: x-large;">I have learned a lot about Lyme and Chronic diseases but I guess I have learned much more about human nature and also about my body and about what to do when I'm not feeling well.So I'm not writing this blog today about Lyme or the human nature but about what to do when you feel this sick and are so desperate and cannot find answers in the Doctors or the internet nor your closer people can help you? I say pray with what ever words you have and what ever faith you have, and ask for personal knowledge and then, with no doubt FOLLOW YOUR GUT! It doesn't fail! I'll give you some examples.</span><br />
<span style="font-size: x-large;">My friend was told to drink a lot of water, to detox, so she calls me and tells me that every time she drank a lot of water she got swollen and got terrible pains all over, I just asked her, so what do you think you should do? She said I cannot have all that water, it is not helping me... see? She had the answer to her problem. Then the point was to find the cause why she is retaining liquids and getting swollen? Maybe the gallbladder is blocked and the Lymphatic system is not running properly? Maybe the kidney is producing more water or not processing it properly? Maybe your adrenals are in fear mode, and they're telling the kidney to fill everything with water to "clean the mess"? Maybe it is a allergy with mold and the body is trying to wash it out..? I can go long with this reasoning and probably I still be missing the cause - which of course in a person with Lyme the base cause<b> </b>is probably a pathogenic - a "bugs cause"; but what I try to say here is that if we follow our guts we might know, first hand, what to do and then we can try to find the cause to fix the problem from the base.</span><br />
<span style="font-size: x-large;">More over, we could stop our selves from more symptoms for example, headaches. I start looking when I got them and then trying to find why? so I noticed that every time I eat dessert I got a terrible headache and worse I got so moody and I could even become very angry... so, no need to get a lab test to tell me I am having sugar problems, Nor i needed a Doctor to tell me I needed to make an effort and stop it from my diet. Same thing with the gluten. I don't have a Dr telling me I have to be in a "gluten free diet", I found it by stopping all gluten for two weeks and seeing that my body swelling started to come down... while my friends who have a Dr telling them to do the restriction they have gluten "every now and then" thinking the Dr won't notice it.. :) Same with sugars and even alcohol... My friend from the Group has chocolates and peanut butter almost every day regardless of her Doctor's recommendations. One day she showed me her back full of blisters filled of infection, I asked her if this could be her liver or a result of eating fats or chocolates? And she immediately responded very defensive that she was never going to quit the chocolate "because it is the only thing I have left"... I wonder if life and health is not the ultimate "thing" we should keep? </span><br />
<span style="background-color: #38761d; font-size: x-large;"><b>So this means that if you follow your gut and you really want to recover you are going to have to do changes with a strong personal will over what ever anyone tells you to do or not. It is like quitting a vice "cold turkey". It is a personal way and there is no other way to do it!</b></span><br />
<span style="font-size: x-large;">When following my gut I found my swelling comes from bacteria/parasitic infection, that clogged my blood, my gut, my gallbladder and liver and the glands of my body. With this I have to see what to do to help the body to recover. Diet is one, exercise could be other option but my body seems to not be able to take it yet, so I started with something "easier" like trying to be able to sweat! I had the neurological Lyme that affected the part of the brain that won't let me sweat nor recover the heat - sympathetic / parasympathetic functions were diminished - but after treatments with some oral antibiotics and Ivermectin - antiparasitics- and the very blessed "Double helix water" I found I started to sweat, a little - so I searched for a infrared sauna until found one suited to my small pocket and I think I have now recovered my ability to sweat and with this I started to detox and liberate my body from swelling and toxins.</span><br />
<span style="background-color: #bf9000; font-size: x-large;"><b>See? little remedies and small changes can make a huge impact in our health. But our body will always tell if the medicine, the treatment, the remedy or the change is good or not, and even before having any treatment our gut is telling us what is needed to help our selves. </b></span><br />
<span style="font-size: x-large;">With this I would like to make a side note about what we call "<b>HERXING</b>". We have learned that when we treat for Lyme Disease the body reaction is so strong we feel much sicker, sounds to be obvious after having so much infection spread all over; but I have learned some Lymies and even Doctors only guide their treatment to when they feel the sicker thinking they are having a huge herx, meaning a great response of their bodies., but I confess I've done quite the opposite... I learned from the Dr writer of the blog LYMEMD, from my Colombian Doctor and from Integrative Doctors such as Dr Lee Cowden, that suffering doesn't mean we are healing, it could be a misconception and guide us in a wrong way. Dr J states that if you don't start to feel any better after two weeks of treatment you better start thinking what to do next. Dr Cowden has a protocol, herbal, that includes Burbur and other medicines that will help to deal with the strongest herxings, without this being a cover up of what is going on with the disease. My Col Dr used the "old logic": if it doesn't help you feel better what for you treat"? and he taught me to always keep checking the reactions of my body, after every med taken, after every food, and every remedy. I found that when I took my once a week dose of Ivermectin, the antiparasitic so feared int he US but so used in South America and Africa, not only I had a mild herx the first two days but then I start having a couple of hours a day feeling a bit better. Some without Lyme won't understand what is to have a "couple of good hours" but for us who suffer this disease we know this is priceless. So after this I decided I will look more for "good herxing" than feeling sicker. I can take an antibiotic and can tell exactly when it is kicking in, what is it doing and after a couple of days I can tell if it is working to my recovery or not. Doesn't mean I change treatments every day, by the contrary, I stick with the ones that have really helped me and this has been what has kept me alive and living a decent life during all these years of nightmare.</span><br />
<span style="font-size: x-large;">Follow your gut is believing that your body is telling you what is the problem and what it needs. Help your self studying, reading, watching videos and doing all it takes to find answers and responses to your needs. Do not stay with thinking you are sick and one week of antibiotics is all you can have, it is a lie orchestrated to save money of the insurances that don't want to pay for longer treatment. Do not stay still without looking for other treatments out of the box, like a simple adding bicarbonate to your water or taking castor oil to detox your colon - or a colonic or a coffee enema -. You have the strength to recover, count on it!</span><br />
<span style="font-size: x-large;"><span style="font-size: x-large;">BLESSINGS!</span></span><br />
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<span style="font-size: large;"><b><span style="font-size: x-small;">NOTE: LYME THE ROLLERCOASTER BLOG DOES NOT OFFER, DOESN'T GIVES<span style="font-size: x-small;">, </span> NOR INTENDS TO GIVE ANY MEDICAL ADVISE NOR MEDICAL RECOMMENDATIONS.</span> </b></span>MJhttp://www.blogger.com/profile/16614021020877246061noreply@blogger.comtag:blogger.com,1999:blog-9207742591307790987.post-235669164843435882011-11-16T12:28:00.000-08:002013-02-27T22:20:28.542-08:00LYME DISEASE, DO NOT TAKE ANTIMALARIALS!<h6 class="uiStreamMessage" data-ft="{"type":1}">
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<span style="font-size: large;">Will start to share here the dialogs I have in my <span style="font-size: large;">F</span>acebook page with my Lymie friends. I have more than 800 friends with Lyme Disease in the US and the world; and 400 in Florida; yes Lyme Disease is real! Note: will not show the names of my friends<span style="font-size: large;"> </span>unless they give me permission to do it.</span></div>
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<span style="font-size: large;"><a data-hovercard="/ajax/hovercard/user.php?id=100000717846530" href="https://www.facebook.com/LYMEMJ">Maria LymeDisease</a></span></div>
<span style="font-size: large;"> <span class="messageBody" data-ft="{"type":3}">CONFIRMED: ALL ANIMALARIALS ARE IMMUNOSUPPRESSANTS not good for Lymies!!! Included Mepron or Atovaquone, Qinnine, Plaquenil, (Hydroxychloroquine), Clindamicin and other. Yes we need to treat Babesia, the parasite inside the blood <span style="font-size: large;">transmitted</span> by the tick, kind of similar to the malaria falsiparum parasite, but because we have another lot more of infections going on, transmitted by the tick at the same time that we call "co-infections" we should not, must not, take anything to suppress our Immune system; this is the reason why my Dr said to better take "anthelmintics"! <a href="http://en.wikipedia.org/wiki/Anthelmintic" rel="nofollow nofollow" target="_blank">http://en.wikipedia.org/wiki/A<wbr></wbr>nthelmintic</a></span></span></h6>
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<span style="font-size: large;"><b><a href="http://en.wikipedia.org/wiki/Anthelmintic" rel="nofollow" target="_blank">Anthelmintic - Wikipedia, the free encyclopedia</a></b></span> </div>
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<span style="font-size: large;">Anthelmintics or antihelminthics are drugs that expel parasitic worms (helminths) from the body, by either stunning or killing them. They may also be called vermifuges (stunning) or vermicides (killing)</span></div>
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<span style="font-size: large;"><span class="UIActionLinks UIActionLinks_bottom" data-ft="{"type":"20"}"></span><span class="uiStreamSource" data-ft="{"type":26}"></span>Note: the few Doctors in the US that dare to give anthelmintics for Lyme are treating with ALBENDAZOLE which was demonstrated to cause damage in the Central Nervous system, this was seen in children who were presenting symptoms like Parkinson's; Ivermectin was found to be the less damaging and the best anthelmintic ever created. No I don't sell anything, just sharing my research and experience.</span><br />
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<span style="font-size: large;"><abbr class="timestamp livetimestamp" data-date="Wed, 16 Nov 2011 10:57:27 -0800" title="Wednesday, November 16, 2011 at 1:57pm"></abbr><span class="comment_like_496204 fsm fwn fcg" data-ft="{"type":36}"></span><a class="actorPic UIImageBlock_Image UIImageBlock_SMALL_Image" data-ft="{"type":34}" data-hovercard="/ajax/hovercard/user.php?id=1116884388" href="https://www.facebook.com/profile.php?id=1116884388" tabindex="-1"><br />
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<span style="font-size: large;"><a class="actorName" data-ft="{"type":35}" data-hovercard="/ajax/hovercard/user.php?id=1116884388" href="https://www.facebook.com/profile.php?id=1116884388">G. B.</a> <span class="commentBody" data-jsid="text"><a data-hovercard="/ajax/hovercard/user.php?id=100000717846530" href="https://www.facebook.com/LYMEMJ">Maria</a>, are you still taking Ivermectin? How long do you think you'll need to be on it? How are you feeling lately? Do you feel you're overcoming this disease by treating with anthelmintic meds?</span></span> </div>
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<span style="font-size: large;"><a class="actorName" data-ft="{"type":35}" data-hovercard="/ajax/hovercard/user.php?id=100000717846530" href="https://www.facebook.com/LYMEMJ">Maria LymeDisease</a> Yes and no and yes. I was taking it every week, feeling better every day. Decided to stop it after a year or so to see what happened, getting sicker, swelling and not good; needed to know if I was "cured" or still needed treatment. Going back to ivermectin tonight. I have "experimented" getting swollen, very sick to my extra limit, then taking the Ivermectin and voila, miracle, doing super good one or two or max three days later... how long? It seems it depends on how infected, invaded the person is. As Dr Phillips (West Palm Beach) said, until every parasite is not expelled or killed there will be Lyme!</span><br />
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<span style="font-size: large;"><abbr class="timestamp livetimestamp" data-date="Wed, 16 Nov 2011 11:23:17 -0800" title="Wednesday, November 16, 2011 at 2:23pm"></abbr><span class="comment_like_496267 fsm fwn fcg" data-ft="{"type":36}"></span>My dose has been just 3 ml a week, imagine that, being functional, living fine, doing many things; of course I still need help to detox,and help for other symptoms like the thyroid or heart but as you know I do not have a Dr nor money so it is what I do with God's help and my beloved Dr who answers my questions by phone. I do think you can overcome Lyme with Ivermectin but not alone, I mean Ivermectin and other medications or herbals or treatments like for example bactrim for the smaller bacteria like Mycoplasma and herbals or supplements!</span> </div>
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<span style="font-size: large;"><a class="actorName" data-ft="{"type":35}" data-hovercard="/ajax/hovercard/user.php?id=1116884388" href="https://www.facebook.com/profile.php?id=1116884388">G. B.</a> Makes me wonder if this battle can ever be won. I haven't read too many people who've been treating parasites say they were "parasite free". Many people who have been on anti parasite meds or herbs for years and still have them. Not very encouraging. Sorry you regressed when you got off Ivermectin, but glad your doing better now that you're on it again. Praying for you!</span><br />
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<span style="font-size: x-large;"><a data-hovercard="/ajax/hovercard/user.php?id=100000717846530" href="https://www.facebook.com/LYMEMJ">Maria LymeDisease</a></span><span style="font-size: large;"><span style="font-size: x-large;"><span style="font-family: Georgia,"Times New Roman",serif;"> </span></span><span style="font-weight: normal;">Lyme is indeed very discouraging lol! Not just saying parasite free, I think it is not bacteria Borrelia free and this one going inside the white blood cells is the one allowing the proliferation of so many other organisms that other wise could be controlled. That is the basic problem; parasites "die easy" but they reproduce in thousands every month if not every day; if the bacteria is there feeding them, and them feeding the bacteria with their "left overs" the problem is much harder to eradicate.</span></span><span style="font-weight: normal;"> </span></h6>
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<span style="font-size: large;"><a class="actorName" data-ft="{"type":35}" data-hovercard="/ajax/hovercard/user.php?id=100000717846530" href="https://www.facebook.com/LYMEMJ"></a> Plus in my specific case, I was diagnosed late, my stronger symptoms started in 2005, I had antibiotics orals sporadically, enough to not die; was dgx in 2009 - the labs showed an acute infection, imagine that, how invaded I was. Continued with oral abx including plaquenil and other that the LLMD gave me and those hurt me more instead of helping, and just after that was when I found the ivermectin thanks to the Colombian Doctor who suspected parasites too. I am sure that if parasites are treated since the beginning, or as soon as possible, Lyme could be eradicated as the malaria is. Do you know malaria could be cured in 3 days? THREE DAYS? I saw my husband recovering from it in three days with a medicine called Fansidar; could this be possible with Lyme but the market prefer to have us sick for interminable years? hope not!</span><br />
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<span style="font-size: large;"><abbr class="timestamp livetimestamp" data-date="Wed, 16 Nov 2011 11:36:25 -0800" title="Wednesday, November 16, 2011 at 2:36pm"></abbr><span class="comment_like_496303 fsm fwn fcg" data-ft="{"type":36}"></span><a class="actorName" data-ft="{"type":35}" data-hovercard="/ajax/hovercard/user.php?id=100000717846530" href="https://www.facebook.com/LYMEMJ"></a> In 2009 my labs showed Borrelia CDC positive; babesia type WA1; and the wet Mount lab showed two more microorganisms "swimming" in my blood, some small round numerous, resembled toxoplasmosis but they said were similar not recognized; the other elongated not as numerous don't know what are those. Imagine someone surviving to just 4 zoonotic infections? this without even been tested for mycoplasma, bartonella, or viruses? so my Colombian Dr said do not take antimalarials could make you sicker, so I stoppped the Plaquenil the LLMD sent me, never went to see him again; and then started Ivermectin in 2010 I guess?</span> </div>
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<span style="font-size: large;"><a class="actorName" data-ft="{"type":35}" data-hovercard="/ajax/hovercard/user.php?id=100000717846530" href="https://www.facebook.com/LYMEMJ"></a> Imagine if instead any of the first TEN doctors i saw would have given me Ivermectin? I saw family practitioners, Infectious Disease specialists; Endocrinologists, heart specialist; another four more family ones; even Drs to whom I worked for free as a medical interpreter.. what if instead of not treating me at all one would have given me Ivermectin for a couple of months? lol ... <b style="background-color: #38761d;">Ignorance is not bliss!</b></span><br />
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<span style="font-size: large;">Many friends here are trying the Ivermectin, most write me sentences saying something like: this is weird, I am feeling fine!! lol! Seriously!!! It is like not feeling exploding inside anymore, like the chest is not ripping apart, like your cells are part of your body again!</span></div>
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<span style="font-size: large;">Let me clear that I started to get sick three months after I stopped Ivermectin and had no other medicines at all, something I wasn't able to have in years, before, anytime i stopped the antibiotics, in two days I was in the deepest sickest place; my swelling now started after three months, so this is great news.</span><br />
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<span style="font-size: large;"><label class="deleteAction stat_elem UIImageBlock_Ext uiCloseButton" for="urrvzd_1"></label> <span class="commentBody" data-jsid="text">My Dear friend F. K. just called to to say that when people asks her about for how long her son Bobby needs to be treated she responds, who ask a diabetic for how long he needs to take insulin? Lyme Disease needs to be treated as long as there is infection! Yes Mam!</span></span><span style="font-size: large;"><abbr class="timestamp livetimestamp" data-date="Wed, 16 Nov 2011 11:50:12 -0800" title="Wednesday, November 16, 2011 at 2:50pm"></abbr><span class="comment_like_496336 fsm fwn fcg" data-ft="{"type":36}"></span></span><br />
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<a href="https://www.facebook.com/profile.php?id=1414597657">E. F.</a> Side effects of Ivermectin. Where do you get this stuff? <br />
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<span style="background-color: #ead1dc;">PD R:</span> Maria I asked my mom about getting a doc in Ecuador to send me ivermectin; but supposively u can get horrible nuero side effects that can be irreversible ; any experience with this ??? <br />
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<span style="background-color: #b4a7d6;">D R</span> Makes me happy I followed my gut instincts and said no to most all treatments. Artemisinin did wonders for me <br />
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<span style="background-color: #d5a6bd;">PDR</span> Ms Dana How did you dose Artemisinin ?? that's an herbal right ?? <br />
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<a href="https://www.facebook.com/LYMEMJ">Maria LD</a></span><span style="font-family: inherit;"> </span><span style="font-family: inherit; font-size: large;"> Dear Dana sorry to tell you Artemisin as the other anti-malarials work in the immune system and suppress it, in fact, this is the reason why I am getting sicker dear G B; I started a couple of days ago a herbal medicine made from "Sacred medicine Sanctuary" that contains Artemisa Annnua, oh God, and the more I took it the more swollen I get... this is kind of funny, me writing to everyone to not take antimalrials and taking it and getting sicker by the minute. Yes, back to ivermectin tonight! <br />
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Maria LDSo just to clear this up, I am swollen not because I stopped the Ivermectin but because I started a treatment with Artemisa annua, precisely what I was posting to not do I was doing, oh yeah, live and learn; thank God I found out on time, I'm about to explode!! Where is my Ivermectin caramba lol! </span> <span style="font-family: inherit; font-size: large;"><br />
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Maria LD: E F and P D R by the contrary Ivermectin seems to be a helper with the neurological infection; it is an anthelmintic made to kill parasites and protozoans; Lyme is a bacteria Borrelia that goes intracellular, especially inside the white blood cells - parasitic?; - the Babesia is a parasite inside the red blood cells, in fact two parasites jump inside the red blood cells at the same time, double worse than the malaria; so, if we must not get anti-malarics because those work by immunesuppression, what to take? anti-parasitics, antifilarials andti-protozoans than won't hurt the immune system nor the Central Nervous system. I have taken Ivermectin for more than a year, small doses and it has been a blessing, by the contrary the Bells Palsy and the neurological symptoms are gone! (The Dr has the Bells Palsy registered in my record, but I don’t have it anymore nor even a small twist in my face!) God is big!</span><span style="font-family: inherit;"> </span><span style="font-family: inherit; font-size: large;"><br />
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These are my opinions and my conversations with my friends!<span style="font-size: large;">I hope they are of some help to others suffering not knowing what is going on! <span style="font-size: large;"> It is not a medical advice nor inte<span style="font-size: large;">nds to replace any medical inf<span style="font-size: large;">ormation.</span></span></span></span></span><br />
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<span style="font-size: large;"><b><span style="font-size: x-small;">NOTE: LYME THE ROLLERCOASTER BLOG DOES NOT OFFER, DOESN'T GIVES<span style="font-size: x-small;">, </span> NOR INTENDS TO GIVE ANY MEDICAL ADVISE NOR MEDICAL RECOMMENDATIONS.</span> </b></span><br />
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MJhttp://www.blogger.com/profile/16614021020877246061noreply@blogger.com0tag:blogger.com,1999:blog-9207742591307790987.post-54242425176377056262011-10-26T03:24:00.000-07:002011-10-26T03:50:48.756-07:00LYME DISEASE, AYUDA A LA ORGANIZACION MUNDIAL DE LA SALUD!<div style="font-family: Verdana,sans-serif;"><span style="font-size: x-large;">Si no son ustedes, entonces ahora quien podra ayudarnos?</span></div><div style="font-family: Verdana,sans-serif;"><span style="font-size: x-large;">Como tengo Lyme Disease, Babesia, Bartonella y otras co-infecciones le escribi pidiendo ayuda a unos medicos muy especializados de mi pais Colombia, eminencias en enfermedades infecciosas, parasitarias y enfermedades Tropicales, pero me respondieron diciendo que era raro tener varias infecciones al mismo tiempo que la Borreliosis transmitida por la picadura de la garrapata. Esto lo dicen basados en sus libros, con el debido respeto, polvorientos y desactualizados porque la realidad que vive el planeta es otra bien diferente y dura, por lo cual apelo a todos quienes puedan aportar de una u otra manera y a la OMS -WHO por sus siglas en ingles- a que nos ayuden a encontrar tratamientos oportunos y adecuados. Esta es mi carta de respuesta y de pedido de ayuda a los medicos y cientificos quienes quisieran reconsiderar sus conocimientos sobre el Lyme Disease:</span></div><div style="font-family: Verdana,sans-serif;"><span style="font-size: x-large;"><br />
</span></div><div style="font-family: Verdana,sans-serif;"></div><div class="MsoNormal" style="color: #cccccc; font-family: Verdana,sans-serif; line-height: normal;"><span style="font-size: x-large;">Lastimosamente no soy ni la primera ni la ultima en tener mas de una co-infeccion sumada a la Borrelia, por el contrario al parecer solo los Europeos parecen ser quienes no tienen tales co-infecciones. Peor aun aqui en USA la lista de co-infecciones como resultado de la picadura de la garrapata parecen ser interminables en un mismo individuo, nombres como Babesia, Bartonella, Mycoplasma, tularemia, Erlichia, Rickettsia, infecciones filariales tipo Ceguera del Rio, tipo toxoplasmosis y muchas otras son nuestro dia a dia. No soy la excepcion. Ver cuadro:</span></div><div class="MsoNormal" style="background-color: #d9ead3; color: #cccccc; font-family: Verdana,sans-serif; line-height: normal;"><span style="font-size: x-large;"><a href="http://www.lymedisease.org/lyme101/coinfections/tick_chart1.html">http://www.lymedisease.org/lyme101/coinfections/tick_chart1.html</a></span></div><div class="MsoNormal" style="color: #cccccc; font-family: Verdana,sans-serif; line-height: normal;"><span style="font-size: x-large;"><br />
</span></div><div class="MsoNormal" style="color: #cccccc; font-family: Verdana,sans-serif; line-height: normal;"><span style="font-size: x-large;">Y una frase sobre co-infecciones del Dr Klinghardt quien tiene mucho exito tratando el Lyme aqui en USA:</span></div><div class="MsoNormal" style="color: #cccccc; font-family: Verdana,sans-serif; line-height: normal; margin-bottom: 0.0001pt;"><span style="font-size: x-large;">"It is our experience that most Lyme patients, by the time the infection has become chronic, have multiple parasites in their bowel. Co-infections from the herpes virus family, Coxsackie's viruses, influenza viruses, echo viruses and the measles virus seem to be common. Frequently they also have one of several mycoplasma species present and a multitude of other bacterial infections. Fungi always thrive in a Lyme-infected patient. The treatment therefore needs to be broad based and address all these co-infections in order to succeed. <span style="background-color: #38761d;">Treatment for Lyme disease is often unsuccessful when it targets only the Lyme spirochete but not the existing co-infections</span><span style="background-color: #38761d;">."</span></span></div><div class="MsoNormal" style="color: #cccccc; font-family: Verdana,sans-serif; line-height: normal; margin-bottom: 0.0001pt;"><span style="font-size: x-large;">Osea, esto no es un invento mio!</span></div><div class="MsoNormal" style="color: #cccccc; font-family: Verdana,sans-serif; line-height: normal;"><span style="font-size: x-large;">Por eso les escribi, porque ustedes pueden conocer estas infecciones mas que los medicos de aqui y pueden saber tratarlas.</span></div><div class="MsoNormal" style="color: #cccccc; font-family: Verdana,sans-serif; line-height: normal;"><span style="font-size: x-large;">solo por confirmar lo que digo copio aqui una frase del blog del Dr J., quien fue quien el medico quien me diagnostico en</span></div><div class="MsoNormal" style="color: #cccccc; font-family: Verdana,sans-serif; line-height: normal;"><span style="font-size: x-large;">el 2009: "A large percent of patient have the BBB triad: Borrelia, Bartonella, Babesia." Osea la mayoria minimo tenemos la triada BBB, ademas que ya encontraron Mycoplasma y filarial como una constante: Esto lo dijo en el Doctor en el 2010, aqui su blog completo: </span></div><div class="MsoNormal" style="background-color: #d9ead3; color: #cccccc; font-family: Verdana,sans-serif; line-height: normal;"><span style="font-size: x-large;"><a href="http://lymemd.blogspot.com/2010/01/lyme-2010-brief-update.html">http://lymemd.blogspot.com/2010/01/lyme-2010-brief-update.html</a></span></div><div class="MsoNormal" style="font-family: Verdana,sans-serif; line-height: normal;"><span style="font-size: x-large;"><a href="http://lymemd.blogspot.com/2010/01/lyme-2010-brief-update.html"><span style="color: blue;"><br />
</span></a></span></div><div class="MsoNormal" style="font-family: Verdana,sans-serif; line-height: normal;"><span style="font-size: x-large;">Ya esto es reconocido por muchos medicos en USA y como les dije es el dia a dia de nosotros los pacientes,</span></div><div class="MsoNormal" style="font-family: Verdana,sans-serif; line-height: normal;"><span style="font-size: x-large;">quienes tenemos que sobrevivir a las muchas co-infeccines; no son casos aislados ni raros, es lo "comun". Hay muchisima literatura medica al respecto que bien les puedo enviar si les interesara. Es tanto asi que se habla de una "arma biologica" por la multiplicidad de infecciones bacteriales, parasitarias, viruses y hasta hongos todas al mismo tiempo; es decir, los libros tradicionales medicos sobre Lyme Disease estan desactualizados y desinformando a los mismos medicos. Repito por eso estoy buscando ayuda de personas mas expertas en infecciones y que puedan considerar la importancia y gravedad del asunto. No por mi o para curarme a mi, solo por sembrarles la semilla de la duda de lo que se avecina o que ya llego.</span></div><div class="MsoNormal" style="font-family: Verdana,sans-serif; line-height: normal;"><span style="font-size: x-large;"><br />
</span></div><div class="MsoNormal" style="font-family: Verdana,sans-serif; line-height: normal;"><span style="font-size: x-large;">3. Las investigaciones de la Doctora Eva Sapi, aqui en USA; y las investigaciones de los primos Boronson en Noruega han mostrado resultados altamente positivos para eradicar la Borrelia con Tinidazol o Tindamax, y han hecho estudios con Flagyl y otros; esto porque la Borrelia toma muchas formas y no es posible de controlarla solo con antibioticos como se decia anteriormente; se habla de quistes, de biofilms y de muchas formas que toma la bacteria para evadir los ataques y por ello se investigan tratamientos diferentes, entre ellos se ha hecho mucho enfasis en el uso de antimalaricos como la hierba Artemisia o la llaman Artemisinin tambien. La Dra Sapi ha retomado los estudios del Dr Burgdorferi -descubridor de la Borrelia en los ticks- y encontro que las garrapatas estas tienen no solo la bacteria Borrelia, sino Mycoplasma y unos protozoarios filariales; dice ella que de ser confirmados requeririan tratamientos antifilariales, palabras textuales. En mi experiencia la Ivermectina me salvo la vida, pero imagino mi experiencia no dice mas que lo que digan los libros o los cientificos. Aqui copio un enlace del video de la Dr Sapi cuando habla de sus hallazgos: </span></div><div class="MsoNormal" style="background-color: #d9ead3; font-family: Verdana,sans-serif; line-height: normal;"><span style="font-size: x-large;"><a href="http://www.youtube.com/watch?v=AmvgOfIN_8c"><span style="color: blue;">http://www.youtube.com/watch?v=AmvgOfIN_8c</span></a></span></div><div class="MsoNormal" style="font-family: Verdana,sans-serif; line-height: normal;"><span style="font-size: x-large;"><br />
</span></div><div class="MsoNormal" style="font-family: Verdana,sans-serif; line-height: normal;"><span style="font-size: x-large;">Y este es un enlace otra vez del Dr J cuando habla de tratamientos con Tindamax o Tinidazol para mostrarles que los antiparasitarios son casi que obligatorios ya para tratar el Lyme: - les cuento que cuando yo hable con el personalmente sobre Flagyl, Bactrim o antiparasiticos este Doctor casi se me rie en la cara, me dijo "no trato con antiparasiticos y esta demostrado que no sirven en Lyme Disease"; esto fue en el 2009, hoy pueden leer su blog cuando afirma lo opuesto:</span></div><div class="MsoNormal" style="font-family: Verdana,sans-serif; line-height: normal;"><span style="font-size: x-large;">"I cannot cover the whole Sapi study. The most exciting finding is that Tindamax (tinidazole) - our premier Cyst-buster, is the most effective drug overall. This "cyst-buster" kills 90% of cysts and spirochetes: by far the best drug. We don't know it's effect on L-forms, but we can guess. Tindamax probably works by an intracellular mechanism. If this is true it should be equally effective against L-forms. It gets even better. Tindamax is the only drug which does a great job on biofilm colonies as well! (not to be discussed now). More on biofilms later. <span style="background-color: #38761d;">Tindamax passes the blood brain barrier and penetrates well into most tissues. It has been effective in my patients with neurocognitive deficits - neuroborreliosis."</span></span></div><div class="MsoNormal" style="font-family: Verdana,sans-serif; line-height: normal;"><span style="font-size: x-large;"><br />
</span></div><div class="MsoNormal" style="background-color: #b6d7a8; font-family: Verdana,sans-serif; line-height: normal;"><span style="font-size: x-large;"><a href="http://lymemd.blogspot.com/2011/07/everything-you-thought-you-knew-about.html"><span style="color: blue;">http://lymemd.blogspot.com/2011/07/everything-you-thought-you-knew-about.html</span></a></span></div><div class="MsoNormal" style="font-family: Verdana,sans-serif; line-height: normal;"><span style="font-size: x-large;"><br />
</span></div><div class="MsoNormal" style="font-family: Verdana,sans-serif; line-height: normal;"><span style="font-size: x-large;">Lo que quiero traerles es lo que estamos viviendo los enfermos de Lyme Disease, una constelacion de sintomas ademas incurables, enfermedades interminables sin respuestas concretas, con tantas negaciones y tantos obstaculos que deberian ser resueltos por el bien de la humanidad para evitar esto se propague y convierta en una pandemia sin limites. Ustedes son los llamados a considerar la importancia de esta infeccion, llamese nueva o desconocida y buscar formas de tratamiento que eviten la propagacion y el sufrimiento de los pacientes. como les digo, tengo 700 amigos en Usa y en Europa y Sur Africa, todos viviendo esto que yo vivo todos los dias, con problemas neurologicos, del sistema linfatico, cardiacos, y tantos sintomas hasta tener animalitos saliendonos por la piel. Aqui hay muchos Doctores haciendo tratamientos con multiples antibioticos intravenosos al mismo tiempo y ya muchos empezaron a investigar la posibilidad de usar anthelminticos. Hay un medico muy reconocido en Europa y ahora qui en USA quien se llama Dr Klinghardt. El se ha dedicado a tratamientos de Lyme Disease y usa medicinas tradicionales y suplementos con hierbas y otros tratamientos poco cnvencionales. Entre los muchos metodos que utiliza, solo para que vean la parte donde trata con antiparasitarios, en su "protocolo", noten que combina Pamoato de Pyrantel con Ivermectina, utiliza Nitaxozanida, Praziquantel y remata con Albendazol; si eso no es lo correcto entonces por que dice que tiene tantos casos con logros que no tienen la mayoria de los medicos tradicionales? </span></div><div class="MsoNormal" style="background-color: #d9ead3; font-family: Verdana,sans-serif; line-height: normal;"><span style="font-size: x-large;"><a href="http://www.klinghardtacademy.com/Lyme-Disease/"><span style="color: blue;">http://www.klinghardtacademy.com/Lyme-Disease/</span></a></span></div><div class="MsoNormal" style="font-family: Verdana,sans-serif; line-height: normal;"><span style="font-size: x-large;"><br />
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</span></div><div class="MsoNormal" style="font-family: Verdana,sans-serif; line-height: normal;"><span style="font-size: x-large;">A ustedes les pido de corazon que investiguen sobre el Lyme Disease y que por su condicion de investigadores y profesores emeritos, Directores de entidades Nacionales de enfermedades Tropicales e infecciosas y miembros o participantes de la Organizacion Mundial de la salud, de encontrar validez en mi investigacion, alerten y generen proyectos para controlar, tratar adecuadamente y de ser posible eradicar esta infeccion que esta dejando cuadraplegicos y con demencia a quienes no se tratan debidamente; es una enfermedad dificil de diagnosticar y de tratar y se sufre largamente con ella, asi es que de ustedes depende el escuchar el clamor de quienes ahora necesitan de sus conocimientos y sus practicas cientificas y medicas para el beneficio de todos.</span></div><div class="MsoNormal" style="font-family: Verdana,sans-serif; line-height: normal;"><span style="font-size: x-large;"><br />
</span></div><div class="MsoNormal" style="font-family: Verdana,sans-serif; line-height: normal;"><span style="font-size: x-large;">Esta carta la hare publica sin presentar sus nombres para no comprometerlos, pero para hacer el llamado a todos quienes crean que de alguna manera puedan ayudar con esta infeccion que esta azotando a los paises mas desarrollados los cuales por su condicion de super potencias la niegan o esconden para detrimento del mundo entero y de las personas que la estan sufriendo. Apelo a su conocimiento y a su compasion.</span></div><div class="MsoNormal" style="font-family: Verdana,sans-serif; line-height: normal;"><span style="font-size: x-large;"><br />
</span></div><div class="MsoNormal" style="font-family: Verdana,sans-serif; line-height: normal;"><span style="font-size: x-large;">Muchas gracias</span></div><div class="MsoNormal" style="font-family: Verdana,sans-serif; line-height: normal;"><span style="font-size: x-large;"><br />
</span></div><div class="MsoNormal" style="line-height: normal; mso-margin-bottom-alt: auto; mso-margin-top-alt: auto;"><span style="font-family: Verdana,sans-serif; font-size: x-large;">MPJ.</span><br />
<span style="font-family: Verdana,sans-serif; font-size: large;"><span style="font-size: x-large;">Enferma de LD y Periodista Colombiana</span>. </span></div>MJhttp://www.blogger.com/profile/16614021020877246061noreply@blogger.com0tag:blogger.com,1999:blog-9207742591307790987.post-21016470264661596722011-08-28T18:31:00.000-07:002013-02-27T22:40:37.853-08:00LYME DISEASE; TREATING BABESIA WITH ANTHELMINTICS<div class="MsoNormal" style="text-align: justify;">
<span style="font-family: "Arial","sans-serif"; font-size: large; line-height: 115%;">A friend of a friend asked me about <span style="font-size: large;">what treatment did I use for </span>for Babesia because his Doctor gave him one week of Mepron and refuses to treat him longer; the friend of my friend thinks one week of treatment is not enough and is searching to get other possible treatments. This is my answer:</span></div>
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<span style="font-family: "Arial","sans-serif"; font-size: large; line-height: 115%;">“I guess E. told you to contact me because we have spoken before about ways to treat the parasites. As you might know Babesia is a big parasite that travels inside the red blood cells, imagine that, a bug living out of our life resource, so of course the anemia is huge and the symptoms are many. I found Babesia to be worse than malaria because the parasites of the malaria go inside the red blood cell but one at a time, the Babesia seems to be a gringo malaria smarter and stronger because two and sometimes three bugs go inside each red blood cell; "Babesia bigemina"? Means two! This is not to scare you but to show why it is indeed vital to treat it and as long as it is needed.</span></div>
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<span style="font-family: "Arial","sans-serif"; font-size: large; line-height: 115%;">I am Hispanic, so I always heard about treating parasites in my home country, and then I traveled and lived in an area that was endemic of malaria, so this topic is not new to me, what surprises me is to find it here in the US where in theory there are <u><span style="font-size: large;"><b>"</b></span>no parasites" in the US, </u> and of course no infections of this type like in South America or Africa. </span><br />
<span style="font-family: "Arial","sans-serif"; font-size: large; line-height: 115%;">So in my case living in Florida, after many Doctors and tons of not knowing what was wrong with me and after lots of suffering and finally treating with antibiotics for long time and not recovering I called my former family physician in Colombia and he remembered me and helped me by phone and all I am going to tell you and what I write in my blog is based on his teaching and my researching meaning, I am not an expert, nor the wise one here, just a friend willing to share and help if I can; at least I try.</span></div>
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<span style="font-family: "Arial","sans-serif"; font-size: large; line-height: 115%;">The one thing about your case that calls my attention and I have seen here a lot is, why Drs do not re-test? Your Doc treated you, thank you, but he won't re-test to see if his treatment worked? Who he thinks he is? God? Or his treatment is the ultimate cure? Really?</span></div>
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<span style="font-family: "Arial","sans-serif"; font-size: large; line-height: 115%;">To the point - finally sorry -</span></div>
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<span style="font-family: "Arial","sans-serif"; font-size: large; line-height: 115%;">I have been taking Ivermectin - this is an anthelmintic, meaning anti-parasitic. There are many medicines of this type, Flagyl, Tindamax and even herbs and garlic are part of the group (see in the bottom from Wikipedia the definition and types of anthelmintics). The difference with Ivermectin is that this drug started as a veterinarian medicine - and if you permit me my opinion, medicines made for animals are made to cure them; the ones for us are made to keep us going to the Dr and taking more medicines to fill their pockets.</span></div>
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<span style="font-family: "Arial","sans-serif"; font-size: large; line-height: 115%;">Seriously, it was a veterinary medicine and then used in humans and after twenty years or more using it in South America and in Africa the US is starting to use it. In most parts it is used as antiparasitic and in Africa not only as anti-malarial but also to treat "filarial infections" such as "Onchoneriasis" or also called "River blindness". As long as I've heard Mr. Burgdorferi said the ticks transmit a bacterium called Borrelia and also some protozoans of the filarial type<span style="font-size: large;">; of course the medical community doesn't want to hear this and are <span style="font-size: large;">consciously</span> ignoring the filarial infection condemning the patient<span style="font-size: large;">s to not be cured!</span></span> </span></div>
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<span style="font-family: "Arial","sans-serif"; font-size: large; line-height: 115%;">For all this the Ivermectin seems to be the medicine to treat us, both filarial infections and Babesia. But that is not all. My Dr told me that Ivermectin was found to not hurt the Central Nervous system as many of the anthelmintics do; plus, he didn't want me to take regular antimalarials because those act by immune suppression and me, we, Lymies have multiple infections bacterial and parasitic that could be free of growing if there is immune suppression. So again my Dr recommended me to take Ivermectin to begin with. He said that if I needed to combine it, or to altern it from time time time I cou<span style="font-size: large;">ld take </span>Alinia was his second drug of choice, again because it seems to not hurt the Central Nervous system as much. In my country Albendazole is very used to treat malaria and parasites, but he preferred me to not take it if I could have Ivermectin instead or Alinia -Nitaxozanida. The "Albenda" as many call it her in the US was found to hurt the CNS to the point children were showing symptoms similar to Parkinson's. But a short treatment is good, not the long one intended for me.</span></div>
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<span style="font-family: "Arial","sans-serif"; font-size: large; line-height: 115%;">So how to take the Ivermectin? after seeing my labs my Dr said I had so many infections running at the same time and so many of them being parasitic, I must start very low in the treatment and do it for long time. He said the strong treatments are better for the acute infections and when the patient is not that invaded yet. By "invaded" I mean the parasites can lay from 250 to 250,000 eggs even per day, week or month, so the more they reproduce and travel around the body the sicker we are - invaded I mean! My Dr said the toxins the parasite release are the ones that make us sicker even more than having he parasite eating us alive, these toxins are released in bigger amounts when the bugs die (their poop in clear words); also the medicine itself to be able to kill parasites is a big toxin (now we are talking about two time toxicity when killing parasites), and the last third big toxin load we get is the bodies of the dead parasites, imagine these creatures dead and our body trying to get rid of them. We need good bacteria to come eat these dead bodies –debris-, and we need to eat papaya and good digestive enzymes to help the belly and digestive process and then we need to detox with treatments like enemas and colonics to kick them out. Also Castor oil and Milk of magnesia help a lot!</span></div>
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<span style="font-family: "Arial","sans-serif"; font-size: large; line-height: 115%;">Yes my first treatment was truly strong, I thought I was stronger than those bugs and I could kill them before they could kill me so i took a higher dose.. Of course I was wrong, lol, got so sick that I had to call my Doc and he almost yell at me: cut the dose in half and keep it long time, 3 to six months before considering to raise it to your regular dose; and that I did. <span style="font-size: large;">I've been taking it once a week long time!</span></span></div>
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<span style="font-family: "Arial","sans-serif"; font-size: large; line-height: 115%;">Which is the dose? the Ivermectin sold in SA is a little bottle like tear drops and the dose is one drop per one kilogram ONCE A WEEK in my case due to my overload; meaning it is a dose according to each one's weight and condition, and it is not given daily due to the medicine stays in the body four days. So if I was supposed to take 50 drops I started with 25 and just around the first year I was taking the dose for me. I kept my antibiotics until I was able to not take them anymore, and I do probiotics and eat papaya every day and try to take some care eating without sugar nor carbs.</span></div>
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<span style="font-family: "Arial","sans-serif"; font-size: large; line-height: 115%;">After all my meds from my home country were finished I looked for options here in the US. I found the Ivermectin here is called "Stromectol" comes in pills, boxes of 3 or 6 pills and it is very expensive. I guess these pills must be of a lesser concentration than my liquid human version because I found some Drs here, well Dr K who comes from outside of the US, gives 12 mgs a day and sometimes he gives 12 mgs three times a day for two weeks and to some patients he has given them this "megadose" every day for one month? I called my Dr and asked for his opinion. He was the one that concluded that probably the pills were less concentrated and could be given in such amounts. The dose I've taken is barely 3 mgs once a week, and I have not had any bad reaction and I can talk about recovering. So Stromectol is one human version in pills. Ivermectina gotas the human in drops bottles of 6 ml. The other option is Ivomec<span style="font-size: large;">, injectable</span> ( for cows) but people in the rural areas of <span style="font-size: large;">my country swallow it in small doses for the malaria. I learn<span style="font-size: large;"> in the US this is considered a illeg<span style="font-size: large;">al idea so, just for information purp<span style="font-size: large;">oses as where it is taken and how much. </span></span></span></span></span></div>
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<span style="font-family: "Arial","sans-serif"; font-size: large; line-height: 115%;">(Due to I have to buy everything out of pocket and help myself with God's help, I looked for more alternatives and asked my Dr about the veterinary versions of Ivermectin. -My husband's relatives told me that the people living in the endemic areas injected themselves with "Ivomec" the Ivermectin made for cattle; they used one cm for 50 KILOS of weight. - Well, my Dr said this medicine is as good as the human one and could be taken orally too. He said he preferred the oral method to be able to control the dose according to the weight, and better absorption of it. I found the Ivomec very cheap in the internet but I think I don't have four stomachs as the cows do, so I looked into horse medicine because we all know these animals are the most expensive and the medicine for them is the very best. I found many versions of horse Ivermectin for just $4.99 and it called my attention one product called "Zimectrin Gold" because it contains Ivermectin and also "Praziquantel" another anthelmintic used for bigger bugs including treating for flukes which I suspect I have and many Lymies have found to have too. I bought it for $13.99 a tube with higher concentration and with the amount for a horse of 1,250 pounds, meaning I found medicine for long term treatment at a price I could certainly afford. I called my Doc again and he told me to reduce the dose to the half of the horse dosing. So I take max the amount marked for 100 pounds if I weigh 200. One thing you must know, this medicine is the bitterest nasty of the planet. I put the little amount of paste in a spoon, and then I grab it with my finger and put it deep inside my throat and then swallow it with water and try to eat some peanut butter or anything to pass that taste. But listen, my Dr told me to have Ivermectin with the stomach empty, not meaning fasting but for example before going to sleep, two hours after my last meal. This I did once a week and after feeling so good I stopped all medicines for a month, then tried another one called Triventor because this one has "Triclabendazole" to treat the flukes and just took two doses in two days and have not had any treatment since this two months ago and I pray thanking God every day I feel better and recovering! Is this the cure? I don't know, cannot tell yet; plus my heart and my body are still very battered after six years of antibiotics and extreme illness so I still won't sing victory, but yes I am feeling well.)</span></div>
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<span style="font-family: "Arial","sans-serif"; font-size: large; line-height: 115%;">I share my experience and all my thoughts in my blog hoping to bring some light to others - many- who could be as desperate as I was after being so sick and the sicker I was the more Drs dismissed me. I'm not saying take this medicines nor do as I did, just research and find out that Lyme Disease is also a parasitic infection and we will continue to be sick if Drs don't treat the parasites that came with the tick bite, I don't mean only the regular intestinal parasites but parasites in our blood inside our red blood cells, inside the white blood c<span style="font-size: large;">ells and inside our tissues, organs and everywhere! </span></span><br />
<span style="font-family: "Arial","sans-serif"; font-size: large; line-height: 115%;"><span style="font-size: large;"><b><span style="font-size: large;">D</span></b></span><b>enying the parasitic infection that comes from a vector borne infection is the most cruel ignorance of the medical field in the US.</b></span></div>
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<span style="font-family: "Arial","sans-serif"; font-size: large; line-height: 115%;">I pray for Dr J in Maryland who diagnosed me and for my Dr JQP who takes my phone calls. I have no words to thank my family for sending me so many medicines and to all who help me here; but my reason of doing all I do is to help my Lymie friends because there has to be light out of this tunnel and it looks like I found a piece of this puzzle I need to share, for free with no commercial obligations nor compromises. <b>Yes take antibiotics as needed but to recover from Lyme Disease and Babesia you do need anthelmintics.</b> My thinking. </span><br />
<span style="font-family: "Arial","sans-serif"; font-size: large; line-height: 115%;">May God guide me to say and do what is correct every day amen. May God guide you to do what you need to do to recover and heal. I pray for your recovery and hope to share this light with love and happiness, wooo hooo, to recovery we go!</span></div>
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<span style="font-family: "Arial","sans-serif"; font-size: large; line-height: 115%;">Hugs and big hugs to my friend E!!!!!!!!!!!!!</span><br />
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<span style="font-family: "Arial","sans-serif"; font-size: large; line-height: 115%;">Note: </span><br />
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EGCG</span></h1>
<span style="font-family: "Arial","sans-serif"; font-size: large; line-height: 115%;">Would like to add a link to a great information my friend CH just sent me, it is a study made in Japan that shows that patients who received this medicine taken from the green tea <span style="font-family: Times,"Times New Roman",serif;">"</span></span><span style="font-family: Times,"Times New Roman",serif; font-size: large;"><b>significantly (P<0.05) inhibited the growth of B. microti at doses of 5 and 10 mg/kg body weight, and the parasites completely cleared on day 14 and 16 post-inoculation in the 5 and 10 mg/kg treated groups, respectively. These findings highlight the potentiality of (-)-Epigallocatechin-3-gallate as a chemotherapeutic drug for the treatment of babesiosis.</b></span><span style="font-family: Times,"Times New Roman",serif; font-size: large;"><b> </b></span><br />
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<span style="font-size: large;"><b>Thank you all for sharing all these with me!!!</b></span><br />
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<span style="font-size: small;"><b>http://en.wikipedia.org/wiki/Babesiosis<a href="http://en.wikipedia.org/wiki/Babesiosis">http://en.wikipedia.org/wiki/Babesiosis</a></b></span><br />
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<span style="font-size: large;"><b>MARIA.</b></span><br />
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<span style="font-size: large;"><b><span style="font-size: x-small;">NOTE: LYME THE ROLLERCOASTER BLOG DOES NOT OFFER, DOESN'T GIVE<span style="font-size: x-small;">, </span> NOR INTENDS TO GIVE ANY MEDICAL ADVISE NOR MEDICAL RECOMMENDATIONS.</span></b></span><span style="font-size: small;"><b> </b></span></div>
MJhttp://www.blogger.com/profile/16614021020877246061noreply@blogger.com0tag:blogger.com,1999:blog-9207742591307790987.post-75797546730145131602011-08-05T05:22:00.000-07:002011-08-05T06:50:35.807-07:00LYME DISEASE: LA ENFERMEDAD DE LA GARRAPATA, TIENE CURA?<div style="text-align: justify;"><span style="font-family: "Times New Roman","serif"; font-size: x-large;">Mi amiga periodista me pregunta como sobrevivo a la enfermedad de la garrapata y si tiene cura? </span></div><div style="text-align: justify;"><span style="font-family: "Times New Roman","serif"; font-size: x-large;">(Nota: vivo en Florida y se supone que aqui no decimos "bicho" porque los puertorriqueños se ofenden pues lo consideran una mala palabra que significa el organo masculino? pero para nosotros solo quiere decir animal pequeño o hasta microorganismo, asi es que perdonenme el uso de esa palabra en este mensaje).</span> </div><div class="MsoNormal" style="line-height: normal; margin-bottom: 12pt; text-align: justify;"><span style="font-family: "Times New Roman","serif"; font-size: x-large;"><br />
</span></div><div class="MsoNormal" style="line-height: normal; margin-bottom: 12pt; text-align: justify;"><span style="font-family: "Times New Roman","serif"; font-size: x-large;">Entonces LYME DISEASE - La Enfermedad de la Garrapata tiene o no cura? Esta es mi historia y mi opinion:</span></div><div class="MsoNormal" style="line-height: normal; margin-bottom: 12pt; text-align: justify;"><span style="font-family: "Times New Roman","serif"; font-size: x-large;"><br />
Mi caso es severo como el de muchos aqui y este pais lo niega pues no quieren que se sepa que tienen una enfermedad tipo malaria - peor; si compararamos el parasito de la malaria se mete entre el globulo rojo para vivir alli, luego va al higado y luego al cerebro y termina matando a su huesped. En la enfermedad gringa la picadura es de un garrapatica muy pequeña que no solo transmite una bacteria sino varios tipos de bichos entre bacterias y parasitos y aun no se sabe cuales son todos, solo se le ha dado nombre a algunos y curiosamente no matan al huesped sino solo luego de muchos años largos de sufrimiento... - hay quienes dicen que la garrapatita fue creada como parte de la guerra biologica y se les escapo de su centro de investigaciones de Plum Island? En todo caso por comparar solo uno de ellos, la Babesia es una infeccion donde son tres parasitos los que al mismo tiempo se meten entre el globulo rojo a comer y vivir!! Osea es una triple malaria!!!! Y por su parte la bacteria Borrelia, la base conocida de la infeccion, salta a los globulos blancos, daña el sistema immunologico y viaja entre los globulos blancos por todo el cuerpo para vivir a sus anchas...</span></div><div class="MsoNormal" style="line-height: normal; margin-bottom: 12pt; text-align: justify;"><span style="font-size: x-large;"><br />
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<span style="font-family: "Times New Roman","serif"; font-size: x-large;"> </span></div><div class="MsoNormal" style="line-height: normal; margin-bottom: 12pt; text-align: justify;"><span style="font-family: "Times New Roman","serif"; font-size: x-large;">De la sangre la infeccion viaja a a la base del cerebro y se mueve por entre el sistema linfatico, - son todas las glandulas infectadas - uno de los primeros sintomas es el cuello inflamado, dolor en la base del craneo y tiroides; y desde alli se mueve por las venas al resto del cuerpo y desde las glandulas al cerebro, corazon y demas organos.. los sintomas son entonces perdida de memoria, vision borrosa, sintomas neurologicos como incremento o perdida del olfato y el gusto, incremento en la audicion - supe de una mujer quien sufrio tanto por lo del sonido que llego a suicidarse porque los medicos no le ayudaron durante años hasta que enloquecio.. tambien por la infeccion en el cerebro puede haber depresion clinica o unas iras como la demencia en los casos de sifilis o malaria cerebral... siguen luego sintomas como palpitaciones y arritmias, diarreas agudas, dolores artriticos, los musculos se caen, incremento subito o perdida subita de peso, dolores agudos de cabeza, de piernas, todos los nervios infectados dan unos calambres muy fuertes, o en el riñon o de estomago; estamos hablando artritis y dolores musculares - aqui les dan opiaceas para el dolor, conozco a una mujer que la tratan con 113 medicinas diarias, entre ellas cuatro opiaceas y morfina.. no, ella no es la mas enferma pero si una adicta... conozco otros casos de personas en cama sin levantarse 4 o 5 años... una joven de 24 años quien no logra permanencer sentada mas de 5 o 10 minutos porque se desmaya, despues de cientos de medicos - su familia tiene los recursos - un medico Ingles le encontro parasitos alojados en el sinus, la garganta y el cerebro...? El tratamiento aqui es antibiotico intravenoso a razon de $2,500 por semana o por mes si tiene seguro? osea es el negocio redondo! </span></div><div class="MsoNormal" style="line-height: normal; margin-bottom: 12pt; text-align: justify;"><span style="font-family: "Times New Roman","serif"; font-size: x-large;">El medico que descubrio que la garrapata transmitia una bacteria, Dr </span><span style="font-size: x-large;"><b>Willy Burgdorfer</b></span><span style="font-family: "Times New Roman","serif"; font-size: x-large;">, tambien dijo que habian parasitos tipo filariales como los de la elefantiasis en Africa, o tambien llamada “Ceguera del Rio” o "Onchoneriasis"; pero aqui eso lo cubrieron con tierrita porque entonces estariamos hablando de una enfermedad peor que la malaria y la “Onchoneriasis” ?? eso seria la peor imagen en el mundo. Solo por contarles me toco ver a una amiga con Lyme cuando le salio un bicho por el ojo, pequeñito, y luego empezamos a tomarles fotos y ya tengo un album… quiero decir, es una enfermedad de pelicula de terror que USA esconde!<br />
</span> </div><div class="MsoNormal" style="line-height: normal; margin-bottom: 12pt; text-align: justify;"><span style="font-family: "Times New Roman","serif"; font-size: x-large;">Mi historia empieza desde el 2006. Pase por diez medicos y todos se pasaban la pelota caliente - aqui en la Florida no hay ni puede haber Lyme Disease, imposible! Es una enfermedad que en su ciclo envuelve el paso por la rata y el venado - osea... seria como decir que Mickey y Bambi son transmisiores de una enfermedad casi mortal.. o que aqui no la saben curar? .... pero mi historia es comun, la mayoria de los enfermos con Lyme no solo sufren la terrible enfermedad sino el rechazo y la negacion de la mayoria de los medicos; creo que a los Doctores les da miedo enfrentar a un paciente multisintomatico, multiinfectado, o prefieren usar una evasiva y es mas facil decir que tiene menopausia o alergias? ... me costo $650 dolares el examen que decia que NO era menopausia... ombe si me dolio el bolsillo y el ego... entonces gracias al internet encontre el nombre de la enfermedad que tenia, Lyme Disease, y luego fui a ver especialistas de enfermedades infeccionsas quienes igual lo negaron, "que si tenia alguna infeccion la habia traido de Colombia"? </span></div><div style="text-align: justify;"><span style="font-family: "Times New Roman","serif"; font-size: x-large; line-height: 115%;">y entonces mi Primo me mando antibioticos desde Medellin para ayudarme, pero apenas los paraba me empeoraba; luego gracias a Dios llame a mi medico de la epoca cuando vivimos en Cali - lo llame porque era un medico que iba a la casa a ver a sus pacientes muy sabio, muy estudioso y muy compasivo - y claro Dr J Q sabia mas de infecciones bacteriales y parasitarias que los medicos de aqui y me empezo a tratar por telefono primero la tiroides, me dio otros antibioticos pero cuando se me acababan yo empeoraba hasta no poderme mover para ir al baño… luego de muchos meses sin mejorar al Doctor se le ocurrio intentar tratamiento antiparasitario? Aqui las entidades medicas especializadas decian que ni el Bactrim ni el Flagyl servian para tratar esta enfermedad. Yo empece con Metronidazol y no solo senti mejoria sino que por primera vez note algo de recuperacion, pero la infeccion aun era brutal.. entonces en el 2009 fui a ver a un medico en Maryland, ya fui capaz de viajar! Este Doctor con solo verme reconocio varios sintomas como el "Bells Palsy" que es paralisis de un lado de la cara como si hubiera tenido un derrame, y miro mi cuello y la dificultad para tragar y el corazon, etc... me mando examenes de sangre para confirmar su diagnostico clinico: Lyme Disease! y me dio antibioticos! ... Le rogue me hicieran un examen para ver si tenia parasitos intestinales pero no.. el Dr no trata parasitos... pero si llevo tres años con daño de estomago please... los examenes mostraron que tenia la famosa bacteria Borrelia, tambien el parasito Babesia y que en mi sangre habian otros dos parasitos que no lograron saber que eran? uno redondo muy numeroso tipo toxoplasmosis y otro alargado con bolitas en las puntas? ... osea, para empezar 4 tipos de bichos sin examenes exhaustivos solo los basicos? </span> </div><div class="MsoNormal" style="line-height: normal; margin-bottom: 12pt; text-align: justify;"><span style="font-size: x-large;"><br />
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Mas me hubiera valido "coger" una malaria cuando me fui a vivir a la selva de Bahia Solano que esta infeccion gringa...<br />
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</span><span style="font-family: "Times New Roman","serif"; font-size: x-large; line-height: 115%;">No tenia dinero para regresar a Maryland y el Dr no me iba a tratar por telefono; las inyecciones de penicilina me costaron $1,200 dls, cada 20 pastillas me valian $300 y era una lista interminable de gastos, sin decirles que los medicos especializados cobran $875 por la consulta y si es alguna preguntita telefonica cobran $10 por minuto? .. gracias a Dios mi familia me mando medicinas y aun cada vez que alguien viaja me traen medicinas y con eso me salvaron la vida - Dios les pague! </span><span style="font-family: "Times New Roman","serif"; font-size: x-large;">... pero que conste que no me estoy quejando ni mas faltaba, solo era para que vieran como es la atencion medica en USA; antes a mi me ha ido super bien porque las personas que conozco con LD se gastan entre 40 y 60 mil dolares en su tratamiento anual y aun siguen muy enfermos o recaen constantemente.. yo no me quejo, por el contrario mi familia me ha enviado tantas medicinas de Colombia que tengo un arsenal repleto; pero la gran diferencia ha sido ese medico Caleño quien me dio <b>Ivermectina</b>... siii, la medicina que empezo como Ivomec para purgar el ganado? muuu, me salvo la vida!!!! No, no es un comercial!!! Si no hay tratamiento antiparasitario no hay recuperacion en el Lyme Disease, digo yo!</span></div><div class="MsoNormal" style="line-height: normal; margin-bottom: 12pt; text-align: justify;"><span style="font-family: "Times New Roman","serif"; font-size: x-large;"> El Dr me mando dosis semanales muy bajitas, combinadas con antibioticos y ahora al escondido de el me tome una medicina para caballos (Zimectrin que ademas tiene prazicuantel) - creo que es la mejor medicina que existe.. no, no me creo llegua, apenas si soy una mula con aspiraciones!!!!!! Y me he mejorado muchisimo, estoy muy funcional digamos.. con sintomas de corazon y otros porque ademas tantos años de antibioticos al que no matan lo desbaratan como el matrimonio... pero ahi voy bien la mayoria de las veces. <br />
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</span></div><div class="MsoNormal" style="line-height: normal; margin-bottom: 12pt; text-align: justify;"><span style="font-family: "Times New Roman","serif"; font-size: x-large;">Y tengo un blog y como 600 amigos de Facebook con la misma enfermedad y les cuento sobre la Ivermectina y hay varios a quienes les he dado mi medicina y todos han mostrado recuperacion - una sra luego de 4 años en cama ya me escribio que fue a comprarle regalo al nieto y fue a mercar el otro dia y tambien fue a visitar a su hermana...<br />
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Entonces, respondo, no se si el Lyme Disease se cura o no... no lo se. En este momento aqui hay cientos de tratamientos muy costosos, inclusive han hecho los llamados "protocolos patentados" para tratar el Lyme pero nadie habla de curarlo solo de "remision"; muchos hacen tratamientos con medicinas herbales o maquinas que curan y miles de expertos opinan diariamente... y obvio que hay una gigantezca problematica politica y social detras de esta enfermedad, como la sifilis o el sida, pero esta no la quieren enfrentar o la quieren usar para enriquecer las farmaceuticas porque afecta a personas de todas las edades, no discrimina en sexo ni raza; causa cientos de sintomas que hacen las riqueza de muchos especialistas y es la enfermedad de siglo porque ya se rego por Europa y Africa... no se si esta en Sur America? <br />
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</span></div><div class="MsoNormal" style="line-height: normal; margin-bottom: 12pt; text-align: justify;"><span style="font-family: "Times New Roman","serif"; font-size: x-large;">Tal vez encuentren la cura una vez se convierta en pandemia y vendan su formula magica? O tal vez el Lyme Disease acabe con la humanidad? Suena como a una enfermedad de Nostradamus "pediran la muerte a gritos"? y tambien algunos dicen que este es el GU chino que mato a miles ... no se, la bolita de cristal no me funciona bien ultimamente para saber que va a pasar, se me daño el olfato perdiodistico con tanta infeccion y subjetividad? <br />
</span></div><div class="MsoNormal" style="line-height: normal; margin-bottom: 12pt; text-align: justify;"><span style="font-family: "Times New Roman","serif"; font-size: x-large;">... yo solo se que el presente es lo unico que tenemos y que todo bien!<br />
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Antes vivi en una velocidad ultrasonido, cinco minutos para escribir una nota antes que saliera al aire, ahora conoci el lado de los lentos que estorban en la fila... cerrando mi circulo!<br />
Hasta hoy en medio de todo, he aprendido mucho y Soy feliz!!!<br />
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Abrazos... no me imagine contar mi historia pero quiza le sirva a alguien... ojala!<br />
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Maria J.</span></div>MJhttp://www.blogger.com/profile/16614021020877246061noreply@blogger.com0tag:blogger.com,1999:blog-9207742591307790987.post-19330834733491947122011-08-02T04:29:00.000-07:002013-02-27T22:50:48.642-08:00LYME DISEASE: SURVIVING TO FLUKES AND PARAGONIMUS!<div class="MsoNormal">
<span style="font-size: large;">This is not good news but very needed to open the eyes and properly treat this Lyme, because Borrelia enters the immune system some big bad opportunistic bugs show up and if not treated well, there is no recovery at all... many Lymies have shown to have <u>FLUKES OR PARAGONIMUS</u>... sometimes Praziquantel could help (I found it in Zimectrin Gold for horses and there is a human version in the US); but unfortunately the only medicine that really seems to work for treating flukes is called TRICLABENDAZOLE, but the human version Fasinex is almost impossible to find anywhere in the world, so most countries have to treat with the veterinary version. If the person has flukes or paragonimus could get cancer if not properly treated and even after being treated; most lung problems are from the flukes, most liver problems are from these too and they also could cause intestinal parasitic infection. Please note these super mega bugs are not being treated with the antibiotics you have been taking, nor the IV abx, nor oral and less herbals; <b>if the person has flukes the medicine has to be as strong and equivalent as the bug.</b> </span><br />
<span style="background-color: #bf9000;"><b><span style="font-size: large;">This is not bacteria, nor filarial parasites, nor the common spaghetti worms some might have seen in their toilets, these are the masters of disguise, real huge monster demons! </span></b></span><br />
<span style="font-size: large;"> The way to test is in stool samples if the lab is looking for them, or if you see your "samples" like if you had eaten black beans... or with some brown seeds like whole almonds... plus the symptoms: Symptoms of parasite infection, specifically fascioliasis <span style="font-size: large;"><span style="font-family: "Arial","sans-serif";"><b>"</b></span></span>include headaches, rashes, muscle pain, jaundice, abdominal pain, loss of appetite, anemia, nausea, and vomiting". - And there might be other testing like DNA art testing or the biofeedback machines? those might save our lives I think if we get a proper dgx.</span></div>
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<span style="font-size: large;">This is other reading that states that the other anthelmintics could work but it is an older article, I present it here just for information: "Symptoms of schistosomiasis appear in three distinct phases. In the initial phase, symptoms include: fever, skin rash, abdominal pain, bronchitis, enlargement of the liver and spleen, and diarrhea. In the intermediate phase, symptoms include pathological changes in the intestinal and urinary tracts, and eggs in the urine and feces. The final phase results in complications involving major bodily systems."</span></div>
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<span style="font-size: large;">"Diagnosis is accomplished by finding eggs in the urine or feces. The most effective drugs for treating schistosomoiasis are organic trivalent antimonials. However, these drugs are toxic to humans, and of these drugs, only pentavalent stibogluconate is still in use.</span></div>
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<span style="font-size: large;">The current drug of choice is praziquantel. Other drugs used to treat schistosomiasis include metrifonate, oxamniquine, bithionol, albendazole, or mebendazole. The mechanism of these modern drugs is not known. However, it is known that one of the drugs (albendazole) starves the parasite and its offspring."... NOT TRUE, TRICLABENDAZOLE IS THE CHOICE NOW!</span></div>
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<span style="font-size: large;">If I may add, I found a veterinary medicine called TRIVENTOR that contains all the anthelmintics such as Triclabendazole, febendazole, Ivermectina and Praziquantel - does not contain Albendazole but I guess it is because the Albenda is the one that most probably hurt the Central Nervous system<span style="font-size: large;">, <span style="font-size: large;">but opposite of what we think, Albenda is one of the <span style="font-size: large;">antiparasitics </span></span></span>pref<span style="font-size: large;">f</span>ered by the <span style="font-size: large;">American</span> Doctors because they do not know the other anthelmintics plus they ignore the studies about the central nervous system...</span></div>
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<span style="font-size: large;">Anyways, I'm talking about monsters, huge, affecting Lyme patients who's bodies and immune system cannot combat by itself! Hope we all could get tested and treated against FLUKES!.</span><br />
<span style="font-size: large;">Read this: </span><br />
<span style="font-size: large;">"Symptoms of schistosomiasis are caused by the body's reaction to the eggs produced by worms, not by the worms themselves. </span><br />
<span style="font-size: large;"><span style="color: #000099;">Digestive symptoms</span>: The following list incomplete:<br />
abdominal pain, nausea, vomiting, inability to pass gas, abdominal pain on breathing, constipation, diarrhea, abdominal sensitivity, abdominal pain near navel, abdominal pain on sneezing, abdominal pain on activity, right-side abdominal pain, abdominal pain on coughing, abdominal swelling, upper abdominal discomfort, abdominal burning, abdominal bloating, malabsorption, partial intestinal blockage, Diverticulosis* Acute kidney failure ... nausea, vomiting, diarrhea * Bowel Obstruction ... green vomit, constipation, fecal vomiting, vomiting, abdominal swelling <b><a href="http://www.earthtym.net/ref-fluke-info.htm">http://www.earthtym.net/ref-fluke-info.htm"</a></b></span><br />
<span style="font-size: large;"><br /></span>
<b><span style="font-size: large;">The study made in Egip<span style="font-size: large;">t</span> that showed Triclabendazole as the proper medicine to treat for flukes here: </span></b><!--[if gte mso 9]><xml> <o:OfficeDocumentSettings> <o:AllowPNG/> </o:OfficeDocumentSettings> </xml><![endif]--><!--[if gte mso 9]><xml> <w:WordDocument> <w:View>Normal</w:View> <w:Zoom>0</w:Zoom> <w:TrackMoves/> <w:TrackFormatting/> <w:PunctuationKerning/> <w:ValidateAgainstSchemas/> <w:SaveIfXMLInvalid>false</w:SaveIfXMLInvalid> <w:IgnoreMixedContent>false</w:IgnoreMixedContent> <w:AlwaysShowPlaceholderText>false</w:AlwaysShowPlaceholderText> <w:DoNotPromoteQF/> <w:LidThemeOther>EN-US</w:LidThemeOther> <w:LidThemeAsian>X-NONE</w:LidThemeAsian> <w:LidThemeComplexScript>X-NONE</w:LidThemeComplexScript> <w:Compatibility> <w:BreakWrappedTables/> <w:SnapToGridInCell/> <w:WrapTextWithPunct/> <w:UseAsianBreakRules/> <w:DontGrowAutofit/> <w:SplitPgBreakAndParaMark/> <w:EnableOpenTypeKerning/> <w:DontFlipMirrorIndents/> <w:OverrideTableStyleHps/> </w:Compatibility> <m:mathPr> <m:mathFont m:val="Cambria Math"/> <m:brkBin m:val="before"/> <m:brkBinSub m:val="--"/> <m:smallFrac m:val="off"/> <m:dispDef/> <m:lMargin m:val="0"/> <m:rMargin m:val="0"/> <m:defJc m:val="centerGroup"/> <m:wrapIndent m:val="1440"/> <m:intLim m:val="subSup"/> <m:naryLim m:val="undOvr"/> </m:mathPr></w:WordDocument> </xml><![endif]--><!--[if gte mso 9]><xml> <w:LatentStyles DefLockedState="false" DefUnhideWhenUsed="true"
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<b><span style="font-size: large;"><a href="http://www.emro.who.int/publications/emhj/0402/07.htm">http://www.emro.who.int/publications/emhj/0402/07.htm</a></span></b></div>
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<span style="font-size: large;">Links of pictures of parasites a wonderful blog, by </span></div>
<pre><span style="font-size: large;"><b>Carol Poore</b>, thank you:</span></pre>
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<span style="font-family: "Times New Roman","serif"; font-size: large; line-height: 115%; mso-fareast-font-family: "Times New Roman";"><a href="http://www.epi-center.com/parasite.html">http://www.epi-center.com/parasite.html</a></span></div>
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<b><span style="font-size: large;">And more Links and info about triclabendazole, </span></b></div>
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<span style="font-family: "Times New Roman","serif"; font-size: large; line-height: 115%;"><a href="http://www.drugs.com/mmx/triclabendazole.html">http://www.drugs.com/mmx/triclabendazole.html</a></span></div>
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<span style="font-family: "Times New Roman","serif"; font-size: large; line-height: 115%;"><a href="http://parasitology.com/worms/index.html">http://parasitology.com/worms/index.html</a></span></div>
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<span style="font-family: "Times New Roman","serif"; font-size: large; line-height: 115%;">"[Fascioliasis (treatment)]<a href="http://www.drugs.com/mmx/triclabendazole.html#F0036239996"><sup><span style="color: blue;">1</span></sup></a>—<b style="mso-bidi-font-weight: normal;">Triclabendazole is used as a primary agent in the treatment of fascioliasis caused by <i>Fasciola hepatica</i> (sheep liver fluke) and <i>Fasciola gigantica</i> (giant liver fluke). <a href="http://www.drugs.com/mmx/triclabendazole.html#citec00362301"><sup><span style="color: blue;">{01}</span></sup></a> <a href="http://www.drugs.com/mmx/triclabendazole.html#citec00362302"><sup><span style="color: blue;">{02}</span></sup></a> <a href="http://www.drugs.com/mmx/triclabendazole.html#citec00362307"><sup><span style="color: blue;">{07}</span></sup></a> <a href="http://www.drugs.com/mmx/triclabendazole.html#citec00362308"><sup><span style="color: blue;">{08}</span></sup></a> <a href="http://www.drugs.com/mmx/triclabendazole.html#citec00362311"><sup><span style="color: blue;">{11}</span></sup></a> <a href="http://www.drugs.com/mmx/triclabendazole.html#citec00362313"><sup><span style="color: blue;">{13}</span></sup></a><br />
</b><br />
<b style="mso-bidi-font-weight: normal;">[Paragonimiasis (treatment)]<a href="http://www.drugs.com/mmx/triclabendazole.html#F0036239996"><sup><span style="color: blue;">1</span></sup></a>—Triclabendazole is used as an alternative agent in the treatment of paragonimiasis caused by <i>Paragonimus westermani</i> (lung fluke) <a href="http://www.drugs.com/mmx/triclabendazole.html#citec00362301"><sup><span style="color: blue;">{01}"</span></sup></a></b></span><br />
<span style="font-size: large;"><b><span style="font-family: "Times New Roman","serif"; line-height: 115%;">Mechanism of action/Effect:</span></b><span style="font-family: "Times New Roman","serif"; line-height: 115%;"><br />
<br />
Fasciolicidal not only against the adult worms present in the biliary ducts, but also against the immature larval stages of <i>Fasciola</i> migrating through the hepatic parenchyma; the mechanism of action is not thoroughly understood; however, triclabendazole is shown to penetrate into liver flukes by transtegumentary absorption followed by inhibition of the parasite's motility, probably related to the destruction of the microtubular structure, resulting in the death of the parasite; the immobilizing effect is paralleled by changes in the parasite's resting tegumental membrane potential, strongly inhibiting the release of proteolytic enzymes, a process that appears critical to the survival of the parasite <a href="http://www.drugs.com/mmx/triclabendazole.html#citec00362305"><sup><span style="color: blue;">{05}</span></sup></a> <a href="http://www.drugs.com/mmx/triclabendazole.html#citec00362306"><sup><span style="color: blue;">{06}</span></sup></a> <a href="http://www.drugs.com/mmx/triclabendazole.html#citec00362307"><sup><span style="color: blue;">{07}</span></sup></a>.</span></span><br />
<span style="font-size: large;"><span style="font-family: "Times New Roman","serif"; line-height: 115%;"> <b>Absorption:</b><br />
Following oral administration, triclabendazole is absorbed from the gastrointestinal tract; absorption is increased twofold to threefold when triclabendazole is taken after a fatty meal <a href="http://www.drugs.com/mmx/triclabendazole.html#citec00362302"><sup><span style="color: blue;">{02}</span></sup></a> <a href="http://www.drugs.com/mmx/triclabendazole.html#citec00362308"><sup><span style="color: blue;">{08}</span></sup></a>.
<b>Distribution:</b><br />
Triclabendazole and its metabolites attain high concentrations in the biliary tract, through which they are excreted back into the intestine over a period of several days <a href="http://www.drugs.com/mmx/triclabendazole.html#citec00362302"><sup><span style="color: blue;">{02}</span></sup></a>; less than 1% of orally administered triclabendazole is distributed into breast milk <a href="http://www.drugs.com/mmx/triclabendazole.html#citec00362309"><sup><span style="color: blue;">{09}</span></sup></a>.
<b>Biotransformation:</b><br />
Triclabendazole is oxidized to sulfoxide (the primary metabolite) and sulfone (present in lesser amounts) over the first 24 hours following oral administration <a href="http://www.drugs.com/mmx/triclabendazole.html#citec00362302"><sup><span style="color: blue;">{02}</span></sup></a>.</span></span><br />
<span style="font-size: large;"><span style="font-family: "Times New Roman","serif"; line-height: 115%;"> <b>Time to peak concentration:</b><br />
Approximately 8 hours <a href="http://www.drugs.com/mmx/triclabendazole.html#citec00362302"><sup><span style="color: blue;">{02}</span></sup></a>.</span></span><br />
<span style="font-size: large;"><span style="font-family: "Times New Roman","serif"; line-height: 115%;"> <b>Elimination:</b><br />
Fecal—Approximately 95% of orally administered triclabendazole (unchanged or as the primary metabolite) is excreted in the feces <a href="http://www.drugs.com/mmx/triclabendazole.html#citec00362309"><sup><span style="color: blue;">{09}</span></sup></a>.<span style="font-size: large;"><b> </b></span> Renal—Approximately 2% is excreted in the urine <a href="http://www.drugs.com/mmx/triclabendazole.html#citec00362309"><sup><span style="color: blue;">{09}</span></sup></a>.
<b>Precautions to Consider</b><br />
<a href="http://www.blogger.com/post-edit.g?blogID=9207742591307790987&postID=1933083473349194712&from=pencil" name="s00362331"></a>
<b>Mutagenicity<span style="font-size: large;"> </span></b>Studies conducted in laboratory animals have not shown triclabendazole to be mutagenic <a href="http://www.drugs.com/mmx/triclabendazole.html#citec00362307"><sup><span style="color: blue;">{07}</span></sup></a> <a href="http://www.drugs.com/mmx/triclabendazole.html#citec00362308"><sup><span style="color: blue;">{08}</span></sup></a>"</span></span><br />
<br />
<span style="font-family: "Times New Roman","serif"; font-size: large; line-height: 115%;">BUT THE ONLY POSSIBLE TRICLABENDAZOLE IS VETERINARY THE HUMAN VERSION IS STILL IN LIMBO LAND! FASINEX IS IMPOSIBLE TO BUY, SO NADA, THERE IS NON <span style="font-size: large;">HUMAN MED TO TREAT FOR FLUKES, </span><span style="font-family: "Arial","sans-serif";"><b><span style="font-size: large;">NO EXISTE!</span></b></span></span><br />
<span style="font-family: "Times New Roman","serif"; font-size: large; line-height: 115%;"><span style="font-family: "Arial","sans-serif";"><b><span style="font-size: large;">Only vet med and it is considered <span style="font-size: large;">illegal in the US? ... :(</span></span></b></span></span><br />
<span style="font-family: "Times New Roman","serif"; font-size: large; line-height: 115%;"><b><sup><span style="color: blue;"> </span></sup> </b></span><br />
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<span style="font-size: small;"><b>NOTE: LYME THE ROLLERCOASTER BLOG DOES NOT OFFER, DOESN'T GIVE, NOR INTENDS TO GIVE ANY MEDICAL ADVISE NOR MEDICAL RECOMMENDATIONS.</b><b><span style="font-family: "Arial","sans-serif";"> Just sharing my thoughts, research and experience!</span></b></span><br />
<span style="font-size: small;"><b><span style="font-size: large;"><span style="font-family: "Arial","sans-serif";"><span style="font-size: large;"> </span></span></span></b></span></div>
MJhttp://www.blogger.com/profile/16614021020877246061noreply@blogger.com0tag:blogger.com,1999:blog-9207742591307790987.post-43331818605808493532011-07-28T16:51:00.000-07:002011-08-11T05:41:51.552-07:00Why we need to use Ivermectin or other antiparasitics for treating lyme Disease?<div class="MsoNormal"></div>My friend Thane Fredrickson-Lyme asked me:<br />
"Hey Maria, can you briefly tell me your theory of why we need to use Ivermectin or other antiparasitics for treating lyme?"<br />
Here is my answer, I'm doing a document so it can help others.<br />
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<div class="MsoNormal">Thank you for saying MY THEORY, because I don't have the scientific way to prove it, I'm just a lymie! Most of what I say is learned from my Dr in Colombia who I call and has taught me and helped me through this nightmare - ten Drs here in Fl dismissed me and I was dgx and tested in Maryland with Lyme Borreliosis, Babesia, and two more bugs in my blood by Dr J.</div><div class="MsoNormal"><br />
</div><div class="MsoNormal">I have written a couple of blogs showing that Lyme Disease is basically a parasitic infection, not a bacterial alone.For me the bacteria in Lyme comes after the parasitic infection.</div><div class="MsoNormal">If it is parasitic needs anthelmintics and my doc thinks the treatment should not be antimalarials because those act by immune suppression so they are not helpful when talking about multiple infections, like killing the cat leaving the rats take over?</div><div class="MsoNormal"><br />
</div><div class="MsoNormal">So why is Lyme parasitic? </div><div class="MsoNormal">1. It is a <b>zoonotic infection</b> - read CDC, all zoonotic</div><div class="MsoNormal">infections are parasitic; so why we hear lyme is bacterial and the parasitic side was erased? zoonotic=parasitic = all but Lyme? weird!</div><div class="MsoNormal">2. <b> </b><b>Borrelia</b> goes intracellular - if this doesn't mean parasitic what it means? and Borrelia doesn't die with abx, lol, of course if it is a parasite behavior it needs the medicine for it!</div><div class="MsoNormal">3. Dr Burgdorferi talked about <b>filarial infection</b> and other of the infections transmitted by the tick simultaneously with the Borrelia, but that was ignored? US didn't want to hear there is a parasitic infection passed by the tick? why? because it is like a malaria?</div><div class="MsoNormal"><div class="MsoNormal">filarial like as the worse parasitic infection in Africa? Well Dr Sapi after so many studies decided to not ignore those words and recently stated that if there is a filarial infection in Lyme as Dr Burgdorferi said, this could be the reason why some patients never recover with conventional treatments and would requires "strong antifilarial treatments. The drug of choice in Europe is Ivermectin" - her words almost literal. She said she suspect a filarial infection similar to the onchoneriasis or River blindness of Africa but not the same one - we don't get elephantiasis, but yes we can have bugs coming out the eyes, and in the brain and out from the skin.</div><div class="MsoNormal"> <a href="http://en.wikipedia.org/wiki/Filariasis">http://en.wikipedia.org/wiki/Filariasis</a></div><div class="MsoNormal">"Can species other than bacteria, virus or fungus be responsible for these chronic problems found in Lyme patients? It has been proposed that certain parasites could also be a factor in Lyme disease. European doctors have already incorporated Ivermectin, an antihelminth drug, into their Lyme disease protocol with surprising success. Ivermectin is well known for its effectiveness against filarial nematode infections and is often used by veterinarians to eradicate parasitic infections ... Can Lyme disease patients have filarial nematode co-infection and can they acquire this infection from ticks? The only evidence reported of filarial worm presence in ticks was from a study by Burgdorferi’ in 1984 where thirty microfilarial worms (species not identified) were found in one adult Ixodis dammini tick in Shelter Island, NY. <sup>(4) </sup>Black flies have already been identified as vectors of filarial nematodes. <sup> </sup>Interestingly, ticks can also be used as an <em>in vitro</em> experimental vector system to study the transmission of filarial nematodes and it was shown that the infected nymphal stage could transmit the filarial worms. <sup> </sup>If filarial nematodes could be a tick-borne co-infection of Lyme disease patients, their eradication would require additional treatments using specific filaricidal drugs, which could explain why standard antibiotic based protocols often fail in some chronic Lyme disease cases."</div><div class="MsoNormal"><br />
</div><div class="MsoNormal"><sup> </sup> </div></div><div class="MsoNormal">4. <b>Babesia</b> is not enough to consider? LD patients with Babesia are given antibiotics to treat them, like if the Babesia could be treated with antibiotics? it is like trying to kill a snake with flea spray? yes the spay has killed tons of fleas but the snake is not going to die until you pour this flea sprays for years and tons of it right? Babesia is a malaria kind of parasite and malaria is been treated with Ivermectin in South America and Africa with outstanding results for about 20 years? So if the Drs here didn't give me any treatment for Babesia I had to dare to try to help my self and the human Ivermectin I took initially showed me I could recover, so I kept treating my self with a low dose, once a week and because of the recovery I have had much different and significance compared to when I was treated with antibiotics alone, I start posting about Ivermectin as a vital part to help and treat Lyme Disease patients. And I didn't know about the filarial infection yet; now more than ever I am convinced that the first drug of choice has to be Ivermectin.</div><div class="MsoNormal">Tons of research in Norway and even here in the US have shown Lyme Disease cannot be treated with antibiotics alone, and the studies that have been made with potent herbs like Samento, banderol, Cat's claw always end up using an anthelmintic to kill the remaining parasites.</div><div class="MsoNormal">5. <b>Flukes:</b> as my Dr states lots of opportunistic show up when there are huge poly-infections but what if flukes are the ones causing the majority of the damage? I have seen that most of my Lymie friends end up having Flukes or in the lungs, or the liver or the intestines... these huge parasites cannot be ignored at all. I have been taking Praziquantel combined with Ivermectin and felt the best in 6 years of nightmare. The medicine I got is called Zimectrin Gold and it is veterinary. I also got a horse medicine called Triclabendazole, very difficult to find in the world, to treat the flukes in case the Praziquantel is not enough; if flukes are not treated people get cancer... or people with cancer have them...</div><div class="MsoNormal">6. <b>Parasites in the intestines</b>, with Lyme for sure, the opportunistic are there and with a compromised immune system they are reproducing every full moon and require to be treated. Yes Ivermectin is good for this! But note, when I talk about parasites in Lyme these are the least ones I'm talking about, the chain is much bigger than just having parasites in the intestines; these are just the obvious result or product from such multiple infection.</div><div class="MsoNormal"><br />
</div><div class="MsoNormal">And there is so much more research that shows Lyme Disease is by all means a multi-infection of parasites and bacteria that has to be properly treated: first the big ones then the small ones. It is the logic way to do it. My Dr said, you kill the master and the others in the chain or go with him or will be easier to defeat with other medicines or even your own immune system could fight them. The Drs in the US chose the other way around, first antibiotics and even IV antibiotics for three years and then some might give Flagyl, or other use antimalarials like Mepron or Malarone or Artemisinin... an approach that has shown no complete recovery and barely a so called remission in some patients.</div><div class="MsoNormal"><br />
</div><div class="MsoNormal">I'm talking recovery as being healthy, strong and able to live a normal life. My heart is hurt and my liver and stomach too after so many years of antibiotics, full of fungus and other toxins but I can tell you my muscles are coming back after the Ivermectin treatments, like if I am going to a gym or having any kind of workout which not only I have not had nor any kind of food or shakes for this, but I am almost 50 years old, sick sedentary 6 years and this never seem to be even possible after all my muscles fall off from my bones in 2006 when Lyme started... I believe there could be recovery from LD with Ivermectin and proper antiparasitic treatment! Note: if you are lucky enough to have a good Chinese Doctor to treat you for your GU symptoms you won’t need my advice or Ivermectin!</div><div class="MsoNormal"><br />
</div><div class="MsoNormal">Hope my info helps. Will post it and do another blog hoping I can reach Lymies and they can recover slowly as I have had this God given gift too!</div><div class="MsoNormal"><br />
</div><div class="MsoNormal">Hugs </div><div class="MsoNormal"><br />
</div><div class="MsoNormal">Maria.</div>MJhttp://www.blogger.com/profile/16614021020877246061noreply@blogger.com0tag:blogger.com,1999:blog-9207742591307790987.post-31121035692546047282011-05-31T01:54:00.000-07:002013-02-27T22:51:52.247-08:00LYME DISEASE: AN OVERLOAD OF BUGS AND SYMPTOMS!<!--[if gte mso 9]><xml> <o:OfficeDocumentSettings> <o:AllowPNG/> </o:OfficeDocumentSettings> </xml><![endif]--><!--[if gte mso 9]><xml> <w:WordDocument> <w:View>Normal</w:View> <w:Zoom>0</w:Zoom> <w:TrackMoves/> <w:TrackFormatting/> <w:PunctuationKerning/> <w:ValidateAgainstSchemas/> <w:SaveIfXMLInvalid>false</w:SaveIfXMLInvalid> <w:IgnoreMixedContent>false</w:IgnoreMixedContent> <w:AlwaysShowPlaceholderText>false</w:AlwaysShowPlaceholderText> <w:DoNotPromoteQF/> <w:LidThemeOther>EN-US</w:LidThemeOther> <w:LidThemeAsian>X-NONE</w:LidThemeAsian> <w:LidThemeComplexScript>X-NONE</w:LidThemeComplexScript> <w:Compatibility> <w:BreakWrappedTables/> <w:SnapToGridInCell/> <w:WrapTextWithPunct/> <w:UseAsianBreakRules/> <w:DontGrowAutofit/> <w:SplitPgBreakAndParaMark/> <w:EnableOpenTypeKerning/> <w:DontFlipMirrorIndents/> <w:OverrideTableStyleHps/> </w:Compatibility> <m:mathPr> <m:mathFont m:val="Cambria Math"/> <m:brkBin m:val="before"/> <m:brkBinSub m:val="--"/> <m:smallFrac m:val="off"/> <m:dispDef/> <m:lMargin m:val="0"/> <m:rMargin m:val="0"/> <m:defJc m:val="centerGroup"/> <m:wrapIndent m:val="1440"/> <m:intLim m:val="subSup"/> <m:naryLim m:val="undOvr"/> </m:mathPr></w:WordDocument> </xml><![endif]--><!--[if gte mso 9]><xml> <w:LatentStyles DefLockedState="false" DefUnhideWhenUsed="true"
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©</div>
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This is my thinking, not a scientific advice of course:</div>
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I was asked by a friend if I agree we all have a germ overload, and if I think that by killing the parasites the bacteria and other might be fixed by the immune system?</div>
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Yes in Lyme Disease there is an overload of bugs, organisms, bacteria, protozoans, viruses and mold. </div>
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Why or how? By the transmission of the tick bite, other might be awakened because the immune system is suppressed maybe by some bacteria capable of doing this or precisely because the system is totally overloaded. Also because the ticks transmit not just one type of bugs, at least the American ticks seem to pass more than one organism and they all enter our bodies and create an "ecosystem" inside us.</div>
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For example the mold, we might all have some of it in our "regular healthy lives", but because of the infection, the parasitic die off or the large amounts of antibiotics the mold grows. So probably it was not received from the tick but it is an "opportunistic organism"?? When we kill the parasites if there are no bacteria to eat that dead body, the body will have a fermentation process which really means fungi or mold trying to destroy it. Meaning count on having mold too for sure, and this is a big organism not easy to eradicate!</div>
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Another thing very obvious to me is, if we have a little stick inside our skin, let's say the tip of a finger and we do not take it out what happens? it gets infected, meaning the bacteria would show up and live there unless we treat the infection and get rid of the stick. Now imagine thousands of sticks inside our bodies, and then hundreds of thousands in the blood, brain, muscles? well, those are the parasites and yes the bacteria feeds from the left overs of these parasites. There are some researchers who dare to say that these parasites are so smart they "grow" these bacteria as food for them?</div>
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I just think it is obvious to have multiple organisms if an infection is not treated on time, more this type of zoonotic Disease that brings big parasites that go to our blood and then the brain and glands and muscles and bones. So of course the response is to have an overactive immune system, adrenal system, circulatory system; the Central nervous system is infected almost since the beginning, the Lymphatic system is their favorite dessert and with all these the constellation of symptoms is obvious. Pains of all types, infection all over, septicemia, countless signs.</div>
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So because of my posts you ask me if I think that by first treating the parasites the other infections could be fixed by the immune system? I would have to say I don't know for sure, but I can say that it is not logic to treat the bacteria first and after years of being devoured by parasites consider treating them. I can say for sure the logic is to treat the big ones first. Yes treat the parasites and then try to fix the infections and mold and viruses before the body is so broke, is the logic thread. I cannot understand people having intravenous antibiotics for two three years and not having one anti-parasitic. It is like trying to kill a snake with flea spray? yes it has killed thousands of fleas but it might take many years to kill that snake!</div>
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But the problem is much bigger; the problem is the concept of what Lyme Disease is or what it is not. I hear people saying, "my Doctor found my bigger problem was not Lyme but the Babesia?"; others "I found pots is my problem and not LD"? So the concept of what is Lyme has to be defined, to be able to properly treated; the same as the bugs in Lyme have to be IDENTIFYIED to be properly treated!</div>
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I've seen LD as the multi-infection that generates a constellation of symptoms, but I don't loose the North of seeing the origin of such infection as a zoonotic disease and as such what type of medicines to use. This because most Drs and specialists treat the symptoms but not the cause, so the person receives tons of pain killers, psych medicines and hundreds of supplements but not even one anthelmintic? So Lyme is what and how it must be addressed to fully recover the person? </div>
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So we have to go back to the concept again because most Doctors and medical books in the US think there are no parasites in this huge piece of earth; everything is free of worms and longer bugs? the soil, the water, the grass, the animals?? I don't know why parasites are denied with such fervor, lol, it is like saying the rest of the world could be round but this part is flat! </div>
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So if the WISE say there are no parasites at all, just very weird cases, so exceptional they are good to do a scary TV program full of Monsters, how can someone like me say LD has a huge component of parasitic infection? And let me clear, not just me but a Dr and a group of Drs that have influence from other places of the world, meaning this is not "American made"... so is there or is there not a parasitic infection in Lyme Disease. Are parasites transmitted by the tick when it bites the victim or not? Is Babesia a parasite? Is Borrelia a parasite? and do some of the co-infections re or not parasites or act like parasites? And if this concept is not defined due to it might raise susceptibilities as saying the US is now ewww full of parasites, LD is not going to be properly treated. Like the spray for fleas to try to kill a snake, or ten snakes or one hundred snakes or thousands hatched every 21 days inside our bodies... does this is a picture that needs to be taken care or we can still ignore it to not be offended?</div>
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How come LD is "malaria like"? i don't understand what is to be like and not to be it, what this means medically or scientifically talking; I just understand the words that mean it is as bad as malaria and it should be treated with the same priority as this disease, is this correct? How come "Babesia" is a parasite that acts like the parasite of the falciparum malaria but it is not treated as a bad dangerous parasite? Amoxicillin for these? Doxycycline for two weeks? This treatment was not even made in the past century in the endemic areas of the planet why would that be the treatment in the US in this century? I asked the Dr if he would consider the blood transfusion and he laughed at me... why? Don’t I deserve to be properly treated for such infection? My friend C asked her Doctor to test her and consider treating her for parasites, her Doctor said he won't test her because he won't change the protocol no matter the results of the labs! TRUE STORY! And many like this one that has name and last name! </div>
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So again, are there or are there not parasites in LD and if the answers is yes should they be treated or not??? Is it ok and proper to not treat parasites and not to treat the zoonotic parasitic infection in Lyme Disease?</div>
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And if this brings some light at the end then there will be the discussion of what is a parasite and what not? Because many think parasites are just intestinal, they just get the concept of a white long worm, but can you even think what is like to have bugs that go inside the red blood cell and feed out from it, live there, multiply inside there; or inside the brain cells? Something not so serious to treat or something too ewww to talk about? We have parasites coming out of our eyes, we've seen them and have pictures. Bugs coming out from our skin, bugs killing our brain cells to the point the "DEPRESSION" is nothing different than brain damage made by the parasites that leave the cell blank so we cannot think, remember things, connect images, get to the extreme point of not even being able to pray, the brain just can't do it, too hard to do it. Does this sounds strange? it is not for any Lymie! </div>
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So are parasites just white long worms or those "malaria like" as Babesia, that invade our red blood cells three bugs at a time, sucking our life out, are, or not parasites, and should they be treated or not?</div>
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And of course we do have intestinal parasites, lol, those are the easiest ones to treat, those are the less of our problems; so why not treat them? Why the medical profession in the US does not deworm regularly and moreover why not deworm and detox a person who is infected in so many ways with so many organisms? </div>
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So, do I think that by treating the parasites the other bugs might be fixed by our own bodies? Still cannot say the last word, hope there is someone that could, but Dr K said that while treating the bigger bugs the smaller can be detoxed too; and this Dr in Fl said that Borrelia attaches to the parasites so we cannot let one parasite in the body not treated in order to cure Lyme Disease.. if this answers part of the question?</div>
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The other problem I see is that if all the bugs were properly identified and addressed the point would be how to treat them, in which order and when? From the biggest to the smallest, and then repeat treatments, ok that sounds logic, but how to know the exact combination? The more you research about Lyme the more weird names show up, so can you explain me how can the tick in North America transmit Rickettsia, Mycoplasma, Bartonella, Babesia, Borrelia, Viruses, etc??? Does each Lymie has them all? Or just some of those? And to put the cherry on top of this dessert, the homeopathic Doctors insist there is a huge load of metals blocking the body that have to be treated too to be able to respond to the rest of the long treatment! </div>
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So we are talking about a multi-bacterial, poly-parasitic infection with numerous co-infections that cause a constellation of symptoms and damage to the body and health that is not clear how to detect it, to address it; it is denied, hidden and ignored, that is now the plague of the century, spread from the US to the world and no one knows how to cure it? (I say use anthelmintics to start, Eureka!!!).</div>
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I don't know if the chicken was first than the egg but one thing is certain, a zoonotic infection is parasitic everywhere of the planet; an "intracellular bacteria - like Borrelia - means it is a parasite but smaller - and if Babesia is not treated the person would never recover. So talking parasites is talking Lyme Disease.</div>
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The one only truly good thing I find after so much suffering this disease brings is that no matter how many say this is chronic and won't be cured, when properly addressed by killing the parasites and treating the infections, in most cases, even the very lost ones, the immune system responds and recovers and the person can become healthy after being sick long time. I have seen that with people just receiving some antibiotics and feeling some recovery and others having anthelmintic and starting to live again. Even the anemia goes away by itself! The immune system doesn't seem to be broken, it is overloaded and affected, but it still works everyday truly hard to help us out; it is not chronic by any means. Treat the infection and the chronic is gone! </div>
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So my answers is yes, I do think that if you treat first the parasites and re-treat from time to time, and properly address the infections and co-infections the immune system would do a better job and the healthy life would come back, slowly but would do! </div>
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No it is not a fake expectation; it is the reality some business people want to take away from us just to make money by treating forever or by some companies that do not want to do long term treatments, but the sun is there no matter how much they try to hide it with a finger!</div>
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M.J.<br />
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<span style="font-size: large;"><b><span style="font-size: x-small;">NOTE: LYME THE ROLLERCOASTER BLOG DOES NOT OFFER, DOESN'T GIVE<span style="font-size: x-small;">, </span> NOR INTENDS TO GIVE ANY MEDICAL ADVISE NOR MEDICAL RECOMMENDATIONS.</span></b></span><span style="font-size: small;"><b> <span style="font-family: "Times New Roman","serif"; font-size: x-small;">THESE ARE JUST MY THOUGHTS, IDEAS, RESEARCH AND EXPERIENCE SHARED.</span></b><span style="font-size: x-small;"></span></span></div>
MJhttp://www.blogger.com/profile/16614021020877246061noreply@blogger.com0tag:blogger.com,1999:blog-9207742591307790987.post-82038867584699365602011-05-16T04:25:00.000-07:002013-02-27T22:52:41.660-08:00LYME DISEASE, IS AN INFECTION BASED IN THE MEDULLA OBLONGATA!<div class="MsoNormal">
<span style="font-size: large;">"The <b>medulla Oblongata</b> is the lower half of the <a href="http://en.wikipedia.org/wiki/Brainstem" title="Brainstem">brainstem</a>. In discussions of neurology and similar contexts where no ambiguity will result, it is often referred to as simply <b>the medulla</b>. <b>The medulla contains the cardiac, <a href="http://en.wikipedia.org/wiki/Respiratory_center" title="Respiratory center">respiratory</a>, <a href="http://en.wikipedia.org/wiki/Area_postrema" title="Area postrema">vomiting</a> and <a href="http://en.wikipedia.org/wiki/Vasomotor" title="Vasomotor">vasomotor</a> centers and deals with <a href="http://en.wikipedia.org/wiki/Autonomic_nervous_system" title="Autonomic nervous system">autonomic</a>, involuntary functions, such as breathing, heart rate and blood pressure</b>." - From my friend Wikipedia!</span></div>
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<span style="font-size: large;">Reading Sarah Vaughter's blog she said LD infection starts in the "Medulla Oblongata", YES!!!! I have been saying the infection is based behind the nose, that is is like a sinus but stronger, but this information of the medulla fits perfectly: "The medulla contains the cardiac, respiratory, vomiting and vasomotor centers and deals with autonomic, involuntary functions, such as breathing, heart rate and blood pressure." So it is affecting our bodies before even spreading anywhere else! </span><span style="background-color: #38761d; font-size: large;"> </span></div>
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<span style="font-size: large;">This is why the heart rate is affected, not because of the thyroid this one comes later; this is why the breathing stops and changes during the day or while sleeping; this is why we can get involuntary movements and look like drunk people or crazy ones; from the medulla the infection travels to the "nerves" or to anywhere of our Central Nervous system and that is the cause of such horrible pains. The infection in the medulla is why we vomit and have diaharreahs; this is why we loose our memory, become forgetful, blurry vision, neurological disorders, anger, depression! </span></div>
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<b><span style="font-size: large;">This nice blog of "Sacredluna" teaches to "use the brain" to contact "Our Higher Source" of the Universe by "putting images in the medulla", they say: </span><span style="font-size: large;">"There is a non-physical cord that attaches us through our Medulla Oblongata to our origin", well, from experience I can say that when the medulla is infected with Lyme Disease there is no contact with God, nor with happiness, cannot laugh, cannot even love! Maybe that website is saying the biggest truth, if the medulla is infected there is no connection to the Universe and that is why there is clinical depression and suicidal fears?</span></b></div>
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<span style="font-size: large;">The important thing is to know where it starts to be able to end it. Learning that the bugs are grounded in the medulla gives the option of treating it directly. Just wonder if the big wise medical organizations of the country and the world are going to maintain their guidelines to treat Lyme Disease with just two weeks of antibiotics to an infection that is parasitic and that is located in the base of the brain spreading over all the brain and the body? </span></div>
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<span style="font-size: large;">The first symptoms and all the relapses fit perfectly, it is not a sinus but rather an infection in the medulla and from there it goes to the rest of the brain, the sinuses, mouth, glands, thyroid, heart, wowowowowowwww! </span></div>
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<b><span style="font-family: "Times New Roman","serif"; font-size: large;"><span style="background-color: #6aa84f; font-family: Times,"Times New Roman",serif;"><span style="background-color: #274e13;">I'm I discovering the hot water here? everyone knew this but me? I'm in shock! This is why the heart rate is affected, not because of the thyroid; this is why the breathing stops and changes; this is why we can get involuntary movements; from the medulla the infection travels to the "nerves" or to anywhere of our Central Nervous system; come one this is the place where all Lyme Disease starts and where it has to be ended!</span><span style="background-color: #b6d7a8;"> </span>Attack the base!!!</span></span></b> </div>
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<span style="font-size: large;"> When the tick bites transmits infection from his mouth to the skin and from there this infection moves to the blood stream the same as it does with the mosquito bite transmitting malaria. The infection is not just bacterial as all say trying to dismiss the severity of Lyme Disease; the infection are parasites who look for food and for a place to make their camping! When they invade the blood the anemia is severe; the malaria parasites go inside the red blood cells, one bug per one red blood cell; while the Lyme parasites are three at a time invading each red blood cells, three times worse than malaria - this is the Babesiosis - and the Borrelia that is always called a "resistant bacteria" it is just another "intracellular bacteria" which certainly means another type of parasite malaria like. So after having such infection in the organism the body breaks. The sudden anemia causes fatigue and from there tons of symptoms start. The bugs stay in the blood for a short period of time but soon they migrate to other places, they want to hide in the smaller veins to hide from the attacks of the immune system and or antibiotics when the person receives treatment, and they're hungry too, so they go where they can feed and reproduce better. The malaria parasites go to the liver and the brain, that's why they kill their host so fast. The bugs of LD are smarter, they migrate to many places to not kill their host, there are many cases of people living with Lyme for more than 20 or 30 years and all the time symptomatic and suffering; yes many others die from a heart attack and other complications but these bugs do not pretend to kill just to live long. </span><br />
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<span style="font-size: large;">The parasites of Lyme Disease love to feed out of brain cells, of glands tissues, organ tissues, bones and muscles, and of course their favorites are all related to the brain like nerves all over the body. Lyme Disease in inflammatory - of course the body swells trying to get rid of these multiple infections; LD is autoimmune well, sort of because if the red blood cells are attacked by some bugs, also the Borrelia bugs hiding inside the white blood cells make the infection look like the body attacking it self right? Lyme Disease is "chronic" well, it lasts until the bugs are killed and certainly two weeks of Doxy do not do the miracle.Lyme is the best imitator because it looks like ALS, MS, Lupus, etc, well it is not imitating it is doing it; the bugs are infecting the muscles so the fibromialgia is not fake it is real; the bugs are eating the brain so the neurological is not a fake Parkinsosn or Alzheimers it is real damage until the bugs are killed or wiped out; it is not imitating heart problems it is a real infection in the heart; it is not a fake arthritis it is more real than the old known one because the bugs are feeding of the tissue around the bones; but if you ask me how to combat these multiple symptoms so complex and painful I would easily say killing the bugs, but not, that is not made, barely. The wise ones wrote that two weeks of Doxycicline could clean the infection if catch "on time" or four weeks of intravenous antibiotic if not treated early would wipe off all the bugs, so inf the person is still sick they say the illness is chronic and won't treat anymore. Meaning will let the bugs to reproduce now freely everywhere and anywhere they want, owners of that host. But please notice, Doctors will give tons of opiates for the pain, lots of psychiatric medicines for the neurological symptoms, many drugs to help the sleeping disorders and thousands of supplements to help the body heal; their hands do not shake to prescribe morphine, hydrocodone, and all those strong pain killers; but try to convince them to give you Flagyl for two weeks or Albendazole, or Ivermectin for one month? noo, those drugs are too strong and can cause reactions. The IV antibiotics are too risky, the long antibiotics treatments are not good, and so on until finding that the only ones that would treat longer, but still denying parasites, are the ones that charge more... </span></div>
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<span style="font-size: large;">Lyme Disease is an infection originated from the base of the brain, it has to be treated there to be eradicated, cannot be left untreated infecting the brain and the rest of the Central Nervous system and the Lymphatic system and the circulatory system and the muscles and organs and bones. </span></div>
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<span style="font-size: large;">We need Doctors to help us, we need research and compassionate people to help us!<br />
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<span style="font-size: large;">Cannot let Lyme Disease to propagate in more cities and countries;</span></div>
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<span style="font-size: large;"> you, the "wisest and powerful" are letting both things to happen:</span></div>
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<span style="font-size: large;">the infection spreading all over the body and all over the world!</span></div>
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<span style="font-size: large;">May God help us and may we find a cure to your injustice!</span></div>
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<span style="font-size: large;">I need to add that I think the small parasite that goes to the medulla could be a parasite called </span><br />
<span style="font-size: large;">"<b>Sarcocystis neurona</b>", a parasite that resembles toxoplasmosis that can be in the cat's feces. My lab test made by Clongen Laboratories reads "numerous round motile unknown organisms" ... and other elongated with dubbell heads swimming in my blood, I guess those resemble toxoplasmosis and as an article writen by Stephanie Pappas reads "they make toxoplasmosis, the disease caused by T.<i></i>gondii infection, worse. The result is brain swelling and death.". Hope researchers and scientists help with this "discovery". The blog of Dr "J" LYMEMD continusly speaks about this numerous motile round organisms that no one knows what are they. I think these are the <b>Sarcocystis neurona because the symptoms match perfectly! </b></span><br />
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<span style="font-size: large;"><b><span style="font-size: x-small;">NOTE: LYME THE ROLLERCOASTER BLOG DOES NOT OFFER, DOESN'T GIVE<span style="font-size: x-small;">, </span> NOR INTENDS TO GIVE ANY MEDICAL ADVISE NOR MEDICAL RECOMMENDATIONS.</span></b></span><span style="font-size: small;"><b> <span style="font-family: "Times New Roman","serif"; font-size: x-small;">THESE ARE JUST MY THOUGHTS, IDEAS, RESEARCH AND EXPERIENCE SHARED.</span></b></span></div>
MJhttp://www.blogger.com/profile/16614021020877246061noreply@blogger.com0tag:blogger.com,1999:blog-9207742591307790987.post-86797114783254123832011-04-18T00:37:00.000-07:002013-02-27T22:52:54.240-08:00LYME DISEASE, GETTING BETTER WITH IVERMECTIN!<h6 class="uiStreamMessage" data-ft="{"type":"msg"}">
<span class="messageBody" style="font-size: large;">Sleeping without pain, waking up with no symptoms but the "natural" cramps... <br />
Ivermectin and now Alinia together made a huge difference for me. No pain, enjoying the bed, relaxing, sleeping well, no fear of death, not the incessant exploiting inside my body, no light nor sound sensitivity, no muscle pain, no arthritis pain, no bells palsy, no heart pain!!!!! I'm still some swollen and I'm still fighting some co-infections but I am recovering, for first time in 5 years I feel a huge change! I'm not having antibiotics now, since I took the CIPROFLOXACIN I have no need of more, just antiparasitics!!</span><span style="font-size: large;"> </span><span style="font-size: large;"> I recently had Bactrim again, it is magic too!</span></h6>
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<span style="font-size: large;"> <span style="font-weight: normal;">How come some Drs and certain organizations state Bactrim or Flagyl are not good when they're maybe the only ones that really help with Lyme Disease infections? Maybe those companies are not in the top ten money makers? lol!</span> </span><span style="font-size: large;">And how come the US does not have the human version of Ivermectin sold in South America and given for free in Africa after having such zoonotic disease growing every day all over the country?</span></h6>
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<span style="font-size: large;"><span style="font-weight: normal;">Why few talk about Lyme Disease being a parasitic infection? The only word mentioned is bacteria, but it is not just that Lymies only get intestinal parasites but parasites in the blood, parasites inside the sinuses, parasites in our glands, parasites living inside our muscles and bones and of course parasites invading our brains and hearts. Yes PARASITES not "just" bacteria; that's why the bugs are "resistant to antibiotics" because they're bigger than bacteria: they are parasites! Like trying to kill snakes with flying bugs spray!<br />
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Treat the parasites and the symptoms will fade; if you don't believe me just try and see! <br />
A <b>zoonotic infection is parasitic</b>, lol, I didn't invent that, it is known everywhere in the world, scientists, medical personnel, everyone knows but the ones that treat Lyme Disease nor the ones that postulate the guidelines to treat it, don't ask me why? The illness is growing everyday but the truth is still hidden!</span> </span></h6>
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<span style="font-size: large;">Plus more than 75 % of the cases of Lyme Disease are infections of Bacteria (Borrelia Burgdorferi) and parasites (Babesia), plus other called "co-infections of bacteria and parasites like Bartonella, Erlichia, Mycoplasma and some types of viruses. So most of the Lymies have Babesia too, that is worse than having malaria. <br />
<span style="font-weight: normal;">When the blood is seen in a microscope the malaria parasites are seen invading the red blood cells, one parasite per one RBC, while the Babesia is recognized for having up to three parasites invading the red blood cells, three times the damage, three times the anemia! The other difference is that malaria parasites feed from the liver and brain, so they kill their host really fast; Babesia parasites are travelers who love to eat brain cells, heart cells, gland cells and the more they reproduce the more they migrate to other organs, nerves, muscles and bones, so the host lives longer but suffering more until dying in pain. If that is not a parasitic infection please correct me and tell me what that is???? I know a person who's child has the parasites in the sinus, brain, glands and body, but she is worried for the child having mold in the blood, can someone measure what is more damaging for a human being? why the denial of the damage parasites do to humans? </span> </span></h6>
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<span style="font-size: large;"><span style="font-weight: normal;">If you are interested in the<b> Ivermectine</b> the human version in the US is called <b>STROMECTOL</b>, needs a prescription and the treatment should be careful because the die off is truly hard. Each parasite throws a toxin when they die, plus their d</span><span class="text_exposed_show" style="font-weight: normal;">ead bodies are another toxin and of course, the medicine to kill the parasite is a poison, so what ever dose you take, multiply it by three, that is the load your body will have to deal with. So you better start low, but repeat it regularly to kill the eggs, to stop their reproduction, to clean your body form their continuous devouring you.<br />
There is a human version of Ivermectin sold in South America and other countries that come sin small bottles of 6 ml, like tear drops bottles. The dose is one drop per one kilogram. Well that for healthier people, because when the person is very infected is always advisable to start with lower doses.</span><span style="font-weight: normal;"><br />
The veterinary version is called Ivomec, Ivermax, Zimectrin and Iverchoice to mention some; these come in pastes and in liquid in huge gallons or bottles. The veterinary version is made to deworm and treat cows, horses and pigs. The concentration of it is the double of the human version or even more, so if someone decides to treat with these the amount of medicine given has to </span><span class="text_exposed_show" style="font-weight: normal;">be half of the medicine you would take in a human version. </span></span></h6>
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<span style="font-size: large;"><span class="text_exposed_show" style="font-weight: normal;">For the human dosage the liquid Ivermectina is taken one drop at 0.6% concentration per one KILOGRAM of weight ONCE A WEEK. If you are a Lymie, infected for long time you better don't start with a "normal" dose, my Doc said the best should be to start with half of it and be prepared to herx; but also be prepared to have great days, good ones, glorious ones!</span><span class="text_exposed_hide" style="font-weight: normal;"><span class="text_exposed_link"><a href="http://www.blogger.com/post-edit.g?blogID=9207742591307790987&postID=8679711478325412383"> </a></span></span></span><span style="font-size: large; font-weight: normal;"><span data-jsid="text"> If you don't repeat the anti-parasitic treatments the parasites will take over again and again!!! I mean repeat once a week or once every two weeks but never before because the medicine stays in the body during four days, so if you repeat it before that time you could be duplicating the dose and making it poisonous. One year is probably the minimum time you might need to do the treatment. I take it once a week, and will keep on doing it!</span></span></h6>
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<span style="font-size: large;"><span data-jsid="text">I had a friend taking 5 drops of Ivermectin a week, didn't help her at all, lol, too low. I heard this person stating Ivermectin didn't do much good, but the person just took one dose, felt recovery and never took it again, which means the eggs hatched and reproduced again. I saw this guy who one night took one bottle of the human liquid version (not sold in the US), then the next morning he took another full bottle of the human version (6 ml); he herxed like crazy but then he was fine, lol, he says that is the correct dose... I would not try that too much I guess. I read about this girl two years old who drank more than half a bottle of Ivermectine for cows, a huge one ltr bottle, they took her to the hospital, induced vomiting and the girl was fine... so I know it is toxic but not that is going to kill us not even taking the complete little human version bottle. It is safe for humans, but the herx is bad the more bugs it kills. I found a very recognized Doctor is treating with 12 mgs a day of human Ivermectin every day for two weeks, I found this a strong dose but that is just my personal opinion not a medical advise. My Doc from my home country told me that the medicine is not cleared up in our bodies in four days so dosages must not be repeated before to not multiply the treatment. I mean if you took 12 mgs today - which is very high in my opinion, and tomorrow you take another 12 mgs you would be having 24 mgs of medicine in your body because the body cannot clear it so fast, so if you do this everyday non stop for two weeks well, I think it could be poisonous unless you are sure your body can take such huge doses. My Doc advised me to take half the dose once a week and raise it up little by little, better a long treatment but slow. Also because each parasite that dies releases a toxin which makes us very sick, so the parasite killing has to be slow and regular!</span></span></h6>
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<b><span style="font-size: large;"><span data-jsid="text"><span style="font-weight: normal;">Denying the parasitic infection in Lyme Disease is condemning the people to never recover and suffer, or maybe that is what they want to make more money and sell more medicines? Hope not, honestly pray it is not just business!</span></span></span></b></h6>
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<span style="font-size: large;"><span data-jsid="text"><span style="font-weight: normal;">NOTE: I didn't know that the parasites in blood like with the malaria and Babesia they travel not only to the organs but go hide to the tips of the fingers and ears. So last week when I went to the lab of the hospital they didn't see the parasites in my blood and I was surprised because I have seen them in my microscope at home. The difference was they took my blood from the big vein of the hand while I took the sample from the tip of my finger!! </span></span></span></h6>
<span style="font-size: large;">:)</span><br />
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<span style="font-size: large;"><span data-jsid="text"> </span>No one pays me a penny for posting my information, for researching, for trying, for sharing. I don't lead anyone nor any interest, I don't follow anyone nor any company. I suffered the most horrible nightmare and I beg God to help me and I promised Him I will share all I learned on my way back to recovery, and I have done it and will keep on doing it.<span data-jsid="text"> </span></span></h6>
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<span style="font-size: large;"><span data-jsid="text"> If you use my information, please give me the credit, don't post it in your private blog like if you researched it, or you found it or you had the idea of it; just be fair as I always post the links and info too. </span></span></h6>
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<span style="font-size: large;"><span data-jsid="text"><span style="font-weight: normal;">I am on my way to recovery but not thanks to the ten Doctors that dismissed me, nor I can thank the one LLMD who nicely treated me because he also denies the parasitic part of the infection; if I were in any of their hands I would be quadriplegic and with dementia or dead after horrible suffering. I'm alive, surviving, almost doing good thanks to God who guided me, to my family Doctor in my home country in South America who I called and who trusted me after not seeing me in more than ten years, but his great heart and lots of knowledge were generous enough for trying to help me, and to my family my cousins and friends who brought me medicines and my closed family who had taken so much care of me. </span></span></span></h6>
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<b>Sorry, these Doctors had the opportunity to make a difference but their egos were as big as their ignorance. </b></span></span></span></h6>
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<span style="font-size: large;"><span data-jsid="text"><span style="font-weight: normal;"> THIS IS JUST MY OPINION NOT A DOCTORS ADVISE.</span></span></span></h6>
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<span style="font-size: large;"><span data-jsid="text"><b><span style="color: #6aa84f;"><span style="font-weight: normal;">Thanks for sharing!</span></span></b></span></span></h6>
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<span style="font-size: large;"><span data-jsid="text"><b><span style="color: #6aa84f;"><span style="font-weight: normal;"> </span></span></b></span></span></h6>
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<span style="font-size: large;"><b><span style="font-size: x-small;">NOTE: LYME THE ROLLERCOASTER BLOG DOES NOT OFFER, DOESN'T GIVE<span style="font-size: x-small;">, </span> NOR INTENDS TO GIVE ANY MEDICAL ADVISE NOR MEDICAL RECOMMENDATIONS.</span></b></span><span style="font-size: small;"><b> <span style="font-family: "Times New Roman","serif"; font-size: x-small;">THESE ARE JUST MY THOUGHTS, IDEAS, RESEARCH AND EXPERIENCE SHARED.</span></b></span></h6>
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MJhttp://www.blogger.com/profile/16614021020877246061noreply@blogger.com0tag:blogger.com,1999:blog-9207742591307790987.post-31047893118396746732011-02-01T18:34:00.000-08:002011-02-02T00:27:15.088-08:00LYME DISEASE, PLEASE DONATE IVERMECTIN TO THE US; CHARITY STARTS AT HOME!<div class="MsoNormal" style="line-height: normal;"><span style="font-family: "Times New Roman","serif"; font-size: large;">This is the letter I just sent to MECTIZAN, the invaluable program made by Merck to help eradicate illnesses in Africa and third world countries by donating them <b>Ivermectin</b> and treating ill people who are suffering with river blindness also called Onchoneariasis,</span><span style="font-family: "Times New Roman","serif"; font-size: large;"> and Lymphatic filariasis. <b> </b></span></div><div class="MsoNormal" style="line-height: normal;"><span style="font-family: "Times New Roman","serif"; font-size: large;"><b>I ask them to please bring their Ivermectin to the US and Europe to help to eradicate Lyme Disease, the biggest zoonotic infection of the century. </b></span><span style="font-family: "Times New Roman","serif"; font-size: large; line-height: 115%;"><b>Borrelia is just one of the many bugs transmited by the tick, and just that one is a malaria like bacteria, but we are also devoured by Babesia a ferocious parasite, we also have nematodes - filarial infections - and co-infections like Bartonella, Erlichia, and the cherry on top of the pain are viruses like Epstein Barr or Mononucleosis. Isn't this too much for one person to take? more without proper medical treatment?</b></span></div><div class="MsoNormal" style="line-height: normal;"><span style="font-family: "Times New Roman","serif"; font-size: large;"><b><br />
</b></span></div><div class="MsoNormal" style="line-height: normal;"><span style="font-family: "Times New Roman","serif"; font-size: large;">This is my letter, hope they not ignore it!</span></div><div class="MsoNormal" style="line-height: normal;"><span style="font-size: large;"><br />
</span></div><div class="MsoNormal" style="line-height: normal;"><span style="font-family: "Times New Roman","serif"; font-size: large;"> "HELLO<br />
MY NAME IS MARIA P. J. I LIVE IN FLORIDA, I HAVE LYME DISEASE.<br />
It is terribly painful to see the people of this same country is not being helped dying in so much pain while suffering the biggest infection of the century, Lyme Disease is not cured with just two weeks of Doxycycline, </span><span style="font-family: "Times New Roman","serif"; font-size: large;"> this is a multi-parasitic, poly bacterial infection requires years of antibacterial and anthelmintic treatments,<br />
in fact still no one knows the cure for this never ending nightmare. </span><span style="font-size: large;"><b><span style="font-family: "Times New Roman","serif";">We need serious help!</span></b></span></div><div class="MsoNormal" style="line-height: normal;"><span style="font-size: large;"><br />
</span></div><div class="MsoNormal" style="line-height: normal;"><span style="font-family: "Times New Roman","serif"; font-size: large;">Our symptoms go from all the Lymphatic system affected - very similar to your treated lymphatic filariasis, to heart, brain, liver, kidney swollen, infected and failing, and all the other symptoms of the malaria and flu like illnesses; yes we do have bugs coming out of our skin or eyes like in the river blindness; plus we got muscle pain as in fibromyalgia, joint pain as in arthritis, and symptoms like Parkinson’s, Alzheimer’s disease and many neurological like extreme pain in nerves of the legs and or hand, loss of smell or increase sound or light sensitivity, etc. It is an interminable list that most Doctors don't want to hear nor treat and that to stop the winning they just prescribe an anxiety reliever or a pain killer. </span></div><div class="MsoNormal" style="line-height: normal;"><span style="font-size: large;"><br />
</span></div><div class="MsoNormal" style="line-height: normal;"><span style="font-family: "Times New Roman","serif"; font-size: large;">You are treating illnesses that the world ignored before, you have the power and the medicines; Lyme Disease is the most dismissed and ignored illness of the US and time will show how much it has spread to certainly become a pandemic because it is out of everyone's control. I have friends in Finland or Germany all suffering the same symptoms. I got the infection here in Florida, CDC states it is not here; it is my health and my life against CDC. Doctors won't treat it or doesn’t know how to do it, nor even the so called "specialists", the Infectious Disease Doctors don't treat LD. There are some "new" Doctors who call themselves LLMD - Lyme Literate Doctor who are creating their own protocols and charge one eye of the face to see a patient...</span></div><div class="MsoNormal"><span style="font-size: large;"><br />
</span></div><div class="MsoNormal"><span style="font-family: "Times New Roman","serif"; font-size: large; line-height: 115%;">My Doctor in Colombia gave me IVERMECTINA in drops; it made the difference, not cured me but put me on my way to recovery. One now very famous “American Doctor” who treats "successfully" LD has IVERMECTIN in his “secret protocol” combined with Albendazol and Alinia.. yes, he is the only one "curing" the disease! <b> Ivermectin is for parasites, protozoans, filarial infections, nematodes, we have those and more... </b></span></div><div class="MsoNormal"><span style="font-family: "Times New Roman","serif"; font-size: large; line-height: 115%;"><b> </b><br />
How can I get that IVERMECTINA TO HELP HEAL MY 450 FRIENDS OF FACEBOOK<br />
AND THE 2,800 FRIENDS MY FRIEND TIM HAS IN HIS FB GROUP ALL SICK WITH LYME DISEASE? </span></div><div class="MsoNormal"><span style="font-family: "Times New Roman","serif"; font-size: large; line-height: 115%;"><br />
You have the medicine; you have the power of helping us, please do it!!!!!</span></div><div class="MsoNormal"><span style="font-family: "Times New Roman","serif"; font-size: large; line-height: 115%;"><br />
HOW CAN YOU DONATE US MEDICINE OR TREAT US?<br />
IS THERE ANY WAY WE CAN BUY IT FROM YOU? WE CANNOT BUY IT HERE IN THE US!<br />
<b>Please consider helping us in any possible way!<br />
</b><br />
IS THERE ANY HOPE FOR US?<br />
Come share with my group and see how big this problem is, and how hard our lives are; if this is not the purgatory or hell I don't know what it is!<br />
<br />
Thank you for your time and attention.<br />
Best regards,<br />
<br />
<br />
MARIA P. Juan."</span></div><div class="MsoNormal"><span style="font-size: large;"><br />
</span></div><div class="MsoNormal"><span style="font-family: "Times New Roman","serif"; font-size: large; line-height: 115%;">Read about the amazing program Merck does at Africa and other countries, hope they do that here in the US: </span></div><div class="MsoNormal"><span style="font-size: large;"><a href="http://www.mectizan.org/history">http://www.mectizan.org/history</a></span></div><div class="MsoNormal"><span style="font-family: "Times New Roman","serif"; font-size: large; line-height: 115%;"> </span></div><div class="MsoNormal"><span style="font-family: "Times New Roman","serif"; font-size: large; line-height: 115%;">COPY RIGHT INFORMATION 2011 </span><span style="font-family: "Calibri","sans-serif"; font-size: large; line-height: 115%;">©</span></div>MJhttp://www.blogger.com/profile/16614021020877246061noreply@blogger.com0tag:blogger.com,1999:blog-9207742591307790987.post-3215050534854517382011-01-17T04:01:00.000-08:002013-02-27T22:56:08.809-08:00LYME DISEASE, DEVOURED BY PARASITES<!--[if gte mso 9]><xml> <o:OfficeDocumentSettings> <o:AllowPNG/> </o:OfficeDocumentSettings> </xml><![endif]--><!--[if gte mso 9]><xml> <w:WordDocument> <w:View>Normal</w:View> <w:Zoom>0</w:Zoom> <w:TrackMoves/> <w:TrackFormatting/> <w:PunctuationKerning/> <w:ValidateAgainstSchemas/> <w:SaveIfXMLInvalid>false</w:SaveIfXMLInvalid> <w:IgnoreMixedContent>false</w:IgnoreMixedContent> <w:AlwaysShowPlaceholderText>false</w:AlwaysShowPlaceholderText> <w:DoNotPromoteQF/> <w:LidThemeOther>EN-US</w:LidThemeOther> <w:LidThemeAsian>X-NONE</w:LidThemeAsian> <w:LidThemeComplexScript>X-NONE</w:LidThemeComplexScript> <w:Compatibility> <w:BreakWrappedTables/> <w:SnapToGridInCell/> <w:WrapTextWithPunct/> <w:UseAsianBreakRules/> <w:DontGrowAutofit/> <w:SplitPgBreakAndParaMark/> <w:EnableOpenTypeKerning/> <w:DontFlipMirrorIndents/> <w:OverrideTableStyleHps/> </w:Compatibility> <m:mathPr> <m:mathFont m:val="Cambria Math"/> <m:brkBin m:val="before"/> <m:brkBinSub m:val="--"/> <m:smallFrac m:val="off"/> <m:dispDef/> <m:lMargin m:val="0"/> <m:rMargin m:val="0"/> <m:defJc m:val="centerGroup"/> <m:wrapIndent m:val="1440"/> <m:intLim m:val="subSup"/> <m:naryLim m:val="undOvr"/> </m:mathPr></w:WordDocument> </xml><![endif]--><!--[if gte mso 9]><xml> <w:LatentStyles DefLockedState="false" DefUnhideWhenUsed="true"
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<span style="font-size: large;">Imagine, how can some Doctors consciously decide to not treat parasites like if it is something that could be ignored? Can it be ignored?<span style="font-size: large;"><span style="font-family: "Calibri","sans-serif";"><b> </b></span></span></span></div>
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<span style="font-size: large;">Some physicians add the anti-parasitic treatment at the end of their "protocol" and miracle, the person starts their way to recovery,what a coincidence? My friend fellow Lymie told me that after reading my info she asked her LLMD about testing her parasites and he answered:<span style="font-size: large;"> </span><b>"what for? no matter what we can find I am not going to change the protocol". </b></span></div>
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<span style="font-size: large;">Can this be medicine we are talking about?<span style="font-size: large;"> Ignoring the parasitic component in Lyme is a cruelty, and treating this multiinfection only with antibiotics is ignorance! Some think the<span style="font-size: large;">yre treating the parasites with antibiotics, really? It is</span> li</span>ke trying to kill a snake with flea spray? how many bottles of spray and years of treatment it might require? <span style="font-size: large;">You think </span>we might kill her one day? </span></div>
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<span style="font-size: large;">The theory of the parasites feeding the bacteria for them to eat it later sounds nice and some might believe it or not, but the reality is that generally where there is a parasite there is bacteria around, simple. They have a proper ecosystem where they maybe feed from us and not from each other? theories that can be disputed or argued but a scientific reality that shows that both types of bugs, in fact more than two or three types of bugs are living inside us, feeding off from us every day, reproducing and killing us slowly. They start in the blood, then go to the glands and lymphatic system, then the brain, travel through all the Central Nervous system and then they go to the heart;and when they are so many they migrate to other organs, to the bones and muscles; they are inside our skin and our eyes and scalp. Who is feeding who and how? Is it really a choice to not treat such infection or is it absolute ignorance and why not,<b> negligence and cruelty?</b></span></div>
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<span style="font-size: large;">Imagine our bodies devoured by thousands if not millions of different bugs for weeks, months, and then for years and years? </span></div>
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<span style="font-size: large;">Imagine the pain,the palpitations, the fear, the not knowing what is next, and every day every time is worse, there is no recovery, no reverse. </span></div>
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<span style="font-size: large;">Would you have hope? Hope if you cannot read, if the light hurts you, if the sounds kill you, if you cannot move, if food has no taste, if everything smells bad, if your muscles fell off the bones, if the bones cannot hold you, if your nerves are so tight they hurt you worse than an electrocution; if your heart races and then stops... I thought I was not going to survive the first day; that night I said my goodbyes... yes antibiotics helped me, but didn't cure me, because parasites don't die with that type of medicine; I just start to get better after I had Flagyl and then Ivermectin; is that too much to ask?</span></div>
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<span style="font-size: large;">IS IT TOO MUCH TO ASK TO THE MEDICAL STAFF TO TREAT THE PARASITES AS LONG AS IT IS NEEDED,WHEN INFECTED WITH LYME DISEASE?</span></div>
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<span style="font-size: large;">IS IT TOO MUCH TO ASK TO PLEASE NOT IGNORE THE SEVERITY OF THE DAMAGE BACTERIA AND PARASITES CAUSE INSIDE OUR BODIES?</span></div>
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<span style="font-size: large;">This article and the responses to it could be very helpful to treat Lyme Disease: </span></div>
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</style> <![endif]--><span style="font-family: "Calibri","sans-serif"; font-size: large; line-height: 115%;"><a href="http://www.latitudes.org/forums/index.php?showtopic=11618&st=0&gopid=99378&#entry99378">http://www.latitudes.org/forums/index.php?showtopic=11618&st=0&gopid=99378&#entry99378</a></span></div>
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<span style="font-size: large;"><b><span style="font-family: "Calibri","sans-serif"; line-height: 115%;">Thank you for sharing with me this journey of suffering and knowledge!</span></b></span></div>
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<span style="font-family: "Calibri","sans-serif"; font-size: large; line-height: 115%;">M.J. </span><br />
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<span style="font-size: large;"><b><span style="color: #0c343d;"><span style="font-family: "Calibri","sans-serif"; line-height: 115%;"><span style="color: black;"> Note: the more I read, and the more I learn from all my 2000 friends, the more <span style="color: #0c343d;">I</span>'m convinced Lyme is parasitic and should be treated as such. As I posted in 022813, treating parasites with antibiotics is like trying to kill snakes with flea spray! Please!</span></span></span></b></span><br />
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<span style="font-size: large;"><b><span style="font-size: x-small;">NOTE: LYME THE ROLLERCOASTER BLOG DOES NOT OFFER, DOESN'T GIVE<span style="font-size: x-small;">, </span> NOR INTENDS TO GIVE ANY MEDICAL ADVISE NOR MEDICAL RECOMMENDATIONS.</span></b></span><span style="font-size: small;"><b> <span style="font-family: "Times New Roman","serif"; font-size: x-small;">THESE ARE JUST MY THOUGHTS, IDEAS, RESEARCH AND EXPERIENCE SHARED.</span></b></span></div>
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MJhttp://www.blogger.com/profile/16614021020877246061noreply@blogger.com0tag:blogger.com,1999:blog-9207742591307790987.post-6799830065828953762010-10-31T08:42:00.000-07:002011-02-15T04:41:18.728-08:00LYME DISEASE IS A PARASITIC INFECTION! Borrelia Burgdorferi is a small PARASITE, transmitted by a tick, that initially invades the blood of the human and from there it travels to different organs and tissues of the host. Borrelia is a parasitic infection not just a bacterial infection, unless bacteria is looked at as a small parasite. I have not read an article or a message anywhere that states this I have said here above; every where it is said that Borrelia is a "Bacteria" and it is not specified that it is an intracellular bacteria, meaning a parasite.<br />
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Of course by treating Borrelia as a bacteria the management of the parasitic infection might not be adequate or sufficient and the parasite might be having options to survive better and to even kill the host. Not saying that Lyme Disease might also have parasitic co-infections is another negligence that must be addressed to save the lives of many people..<br />
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Simple observation leads to the obvious conclusion, no need to be a scientific: "Intracellular parasites, such as bacteria or viruses, tend to rely on a third organism which is generally known as the carrier or vector. The vector does the job of transmitting them to the host." Parasites, meaning big bugs, meaning bugs that can grow and act very different from a small almost invisible bacteria: " Parasites evolve in response to defense mechanisms of their hosts" - this is not an act of an insignificant organism!<br />
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Borrelia is transmitted by a tick the same way as the "Plasmodioum" is transmitted by the mosquito when it generates the illness we call Malaria - in the endemic areas of Colombia we call it "Paludismo", same thing. When the tick bites his saliva spreads the bacterial and parasitic infections, as any other infections caused by a vector, meaning by an insect or a spider; that is why Lyme Disease is called a "Vector- born Disease". This is CDC explanation about it: "The term “vector” refers to any arthropod that transmits a disease through feeding activity". See? transmits a disease but the difference here is that it doesn't transmit a simple fever that goes away with two weeks of treatment; the American TICK transmits a multi-parasitic and poly bacterial infection that causes a severe septicemia invading blood, organs, brain, bones, lymphatic system, circulatory system; feeds of tissues like the heart and the kidney and doesn't kill the host until years of pain and suffering.<br />
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And again, symptoms caused not only by a bacteria but by a parasite that evolves and responses to a treatment in a very different way than a regular bacteria; this is a protozoan that goes inside the cell or runs outside depending on the conditions; it is a little animal surviving and feeding from our tissue. Plus, because it is a strange body inside our body, bacteria is produced around it and this becomes a mini ecosystem inside the human body where the bacteria feeds off of the left overs of the parasites, and the bigger bugs hide behind the bacterial infection; multi parasitic - poly bacterial, plus viruses interacting, all together devouring everything around and moving and setting their camps in different places of the body. It is said that Borrelia even jumps inside the white blood cells that come to attack her so now the immune system is infected and is taking that infection to other parts of the body, plus it becomes unable to kill the infection unless destroying itself... if this doesn't sound like madness I don't know what is!<br />
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Tell me, is this something everyone knows and I don't? Is it that I am just "discovering the hot water"? If so, why every article about Lyme Disease states it is a "bacterial" infection and why it is not publicly said that Borrelia Burgdorferi is really a PARASITE transmitted by a tick - some say it is also transmitted by lice and flies, I don't know. Yes, a parasite that comes inside the body of the human being when bitten by the tick, something so obvious as it is said when the malaria is transmitted. Why this incredible obvious truth is denied? just to neglect the reality that the US has a parasitic infection as severe or more like the third world countries diseases? is it possible to hide a piece of this truth to soften the cruel reality and to maintain power? Or it is said everywhere that Borrelia is a bacteria, to not scare the public? LOL? Where in the world can a parasitic infection can be hidden and denied like if it won't hurt or won't hurt so bad?<br />
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If, in fact, a bacteria transmitted by a host, called an "intracellular bacteria" is a parasite, but small, that type of organism will require a special treatment, to eradicate it, to kill it, different from a regular bacteria acquired by, for example, a cut or a pinch in a finger? and this, again obvious reasoning will bring to question why, Borrelia Burgdorferi, such intracellular bacteria that lives and functions as any other big parasite is being medically treated with just two weeks of a regular antibiotic like if this will be enough to kill such complicated organism? Have you heard of people getting cured of malaria after receiving two weeks of Doxycicline or Amoxacillin? so why the ones infected with Borrelia Burgdorferi, a very well known smart parasitic organism, are treated as if they just had a minimal regular infection?<br />
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More over, if the time has shown that the tick bite transmits not only Borrelia, who now we know it is a parasite, but also Babesia, an old recognized ferocious parasite and simultaneously the saliva of the tick also spreads other bacteria and co-infections such as the terrible Bartonella, Erlichia, Rickettsia - the causative of thyfus fever - and various viruses, how come this is treated like a regular infection, if this is a deadly bomb?<br />
Read what CDC states: "Lyme disease is a tick-borne illness caused by infection with the bacteria <i>Borrelia burgdorferi</i>." "The bacteria that cause Lyme disease are transmitted through the bites of infected ticks." "Within days to weeks following an infectious tick bite, most patients (about 80%) develop a red rash called an erythema migrans (a.k.a., “EM” or “bull’s-eye” rash) around the bite site. This rash slowly expands (up to 12 inches in diameter and clears around the center, but does not itch. It is usually accompanied by general tiredness, fever, headache, stiff neck, muscle aches, and joint pains. If untreated or not properly treated, some patients may develop arthritis, neurological problems, and/or heart problems weeks to months later. " "When Lyme disease is detected early, it is treated with oral antibiotics such as doxycycline or amoxicillin and treatment usually lasts for 10-21 days. In the later stages of Lyme disease, antibiotic treatment lasts longer, is more complicated, and patient response to treatment is slower." ... how can they be so far from the reality we Lyme Disease patients live? 10 days of treatment for what?<br />
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I am no expert in medicine nor in infectious diseases nor in bugs but I just ask since when or where in the human medical history parasites are killed with two or three weeks or Amoxacillin, or Doxycicline? No need to know a little better than that, the logic states that bigger bugs need antihelmintics or vermifuges not just antibiotics.<br />
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Just this recommendation from the wise, from the experts in avoiding the proliferation of infectious diseases in the US is a wrong beginning. Why would CDC ignore a parasitic infection and call it and treat it as a bacterial infection? It is also scary to read that CD states that "Spread of the Lyme disease bacteria from an infected tick to a person is not likely to occur unless the tick has been attached to the person’s body for at least 36 hours."... not true! The tick bites and in it's mouth is the contaminated saliva, and it is passing it at the same time and as soon as it starts sucking the blood from the host. What logic states that the bacteria takes 36 hours to pass to the human body? if the same CDC states that the infection could be spread just by trying to detach the tick, just by touching it with the bare hands, something immediate, imagine what can come every second the tick is attached sucking blood?<br />
By the contrary of what CDC states, experience has shown that everyone bitten by an infected tick gets the infection and needs to be urgently treated, so ignoring it is a parasite and then the severity of the fast transmission of the infection is another serious imprecision that causes an increase in the lack of proper, adequate treatment.<br />
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Now, has anyone seen a Borrelia? some have pictures of it taken by microscopes or using special magifying lenses; but someone has seen a Borrelia when it evolves and grows and invades the intestine and other organs of the human body? why it is said that Borrelia is so hard to see and to study if it is a parasite and by being this type of organism you can see it with your "bare eyes", easily! Not when it is hiding in the blood, nor inside the tissues but when it evolves to a regular worm life and goes to the intestines for example, it can be seen and studied, like another regular big bug. Is this new to medicine or maybe this is the result of the absolute denial of the US when affirms that there are not parasites in this country? and this ignorance covers the possibility of treating and curing the sick people suffering with parasitic infections?<br />
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If Borrelia is not hidden under the false idea of a bacteria, stool sample tests could be finding Borrelia and adequately treating patients according to their level of infection. Is this new to science again? The similarity of the intestinal parasites expelled after receiving proper treatment, with the Borrelia shown inside the blood are shocking; the bug maintains it's shape but can grow to one or two inches, passing from being an almost invisible bacteria to a big powerful worm. This is shocking news; prove me wrong!<br />
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Now, It is finalnally said that 40% of American ticks transmit "nematodes" which are parasites, some call them worms. Studies state thet Dr Willi Burgdorferi, who discovered the Borrelia, found 30 types of microfilarial worms in an adult tick, which might lead to conclude that if people is indeed infected with various types of parasites the treatment with just antibiotics given from 2 to 4 weeks is not going to clean the infection. This certainly is the answer of why ill people relapse and cannot get completely cured. Those cases cataloged as "Chronic Lyme Disease" could be just cases of people who have parasitic infections not properly treated.<br />
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<b>It seems to me that by denying that Lyme Disease is a parasitic infection the wise are denying at the same time proper treatment, proper diagnoses, proper lab test, proper and adequate cures and medicines desperately needed.</b><br />
<b>Hope Lyme Disease patients are treated correctly and cured; yes cured, because no matter how many say there is no cure for Lyme Disease yet, until someone treats it like what it is, a parasitic infection with bacterial co-infections. Amen.</b><br />
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Wikipedia <a href="http://en.wikipedia.org/wiki/Parasitism#Types_of_parasitism">http://en.wikipedia.org/wiki/Parasitism#Types_of_parasitism </a>MJhttp://www.blogger.com/profile/16614021020877246061noreply@blogger.com1tag:blogger.com,1999:blog-9207742591307790987.post-39683649894621040882010-03-20T01:25:00.000-07:002010-07-11T02:59:12.071-07:00IVERMECTIN FOR LYME DISEASE!This, again, is just my opinion and my experiences as a Lyme disease sufferer. Would like to start saying that each person reacts differently to the treatments and that I have not found the miraculous cure yet, but there is hope, big hope now!<br />
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I was thinking on answering to a Facebook friend my thinking and experience with "IVERMECTIN"; but decided to do a blog about it because I'm having many requests about the topic, lol; I'm the "expert here"? No way!!!! But I'll try my very best because I do want to share my experience thinking it might be of some help!<br />
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Before starting let me say that I was going to say to my friend that precisely because we get to that point of desperation we become more resourceful and even creative. I was saying to her: "I guess sometimes we have to do things according to how desperate we are and that sometimes pushes us further or at times could make us crazier?<br />
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Well my Ivermectin story of course is product of desperation. I would have to tell my story with the Doctors and the treatments I have had already to finally get to the "Ivermectin chapter"! do I need to confess it all?<br />
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Being with a disease ten Doctors dismiss, facing death every day in pain and fear and seeing there was no hope, no care, no probabilities, well, if that doesn't make you "creative' what does? The instinct of survival is wonderful, so as many of you, I did research and found people suffering symptoms like me; so many they were innumerable. I went to this "Infectious Disease Specialist" (Doc number nine), after I "suspected Lyme, and gave him my "reduced list of symptoms", just 21... the tingling or twitching or even the bells palsy where not included.... and of course he said that "for sure I had no infection at all, but probably an allergy"... God bless the guy, ha.<br />
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Desperation plays a very crucial game in Lyme because it makes us so strong we move even though we can barely hold tight. So I started by understanding the cause of Lyme disease? Bacteria. No, it is not accurate. The word "BACTERIAS" in English doesn't exist, but it should have an "S" at least to describe Lyme Disease. So, because of this linguistic thing I found: multi-bacterial syndrome; more accurate right? But not complete, why? Because the tiny tick seems to transmit more than just many bacteria (s). It is not that the person MAY have "co-infections". The "may have; might have" is the second linguistic trick that is stopping Doctors and our selves to be treated properly and on time and are pushing us far from recovery!!!! <b>Lymies have co-infections, </b>not every case have the same bugs; but weird not to find multi or poly bugs inside a Lymie! <br />
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<b>Co-infections</b> of what or how?<br />
<ul><li> Found that <b>Bartonella </b>is a kind of bug. Not a parasite, not a bacteria, it is it's own specie. It "jumps" to the blood and swims freely in it's host. This little round motile bug seems to attack the brain and the neuro-cognitve functions... has to be killed to improve; no way to co-host-share the space with this one! Strong medications are needed and you feel the "effect' of the fight inside our body when killing this one; it's certainly a terrible war, but you have to know you would win. Cipro is good but Bactrim was my angel... the swelling came down, even lost five pounds of "liquid" in about a week!!! Yeah, have to fight her hard!</li>
</ul><ul><li>Found that <b>Borrelia</b> is a bacteria indeed but has certain "intelligent" ways of surviving that some antibiotics won't kill her; other help her to hide inside the cells and some might hurt her. Even though it is a bacteria it is similar in something to Malaria. I don't know why it is called "malaria like", because Malaria goes to the liver and kills the host fast; or goes to the brain and the damage is very notorious and fast. Borrelia seems not to have a "favorite place' but all the body. Muscles, bones, glands, circulatory system, heart, brain...? I really don't know scientifically this, just my conjectures... In my thinking if Borrelia was as malaria I would be dead long time ago, and unless this is a dream I'm still here. So, I define my enemy as a very powerful but one that is giving me more time to give it a fight. Until we are not treated and we get to the worse case scenario where desperation is our closest friend, meaning let's try to get to the point. Borrelia doesn't die with two weeks of antibiotics, it is not totally killed not even with the most powerful medicine of the GALAXY in such a short time; we need really long term treatments. </li>
<li><b>My answer for when I hear that long term antibiotic treatment is "not good", I just ask, but long term bacteria and parasites are better?</b></li>
<li>It is a personal choice, but hey, when you get to desperation you'll understand the only choice is killing those bugs as long as it takes; or they kill the host. There's no linguistic nor political arguing there; it is a no reverse discussion. To treat or let die!</li>
</ul>WHAT HAPPENS TO SOMEONE FULL OF BACTERIA INSIDE THE BODY, IN EVERY PART AND EACH ORGAN AND IT IS NOT PROPERLY TREATED DURING YEARS AND YEARS?<br />
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<ul><li><b>Babesia</b>: this other bug inside us is a bigger one; meaning, in size and weight is bigger so it does lots of damage and just trying to get rid of it is harder and when it dies it leaves pieces so big they might hurt us worse, so we cannot kill as many but not as little so they won't have time to reproduce... etc. Babesia is a parasite, how should we get rid of parasites? It is also called a "malaria like parasite"; so, Borrelia is bacteria malaria like and Babesia is parasite malaria like; all relatives? Meaning, all dangerous to human life spread by an animal and hard to control, detect and treat?</li>
<li>Can talk about Erlichia, viruses and so many others that come with Lyme, but I'm not an expert and just wanted to "slightly picture" what was gong on inside me or inside my Lymie friends...?</li>
</ul>So after having antibiotics - tried so many -, getting different reactions; getting better and worse and living in a "Rollercoaster" I found that I was not going anywhere. Every time the lift was good but the downfall was faster, worse and deeper. I thought something was missing, so after finally being tested and properly diagnosed last year I found the lab tests showed the <b>Borrelia, first place, then Babesia "WA1" and also two more bugs swimming in my blood. </b> The lab test reads that a small round motile microorganism is present in my blood and also other type of bugs 'elongated" ... ewwwwww? oh yeahhhhhhhhhh; real reality that I have not been fighting! my God, I had four different types of bugs and was not having treatment against them, woww! How could I survive to that? God is big certainly!<br />
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WHAT HAPPENS TO SOMEONE ANYWHERE IN THE WORLD WHO IS INVADED BY PARASITES AND NOT TREATED? ANY HUMAN BEING OR ANIMAL?<br />
<ul><li>After Dr. "J" diagnosed me he gave me Biaxin but taking it was a bomb to my chest and heart... so much pain, so I asked him to change it to <b>Bactrim</b> to try. Wow... it was like a "cure"... it was not a 100% but just the first relief it gave me I have not felt it in years... I cried of happiness and thankfulness and hope! ... Had Bactrim and combined it and found it was not good; just Bactrim and Amox. were good together!!! Bactrim took my swelling away, Bactrim did kill the bugs but didn't hurt me. Anyways I was eager to "jump" to <b>Flagyl</b> to kill bigger bugs so tried them together and was terrible so keep on the Bactrim for another month and started Flagyl and still had antibiotics until just had the Flagyl alone and start feeling good and better, but then again a downfall but slower... my declining was not as strong...!! WOW. I thought I was finding some real help, so I decided to try the Ivermectin and this is the story why and how I am doing it:</li>
</ul><br />
<ul><li>IVERMECTIN: I heard about this medicine when I was living in my home country Colombia, South America ( have to clear it because some think it is in the district of "Columbia", lol). I remembered a TV ad about "IVOMEC" a veterinary medicine given to cattle, horses and I guess also for pigs, to de-worm them. I remembered it say something like "against worms and parasites"... yeah, we become creative, mooo! </li>
<li>As I said before, I had call my Doctor in Colombia, finally found him after more than ten years without seeing him and lucky me, he still <b>trusted</b> me and without seeing me or testing me he decided to help me. He first did with the antibiotics so this time when I asked about <b>Ivermectin </b>he had all the answers: he said IT IS BEING USED IN HUMAN SINCE 1990; he said it is proven to really cure the most advanced cases of "poly-parasitic infections and malaria"; he used words like "multi-bacterial infections" - I thought that's me!!!!</li>
<li>I asked Dr. Q. about IVERMECTIN in cases of Lyme Disease. He has not treated patients with Lyme Disease but he has treated thousands of patients with bacteria, parasites, worms and mostly every type of possible infection alone or combined. He said they are doing studies in Colombia demonstrating the benefits of this medicine in these extreme cases and even in the simple ones like just a kid having "lice" in it's head - the use it topic here. </li>
<li>Dr. Q. stated Ivermectin was a medicine now produced for humans, not just veterinary - so the concentration of the product changes and the bottles are smaller; ha... the cattle or horses ones are huge bottles of litters of medicine, the human presentation is a little bottle like the eye drops bottles! I looked for it everywhere in he US and I couldn't find it, just the veterinary presentation. Then I found some pills, three for $35 dollars/ something crazy. And one single dose as many state in the US or Europe is not enough, it simply won't work. I finally got the drops from Colombia; my family and friends have literally saved my life so many times now; I'm in eternal debt!!!!</li>
<li>What is and how it works? My theory? ha! Being a veterinary medicine was the good beginning of Ivermectin because medicine for animals is supposed to cure them because sick animals mean money loss; the opposite with humans because when we are sick we produce money to pharmaceuticals and everyone in the medical field... so my thinking is that Ivermectin is produced to kill bugs; many and in the fastest easiest way. We don't need big pharmaceuticals to copy it and produce it at costly prices to "cure' Lymies... hope...</li>
<li>Dosage? Dr. Q. said it depends on the infection and the reaction. The general rule is one drop per KILOGRAM of weight. Remember US pounds are just 450 gr; in the rest of the world 500 gr is a pound. So a kilogram is one thousand grams. Don't mean to be confusing, just want you to look carefully to learn your weight in kilos not American pounds. I wanted to start big and I took more drops the first time... bad joke! It was really awful! I called the Doctor and confessed my sin... he asked me to <b>cut the dose in half for next time and during the first month</b>. So I started again with less drops, half my kilos. Took the Ivermectin that day and nothing else, any other medicine. Felt a little tingling - I know.. - later on a little blurry vision and then, hours later nothing... NOTHING BAD.... like everything fine? Could this be possible?</li>
<li>Dr. Q. stated that most times after the THIRD treatment patients feel so good they sometimes stop the treatment thinking they're cured. I though, not my case; this roller coaster has been with me now for almost five years I don't think a third treatment could make such difference... well... if I say it did it could sound like a plot? I'm not selling the product and don't let anyone use my words to sell it to you or anyone; copy righted ok??? My experience is that after the third treatment I just know I start feeling HUNGER... hunger that I have not felt since 2005 - 5 years now? Hunger that felt painful at first because I couldn't recognize the feeling, ha... I was hungry for first time in years and I was so hungry it hurt, and I had to eat right away what ever, but then I was extremely happy with this feeling. The awesome part was that the FOOD TASTED GOOD TOO and that was also unknown!!!!</li>
<li>I found out that the first two or three days after I take the Ivermectin are not the very best, but are not as bad as the horrible herxes I've suffered with many treatments. They are not the best days but are decent ones. The I have some good days and even glorious super good days!!! I have been able to work and to eat and to party and write and dream, and sleep. I smell right, taste right and read fine! I am still not cured and my heart reminds me of it a lot, but boy I am having such better days!</li>
<li>For first time I am not just feeling better, I dare to say I am recovering. I am even afraid of saying this because I don't want to go down again, so I am not singing victory at all; but come on, if I feel so much better I hope others can feel the same. For first time <b>I am not feeling like I am exploding inside</b>. I am surprised to find I am kind of "normal"...??? I've been doing this treatment for just two or three months no more but I am different from last year for sure! </li>
<li>Ivermectin <b>is a poison to the bugs</b> so it is for us too, so we have to be careful to not ingest poisonous dosages. Better little or small or few drops. Do not get the veterinary medicine unless you know how to do the conversion to human dosages. The little bottles for human are produced at a 6% concentration.</li>
<li>Dr. Q. told me to keep on the Flagyl but stop the Bactrim while on Ivermectin and he said the treatment should be made for a minimum of three months and to even more than one year. He said Ivermectin it is proven not to hurt in long term treatments. He said they first used "Albendazole" but found it could hurt the Central Nervous system, and studies revealed Ivermectin doesn't do this damage!</li>
<li>I am seeing that now I need to go back to antibiotics to fight again the bacteria, now she cannot hide behind the big bugs. I guess they co-exist really good: bacteria feeds from parasites left overs? or viceversa, but they create an environment for subsisting out from a host and help one another, so we need to kill one by one, then kill two at the same time; or mix and combine treatments... </li>
<li>One thing I have learned for sure: what ever bugs these are their lives are cyclic so we need to combat them from time to time in different periods with various types of medicines so they won't adapt or create resistance. </li>
<li>Ivermectin is a new option but also Tindamax - Tinidazole-, Bactrim, Flagyl, Albendazole and many others that kill bugs; plus all the famous ones: Doxy, amoxicillin, Zythro, Ceftin, Cipro, Factive, Malarone or Mepron and etc, so many medicines that are there to try to see if they help.</li>
</ul><ul><li>NO THERE'S NO MAGICAL CURE, NOR A UNIQUE WAY TO TREAT THIS DISEASE.</li>
</ul><ul><li>If your Doctor seems to be "experimenting" with you it is better than a Doctor that doesn't try to get a better recovery or remission and doesn't believe in changes and even risks. This is an every day changing illness and you need to be in the head winning the every day battle.</li>
<li>I do not recommend the use of any medicine nor treatment because I am not a Doctor, nor I believe in anyone trying to sell me anything they say would cure me; they just want to make their money with my illness. Even proteins, vitamins, or any type of curative treatments.</li>
<li>I just present my experience because it has been good after all! God is big; </li>
</ul>Dr. Q is blessed; Dr. J is an angel of many and my Mother in heaven has been every second there for me guiding me; I hear her pushing me to stand up and research and never let me surrender. My Mom read medicine as her passion and her hobby, how could I not try to help my self after being ignored and mistreated by so many Doctors?<br />
<ul><li> I also thank with my sould and "my hurt heart" to my family in Colombia who has sent me so many medicines, finding the way to make them pass without being detected. I'm sure sending bad drugs is easier than sending Amoxicillin, or Cipro, wanna bet? </li>
<li>My beloved husband and daughter and my brother and sister have been part of my recovery, of my every day suffering, of my new hopes and my suriving; without them this journey would have been terribly painful and impossible.</li>
<li>But I'm happy because I've learned to fight and that is more important than just being treated in a blind way by a super Doctor. I believe in trying and researching and mutual help, and new ideas, and traditional medicine, and alternative, and everything that flies is an angel, so what? </li>
<li>I have learned to trust my body and that has been crucial in my recovery. I had a time where I felt the need of eating pineapple... lol... then I discovered this fruit is used to de-worm children... I have been eating "papaya", which I never ate nor even when I lived in South America... well, it helps to clean the gut! LOL! I'm killing the bugs, and cleaning the house in such a "naturalistic" way I never thought I could, my body is telling me how! </li>
<li>Every time I have palpitations I try to know why they are there? I've found some come after taking certain medicines. Some times palpitations are because of the lack of the treatment, like a scheduled medicine not taken and boom palpitations. I learned my heart is talking to me and telling me how good or sick I am. It is not easy and sometimes it has been really difficult but it is a learning process that is not written in any handbook as Dr. J clearly states in his blog of today.</li>
<li>I was so bad I really thought God had really abandoned me... plus all the doctors of the world... I don't think like that anymore. I know this is just another battle in my life and I am going to win it by fighting it and by sharing with who ever needs help or has something to give me too. I have learned to give but also to receive and that is something!</li>
<li>Please read Dr. J's blog, he is very knowledgeable and he might really help you, medically and scientifically talking<span style="font-size: small;">! He now "promotes" Tindamax and Bactrim; before he didn't do it based on IDSA but now his experience has shown him that bugs are killed with these amazing medicines! Read and learn: Sunday, February 14, 2010<a href="http://lymemd.blogspot.com/2010/01/lyme-2010-brief-update.html"> Lyme 2010: A brief update</a> </span></li>
</ul><h3 class="post-title entry-title"></h3> <b>Note:</b> I read about a guy who killed the bugs by spraying himself with poison for ants; I've heard about the ones that believe that just alternative medicine will help them by swallowing tons of nutrients; or what about just salt and vitamin C? I even tried the silver but just used the nasal spray one; 'course it helps; ha... everything helps when you are so extremely sick! Learn that. Even a hot shower helps, so be aware of what you do or take.<br />
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So yes, sometimes we reach desperation but do not loose the faith, God's help is there. Good Doctors are there; good family and or friends are there; I'm here, LOL! WE'LL WIN!<br />
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You can write me if you have any questions or opinions!!!<br />
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QUE VIVA IVERMECTINA!!!MJhttp://www.blogger.com/profile/16614021020877246061noreply@blogger.com3tag:blogger.com,1999:blog-9207742591307790987.post-23927218622946029702010-03-02T23:59:00.000-08:002013-02-27T23:00:29.278-08:00THE WEIRD WORLD OF ILLNESS<span style="font-size: x-large;">SO SHOCKING TO BE IN THE MIDDLE OF THIS WAR...</span><br />
<span style="font-size: x-large;"><br /></span>
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<ul>
<li><span style="font-size: x-large;">The insurers do not want to pay for the long treatments and are supported by the big Medical Boards who do not want to have the haze of treating complicated patients. So, where are we going?</span></li>
</ul>
<ul>
<li><span style="font-size: x-large;">The Doctors don't know how to treat the illness so they have to dismiss it, like, your problem not mine!</span></li>
</ul>
<ul>
<li><span style="font-size: x-large;">Then giving names to confuse the problem, is it chronic or post Lyme? Or should it be called the neuroinflamatory or the neuroparasitic, or no, better the Tick born disease or the tick born co infection and more diseases or...</span></li>
</ul>
<ul>
<li><span style="font-size: x-large;">Everyone around is trying to cure you, by selling you products for their own profit. Rife machines, hyperbaric chambers, antibiotic protocols, natural protocols, DNA testing, Vitamins at $60 dollars each; the processed milk or the colostrum? The miracle curer or just the <span style="font-size: large;">Vitamin C and </span>salt?</span></li>
<li><span style="font-size: x-large;">Having to pay every Doctor at top charges just to be humiliated, or the ones who dare to treat are so much more expensive - $500 for a consult is crazy - and then having to pay for treatment if lucky, so much for an IV antibiotic or $350 for a bottle of pills requiring months and years of these? Mepron can cost $1,800 the tiny bottle? no insurance of course! </span></li>
<li><span style="font-size: x-large;">Have you seen how many new foundations, charities and organizations have grown in the past months? All receiving tons of money to help Lymies? Do we all Lymies should get our own "non for profit" organization to be able to survive and pay for treatment? Cannot work and cannot get disability...?</span></li>
</ul>
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<li><span style="font-size: x-large;">No one knows what is really going on. If they are not suffering it they do not want to hear about it. </span></li>
</ul>
<ul>
<li><span style="font-size: x-large;"> It is scary, no sense, painful, weird, not very demonstrable, improbable or with verifiability; not common, tests not sensitive enough, not known in your area; not probable to get cured, maybe might be in remission meaning could show up again at any moment; unpredictable, unforeseen<span style="font-size: x-large;">, <span style="background-color: #b45f06;"><b>stealth</b></span>...</span></span></li>
</ul>
<b style="mso-bidi-font-weight: normal;"><span style="background: lime; font-family: "Calibri","sans-serif"; font-size: 20.0pt; line-height: 115%; mso-ansi-language: EN-US; mso-ascii-theme-font: minor-latin; mso-bidi-font-family: "Times New Roman"; mso-bidi-language: AR-SA; mso-bidi-theme-font: minor-bidi; mso-fareast-font-family: Calibri; mso-fareast-language: EN-US; mso-fareast-theme-font: minor-latin; mso-hansi-theme-font: minor-latin; mso-highlight: lime;"></span></b><br />
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<span style="font-size: x-large;">We are the victims, we need help</span><br />
<span style="font-size: x-large;">not these!</span><br />
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<span style="font-size: large;"><b><span style="font-size: x-small;">NOTE: LYME THE ROLLERCOASTER BLOG DOES NOT OFFER, DOESN'T GIVE<span style="font-size: x-small;">, </span> NOR INTENDS TO GIVE ANY MEDICAL ADVISE NOR MEDICAL RECOMMENDATIONS.</span></b></span><span style="font-size: small;"><b> <span style="font-family: "Times New Roman","serif"; font-size: x-small;">THESE ARE JUST MY THOUGHTS, IDEAS, RESEARCH AND EXPERIENCE SHARED.</span></b></span> MJhttp://www.blogger.com/profile/16614021020877246061noreply@blogger.com0tag:blogger.com,1999:blog-9207742591307790987.post-64226136178952011812010-01-26T23:39:00.000-08:002013-02-27T22:14:28.913-08:00LYME SEEMS NOT TO BE A SERIOUS ILLNESS!<span style="font-size: x-large;">This blog is just to express my opinions and thoughts. I'm so tired of fighting ...</span><br />
<span style="font-size: x-large;"><br /></span>
<span style="font-size: x-large;">Last year I tried to study a class in a Community College,</span><br />
<span style="font-size: x-large;">but then I had an "explosion of symptoms" that incapacitated me</span><br />
<span style="font-size: x-large;">to accomplish that simple goal -just went to the first class, could never go back;</span><br />
<span style="font-size: x-large;">then sent messages to the Dean of the Faculty stating I was not feeling fine;</span><br />
<span style="font-size: x-large;">no one answered anything, and then boom, I was out for a year!</span><br />
<span style="font-size: x-large;">Not long ago I filed a petition for a refund of what I paid for that class -$600 very needed dollars. The College denied it saying: "while we were sympathetic to your request ... you did not meet our criteria ... which criteria I ask? "This might include but it is not limited to serious illness that prevents the student from completing the required classes..., etc".</span><br />
<span style="font-size: x-large;"><br /></span>
<span style="font-size: x-large;">I JUST WONDER: LYME DISEASE IS NOT A SERIOUS ILLNESS</span><br />
<span style="font-size: x-large;">AND IS NOT AN EXTRAORDINARY CIRCUMSTANCE BEYOND</span><br />
<span style="font-size: x-large;">ANYONE'S CONTROL?</span><br />
<span style="font-size: x-large;">IF IT IS NOT, WHAT DOES?</span><br />
<span style="font-size: x-large;"><br /></span>
<ul>
<li><span style="font-size: x-large;">These so called constellation of symptoms cannot be ignored any longer;</span></li>
</ul>
<ul>
<li><span style="font-size: x-large;">The pain and suffering is always worse; everyday more people is getting infected;</span></li>
</ul>
<ul>
<li><span style="font-size: x-large;">Hello, is anyone out there?</span></li>
</ul>
<span style="font-size: x-large;"><br /></span>
<span style="font-size: x-large;">Here's my long answer to their denial; ha, I'm even asking them to apologize.</span><br />
<span style="font-size: x-large;">They do not have to do it, I just wanted to place my self in a more respectful place.</span>MJhttp://www.blogger.com/profile/16614021020877246061noreply@blogger.com1tag:blogger.com,1999:blog-9207742591307790987.post-66107371447237360472009-11-17T02:46:00.000-08:002013-02-27T23:02:09.619-08:00LYME, THE MEDICAL - POLITICAL FIGHT OF THE CENTURY<span style="font-size: x-large;"><b style="font-family: inherit;">It won’t resolve fast; it will be slow and painful like Lyme Disease does!</b></span><br />
<span style="font-size: x-large;"><br /></span>
<span style="font-size: x-large;"><b style="font-family: inherit;">The question is why the Medical Board is neglecting the pain and suffering of thousands of people by providing insufficient and inappropriate treatment? </b> <b style="font-family: inherit;">Why these big powerful people in the medical area ignore the calling of Doctors, patients and medical personnel who witness that their guidelines are not effective not only to treat, but to cure Lyme disease? Why they do deny a cure? (OF COURSE THERE IS ONE AND MORE!).</b> <b style="font-family: inherit;"><br />
</b></span><br />
<ul>
<li><span style="font-size: x-large;"><b style="font-family: inherit;">Easy first answer, because if the treatment we want to give you doesn’t work for you ALL, it is not our problem, right? We already accomplished treating! We gave you what we think would help you, but if it didn’t work is because you do not have this disease or because your disease has now turned “CHRONIC” so it is not in our hands to treat it! (The most incredible excuse they have is questioning if chronic LD exists or not, or should be called differently or not? Or if LD really exists or not?).</b><span style="font-family: inherit;"> </span><b style="font-family: inherit;"> </b></span></li>
<li><span style="font-size: x-large;"><b style="font-family: inherit;">“Treatment is most often used to mean a process of modifying or altering something, and depending on context may be used in an unqualified form to refer to any of the following: A type of <a href="http://en.wikipedia.org/wiki/Therapy" title="Therapy">therapy</a> used to remedy a health problem; <a href="http://en.wikipedia.org/wiki/Experiment" title="Experiment">Experimental</a> treatment, the levels of treatment factor(s) (variables controlled by the experimenter) applied.” – Wikipedia.</b> </span></li>
</ul>
<ul>
<li><span style="font-size: x-large;"><b style="font-family: inherit;">So, do the guidelines to treat Lyme disease modify or alter in some way the illness or the sick person? (NO).</b><span style="font-family: inherit;"> </span><b style="font-family: inherit;"> </b></span></li>
<li><span style="font-size: x-large;"><b style="font-family: inherit;">Do the treatments proposed in their guidelines are really a therapy used to remedy Lyme disease? (NO).</b><span style="font-family: inherit;"> </span><b style="font-family: inherit;"> </b></span></li>
<li><span style="font-size: x-large;"><b style="font-family: inherit;">Why experimental treatments are not allowed in any level of possibilities? They even deny every other medicine and therapies but just permit the usage of the two only medicines they propose as the God healers that could even be given in really short period of time. (WHY IF THEY DON’T HEAL?).</b><span style="font-family: inherit;"> </span><b style="font-family: inherit;"> </b></span></li>
<li><span style="font-size: x-large;"><b style="font-family: inherit;">But, why are we, the sick, the Doctors and the medical personnel having to fight a political medical scientific fight in here? This is no sense; this is absurd, unfair and cruel. How much longer they are going to take to accept they had a compromised panel and their judgment was impartial and non scientific? I heard this Doctor from the panel stating that he doesn’t approve any other treatment because he doesn’t’ “see the science in it;” meaning like if there were no sustained cases demonstrating that any other treatments might help the patients to recover. The real problem here is that this Doctor has a short vision, that’s all. He doesn’t want to see anything but what he has to say, to justify his partnership or friendship or relationship with the industry and or insurances? ... (Doctor, GLASSES OR CONTACTS?).</b> </span></li>
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<ul>
<li><span style="font-size: x-large;"><b style="font-family: inherit;">So why we keep fighting this fight, when we have to battle with such terrific infection? </b></span></li>
<li><span style="font-size: x-large;"><b style="font-family: inherit;">Why there’s no rush to stop it’s dissemination over the country and other places? </b></span></li>
<li><span style="font-size: x-large;"><b style="font-family: inherit;">Why there’s this feeling that things are not going to change because this medical system is corrupted and just time and tons of deaths will prove them wrong? </b></span></li>
<li><span style="font-size: x-large;"><b style="font-family: inherit;">Why this abandonment and dismissal? Where are the ethic, and the respect, and our rights?</b><span style="font-family: inherit;"> </span><b style="font-family: inherit;"> </b></span></li>
<li><span style="font-size: x-large;"><b style="font-family: inherit;">So what are we supposed to do by following those guidelines? Take the two or three weeks of “Doxy” or “Rocephin” and then to wait to die in pain, quadriplegic and with dementia? How long do we survive to this obligated unique treatment stated by the medical board before our real death comes; about two or three years? </b></span></li>
<li><span style="font-size: x-large;"><b style="font-family: inherit;">Should we just accept our “fate” and live just sick, immobile and not bothering the medical institutions or insurances with our multiplicity of symptoms, due to, if you don’t know, an infection with multiple bacteria and parasites, and worms and viruses? </b></span></li>
<li><span style="font-size: x-large;"><b style="font-family: inherit;">So they are pushing us to accept to be eaten by bugs inside every cell of our bodies? Maybe get some pain killers on the final way? Easy to cope with these right? </b><span style="font-family: inherit;"> </span></span></li>
<li><span style="font-family: inherit; font-size: x-large;"> </span><span style="font-size: x-large;"><b style="font-family: inherit;">Many of us have tried longer and different types of treatment – in hiding an in secret - and most of us are recovering thanks to NOT FOLLOWING these guidelines; you’re “sapient God sent healer guidelines”. </b> <b style="font-family: inherit;"> </b></span></li>
<li><span style="font-size: x-large;"><b style="font-family: inherit;">It is just obvious that a life of a bug is cyclical and has to be attacked several times, or during long periods of time to combat it; more if there are several types of germs, protozoan’s, bacteria and parasites all living inside the same host; meaning inside the same human being suffering it! Come on, how can you contradict this so simple SCIENTIFIC reality? </b></span></li>
<li><span style="font-size: x-large;"><b style="font-family: inherit;">Where’s the ethic and moral, and the swearing to help patients to HEAL. The guidelines are not even offering us a “good decent death”, which is our basic right too, right? where’s the “compassion of the medical field” here?. </b> <b style="font-family: inherit;"> </b></span></li>
<li><span style="font-size: x-large;"><b style="font-family: inherit;">Why they are asking us to survive with a treatment that is PROVEN not to work, not to heal, not to cure, not to remedy the illness? Why they can ask that to us when they won’t be able to take such burden themselves? </b></span></li>
<li><span style="font-size: x-large;"><b style="font-family: inherit;">Why they are using us, experimenting with us when left with a minimum basic treatment, to save money and to gain more? </b></span></li>
<li><span style="font-size: x-large;"><b style="font-family: inherit;"> </b> <b style="font-family: inherit;">For sure they know they have won the battle and they will maybe for as long as they live so they do not have to worry; but I can swear they won’t won the war, because life is fair and will finally tell!</b><span style="font-family: inherit;"> </span></span></li>
<li><span style="font-family: inherit; font-size: x-large;"> </span><span style="font-size: x-large;"><b style="font-family: inherit;">I just know that I prefer to be in my shoes, suffering, than in theirs, so wealthy and healthy, but causing so many to live and die in infinite suffering; at least I can sleep, sometimes! </b> <b style="font-family: inherit;"> </b></span></li>
<li><span style="font-size: x-large;"><b style="font-family: inherit;">Yes it is a not very common illness but very difficult and expensive to treat? Wow, yes, sounds like I am discovering the hot water right? Really new unsaid truth? Unknown?</b><span style="font-family: inherit;"> </span><b style="font-family: inherit;"> </b></span></li>
<li><span style="font-size: x-large;"><b style="font-family: inherit;">And this one: some say it is a hidden illness to not loose tourism; how can something like that be true? It has never been and economical issue, right? never!</b></span></li>
<li><span style="font-size: x-large;"><b style="font-family: inherit;">What if the media says that our cute deers and some little mice have a bug, a tiny tick, that infects humans with a bacteria that the US Medical Board and Governmental Health institutions still cannot kill? And that this tick borne disease produce such severe infection people are physically destroyed cell by cell? </b> <b style="font-family: inherit;">Naa, impossible!</b></span></li>
<li><span style="font-size: x-large;"><b style="font-family: inherit;">I bet they’re waiting for this to propagate to Canada, South America and Europe to blame them and make them invest in the medical research and proper experimentation to find the real cure to LYME DISEASE! It's easier to experiment with people of third countries right?</b></span></li>
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<li><span style="font-size: x-large;"><b style="font-family: inherit;">Mean while they deny, deny and deny; that’s very “political”!</b><span style="font-family: inherit;"> </span><b style="font-family: inherit;"> </b></span><span style="font-size: x-large;"><b style="font-family: inherit;"> </b></span></li>
<li><span style="font-size: x-large;"><b style="font-family: inherit;">If you still have some guts, please watch this video from youtube called<span style="font-size: x-large;">:</span></b></span><span style="font-size: x-large;"><span style="font-size: x-large;"><b> </b></span>"Lyme disease , A cure to late for many", just follow the link:<o:p></o:p></span></li>
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<span style="font-size: x-large;"><o:p>CHEERS! </o:p></span><br />
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<span style="font-size: large;"><b><span style="font-size: x-small;">NOTE: LYME THE ROLLERCOASTER BLOG DOES NOT OFFER, DOESN'T GIVE<span style="font-size: x-small;">, </span> NOR INTENDS TO GIVE ANY MEDICAL ADVISE NOR MEDICAL RECOMMENDATIONS.</span></b></span><span style="font-size: small;"><b> <span style="font-family: "Times New Roman","serif"; font-size: x-small;">THESE ARE JUST MY THOUGHTS, IDEAS, RESEARCH AND EXPERIENCE SHARED.</span></b></span><br />
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<b style="font-family: inherit;"> </b>MJhttp://www.blogger.com/profile/16614021020877246061noreply@blogger.com1tag:blogger.com,1999:blog-9207742591307790987.post-85977206978833781972009-09-26T00:05:00.000-07:002013-02-27T22:15:06.651-08:00LYME, MULTIBACTERIAL POLYPARASITIC INFECTION<span style="font-size: x-large;">I think this title says it all... how can a super small bug, an American tick who is smaller than normal ticks, can transmit such a multiplicity of infections and of so many types of it causing such diversity and large quantity of symptoms all in one same disease? </span><br />
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<li><span style="font-size: x-large;">That information in the guidelines from IDSA stating that their base for treatment of Lyme is two weeks of Doxicicline is very questionable and has been refuted by many scientist, Doctors and patients lately! For me it simply doesn't make too much sense... hey we are talking here about a bacteria that practically "mutates", hides, escapes, transforms, learns to live inside the same white blood cells that are coming to attack her and even then swims freely in the blood... come on, it's devilish and super strong; plus it is not alone. The human host is invaded by an assortment of infections, like if everyone is invited to the party; and I assume that the lack of treatment on time helps the bugs to develop in all stages, nymphs and adults, invading every organ and filling in with co-infections such as other bacteria and parasites and worms...? </span></li>
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<li><span style="font-size: x-large;">Yes, parasites and worms plus a smart, dangerous, terrible bacteria should not be treated with some more care and strength and attention? IDSA says 14 to 21 days of the magic pill and voila, cured; and what ever else that shows up is chronic? please? please!!</span></li>
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<li><span style="font-size: x-large;">But what strongly called my attention from the IDSA "recommendations" is that they DO NOT RECOMMEND ANTI-PARASITARIAN medicines nor BACTERIOSTATIC ONES?? so I do not know how they pretend to kill those bugs; or precisely maybe this is why patients never recover... my humble opinion; my point of view from a sick patients window... and because of the current research, and because of what the logic reason says too... </span></li>
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<li><span style="font-size: x-large;">IDSA literally says in their "journals": <span style="font-style: italic;"><span style="font-weight: bold;">"Therapeutic modalities not recommended. Because of a lack of biologic plausibility, lack of efficacy, absence of supporting data, or the potential for harm to the patient, the following are not recommended for treatment of patients with any manifestation of Lyme disease: first‐generation cephalosporins, fluoroquinolones, carbapenems, vancomycin, metronidazole, tinidazole, amantadine, ketolides, isoniazid, trimethoprim‐sulfamethoxazole, fluconazole, benzathine penicillin G, combinations of antimicrobials, pulsed‐dosing (i.e., dosing on some days but not others), long‐term antibiotic therapy, anti‐Bartonella therapies, hyperbaric oxygen, ozone, fever therapy, intravenous immunoglobulin, cholestyramine, intravenous hydrogen peroxide, specific nutritional supplements, and <strike>others</strike> (see table 4) (E‐III)." </span><span style="font-weight: bold;"> </span></span></span> </li>
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<li><span style="font-size: x-large;">I have tried Bactrim, the trimethopim-sulfa they mention and it has helped me with my swollen and arthritic hands and made my life livable!!! The long term antibiotics therapy and different "protocols" have been made by many Doctors almost in hiding from the CDC and IDSA and they have shown to be more beneficial with outstanding results; but IDSA thinks bugs are dead after the 14th day so patients do not need any further treatments... different thinking ah? The Metronidazole for parasites and all those others including the fluoroquinolones and cephalosporins, even antimalarial and why not veterinarian medicines have deeper penetration in tissues, so denying them, and refusing every other medicine is not leaving any space for other treatment different from their proposed named medicines; and this is a weird marriage IDSA and CDC made... very strange and difficult to understand; not logical nor scientific, nor good for anyone; ... "just this medcine and this one" and nothing else ever; is it ethical?</span></li>
<li><span style="font-size: x-large;">I wonder what do they mean when they say that also "others"- treatments- doesn't work... so nothing? no help from alternative medicine, from homeopathic, from different cultures and possibilities? Why the only accepted treatment is those specific antibiotics and the guideline is so closed to options that have helped some and could help so many others? I would jump in one feet if it helps, anything that might at least mitigate such suffering, can't they relate?</span>
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<li><span style="font-size: x-large;">The worst is, that because of this "simple" guidelines better testing and experiments were never made by the government; the Elisa test has just a sensitivity of 45% - this because they just wanted to say that "everything related to LD was totally under control" - so now, when the illness is propagating all over the country and the world there are no appropriate sensible testing to demonstrate if the bugs are dead or still alive after the treatment with Doxy or the Rocephin or after years of treatment or lack of it, etc. Instead, private enterprises have made <b>studies that reveal not only that the Borrelia is still alive living inside the white blood cells after most of those unique acepted treatments, but also that there are other bugs swimming along the blood stream</b>, some are malaria type, other toxoplasmosis alike, other kind of worms but with bumps in the ends... very scary bugs, weird, unknown and even with no names.... ay Dios mio!</span>
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<li><span style="font-size: x-large;">Just let me share some of what my blood tests read: "Wet mount information result: 1. Numerous small round motile extracellular organisms were observed. Scarce distinctive elongated organisms with bulged ends (dumbbell shapes) were observed..." And I'm "lucky" 'cause I just have these and the Borrelia and Babesia, no more I guess ... other patients have Erlichia, Bartonella, and many more different types of bacteria, parasites and germs all with strange names. -Oh, and read that the IDSA states to <b>not give anti-Bartonella treatments</b>, why? I don't know!-</span></li>
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<li><span style="font-size: x-large;"> So, now what? what treatment, what testing, what insurance help or medical help, what are we supposed to do to survive the multiple bugs and at the same time while walking in one foot - as "Dr. J" says, - fight the injustice of the system, wrestle the ignorance of many Doctors, or their negligence or dismissal to the seriousness of this illness and struggle to get help and to help others hoping our bumpy painful road won't be repeated by anyone else??? Some say it has to be fought in the "political arena", well there might be someone willing to make some money out of this, but us, the sick ones, just can fight from our very presence trying to recover our selves and to be able to share it with others to shorten their road; not much and too much!</span>
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<li><span style="font-size: x-large;">This illness is so extremely painful, it is such a never ending nightmare that <b>we, sick people with Lyme Disease, pray for finding the way to avoid this suffering not even for us, but for the whole world who is endangered of suffering as much as we daily do.</b></span></li>
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<li><span style="font-size: x-large;">I want to add, like my opinion, me being not a scientist, nor a physician nor an expert; just a dummy who pretends to help in the middle of being so hurt; that IDSA and CDC are obligated to hear with an objective position the presentations made in the public hearing, and with those in mind to make changes if not to do total new guidelines to treat and combat and fight this superior disease that might become a horrible pandemic spread from the US to the rest of the world.</span></li>
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<span style="font-size: x-large; font-weight: bold;">People with Lyme Disease needs proper treatment to kill bacteria, parasites, worms and any other type of microorganisms and protozoan, viruses and germs infecting them.</span><span style="font-size: x-large;"> <span style="font-weight: bold;"> </span></span></div>
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<span style="font-size: x-large; font-weight: bold;">Yes IDSA and CDC, as you say Lyme is "not complicated to treat"; you just need to properly detect and kill the bugs, all of them, with accurate medicines and any possible type of treatment that might work, and taking what ever time it takes, and then yes, say it was easy and under control!</span><br />
<span style="font-weight: bold;"><span style="font-size: x-large;">Thank you!</span></span><br />
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<span style="font-weight: bold;"><span style="font-size: x-large;"><span style="font-size: large;"><b><span style="font-size: x-small;">NOTE: LYME THE ROLLERCOASTER BLOG DOES OFFER, GIVES NOR INTENDS TO GIVE ANY MEDICAL ADVISE NOR MEDICAL RECOMMENDATIONS.</span></b></span> </span>
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MJhttp://www.blogger.com/profile/16614021020877246061noreply@blogger.com7tag:blogger.com,1999:blog-9207742591307790987.post-38185934566066665962009-08-20T00:50:00.000-07:002013-02-27T23:05:02.125-08:00LYME, WHAT WORKS!<span style="font-size: large;">Doing something, what ever, always helps; not doing anything is the worst enemy! This one Doctor in the news said, referring to Lyme treatments, that <span style="font-size: x-large;">"</span>sometimes it was better to do nothing" I think he is <span style="font-size: large;">absolutely</span> wrong! This was an excuse for not treating patients with long term antibiotics and for just protecting their backs. A <span id="SPELLING_ERROR_0">Lyme</span> sufferer is so sick that even a bath in hot water is of some help, so come on, do something! So, here's what I think might help alleviate some of the pains and sufferings from Lyme Disease: (And also would mention things that I doubt a little!).First the 'easy" ones, then I'll present the strong stuff!</span><br />
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<li><span style="font-size: large;">Positive attitude. Sounds kind of funny but yes, the illness is so extremely painful and strong that the attitude is vital to be able to take all that and keep on surviving first and recovering later on. Thinking of recovering as a goal really helps. Start with little goals: just to have some minutes feeling fine; then trying to have a good complete hour, and when God provides, to have a good day and why not, to have a glorious day or a whole good week? Just one night, just one movie, just one dinner; enjoy!</span></li>
<li><span style="font-size: large;">Smile. No, not just to have the "positive attitude" but because the facial muscles get so rigid smiling might become an obligated exercise. Other very vital thing of smiling: it moves some tissue/ muscles inside the head that liberates pressure relieving the headache and ear air pressure. If you feel bad smiling because of the Bell's Palsy, smile when you are alone, as a physical therapy, and will also work for the mood and spirit, promise! </span></li>
<li><span style="font-size: large;">Rest and sleep. It is an obligation. The body is weak and this is the only way the body can recover. I read somewhere that the clinical depression is cause by the death of cell's of the brain and the only way to have them recovered was by sleeping. But try to have a regular schedule for sleeping; a Doctor said that the metabolism would recover better if you go back to a normal sleeping schedule.</span></li>
<li><span style="font-size: large;">Silver? have you read about it or have you tried this? Be aware that it is a metal and that it cannot be discharged by the body so easily; and consider that it might be made in proportions that might or not be harmful. But let me say this to honor the reality we <span id="SPELLING_ERROR_1"><span id="SPELLING_ERROR_0">Lymies</span></span> live, if you don't have any other options and are suffering, you have to consider any possibility to help your self, I think... So, I did tried it, but used Silver Sinus <span style="font-weight: bold;">Spray</span>, so I <span style="font-weight: bold;">did not ingest it</span> and just used it to clean inside my nose, and yes it helps for that purpose - like a helper - Some say it could be used instead of antibiotics and it is not accurate because silver might help control a little but cannot kill the bacteria which is a tremendously strong bug! Lyme is very serious and dangerous so it should be treated accordingly!</span></li>
<li><span style="font-size: large;">Iodide? hey, do not mistake the one that can be swallowed with the one used to treat outside skin problems! Iodine is considered a <span id="SPELLING_ERROR_1">bacteriostatic</span> element and it is helpful but should not be taken in amounts that can hurt the thyroid. I have suffered terribly the use of this so called medicine that was given to me without telling me the risks involved. <span id="SPELLING_ERROR_2">LD</span> affects the thyroid by itself, so imagine adding more to the formula? the hyper-<span id="SPELLING_ERROR_3">thyroiditis</span> was brutal! I believe the intention is good because it is about fighting the bacteria, but sometimes little is better; really low dosages might work more without harm! And consider it is "Potassium iodide" the one that can be taken orally, which also means having extra potassium might affect the heart palpitations, right? </span></li>
<li><span id="SPELLING_ERROR_2" style="font-size: large;"><span id="SPELLING_ERROR_4">Cholestyramine</span></span><span style="font-size: large;">? I just read about it and have not tried it yet. Please research about it as an option to get relief of symptoms, seems to be very helpful. This blog talks about it: </span><style>
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<span style="font-size: large;"><a href="http://hopeforlyme.wordpress.com/">http://hopeforlyme.wordpress.com/</a></span> <br />
<li><span style="font-size: large;">Exercise? <span id="SPELLING_ERROR_3"><span id="SPELLING_ERROR_5">Burrascano</span></span> says that the <span id="SPELLING_ERROR_4"><span id="SPELLING_ERROR_6">Borrelia</span></span> is sensitive to heat and oxygen, so a little of exercise seems to be a great help to fight against it. Please read his recommendations <a href="http://www.ilads.org/burrascano_1102.htm#rehab">here! http://www.ilads.org/burrascano_1102.htm#rehab</a> </span>
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<li><span style="font-size: large;">Coffee? oh yeah! "My" Doctor in his blog spoke about the value of drinking coffee when the person is suffering encephalitis, this is brain swelling - obviously lots of headache pain - and let me say, <span id="SPELLING_ERROR_5"><span id="SPELLING_ERROR_7">yesss</span></span> it <span id="SPELLING_ERROR_6"><span id="SPELLING_ERROR_8">workssss</span></span>. It seems like the not healthy thing to do, but sorry when someone is so sick and something little helps, it becomes a miracle. </span></li>
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<li><span style="font-size: large;">Hot baths!! There's a time when the <span id="SPELLING_ERROR_7"><span id="SPELLING_ERROR_9">Lymie</span></span> has heat resistance so the hot bath would be terrible; but when you are all swollen, with pain all over, especially in the back, the hot water seems to be the blessing remedy! Please do not <span id="SPELLING_ERROR_8">exaggerate</span> or you would end burned! Seriously, doesn't need to be so hot, but to be constant temperature and for a while, long time if possible, to help relax the muscles and the mind, believe me! You can take as many baths as you need and want, no limitation in the treatment!</span></li>
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<li><span style="font-size: large;">Information: This is the most important and most vital part of the treatment. Read the blogs, read the protocols, read the books, read the guidelines, watch the videos!</span></li>
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<li><span style="font-size: large;">I do not talk about the "Rife machines" or the "<span id="SPELLING_ERROR_10">Hyperbaric</span> Oxygen therapy" because have no idea if they really work to combat Lyme disease, but i mentioned them here because some think they're helpful. Better research and decide if to try these or not!</span></li>
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<li><span style="font-size: large;">TONIC WATER! funny ah? Well life is curious when you are searching for answers and I found, watching a program of the series of Dr. House, that Tonic Water in the US contains "Quinine," which is known to be the medicine used to kill malaria during 300 years! So, I'm not saying that drinking tonic water with quinine would cure the Lyme, but it is a curious element that might come into the game to reinforce medicines or treatments; please always consult the Doctor to what ever medical decision. Anyways the amount of quinine in tonic water might be very small if not how come people drink gin and other liquor with tonic water this last one containing an antibiotic? weird funny ah?</span></li>
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<li><span style="font-size: large;">Pineapple, fresh and juicy! Yes, I read that it helps with the swelling - recommended to patients with Lupus and of course Lyme 'the inflammatory illness"; and there was a study in Colombia, made by a Doctor I knew for many years, that found that eating pieces of fresh pineapple while fasting, right after you awake and without any other food, would help to get rid of PARASITES! If the sweetness of the pineapple doesn't hurt you, a small piece a day while fasting could help a lot! </span></li>
<span style="font-size: large;">
Now the "strong stuff": <span style="font-weight: bold;">ANTIBIOTICS!</span> Yes, they work and are vital for relieving the symptoms and why not, for a possible recovery or remission of the bacteria (s) and parasite (s)!! And because I am not an expert and cannot give a guide as how to treat with antibiotics I just want to limit my opinion about what I have used, heard or read: </span><ul>
<li><span id="SPELLING_ERROR_9" style="font-size: large;"><span id="SPELLING_ERROR_11">Doxycicline</span></span><span style="font-size: large;">. the famous or infamous <span id="SPELLING_ERROR_10"><span id="SPELLING_ERROR_12">Doxy</span></span> is the number one antibiotic recommended by the <span id="SPELLING_ERROR_11"><span id="SPELLING_ERROR_13">IDSA</span></span> guidelines. Seems to be more effective when it is used IV, and doesn't seem to be so strong when used orally. What I can say is that it is not true that just two weeks of <span id="SPELLING_ERROR_12"><span id="SPELLING_ERROR_14">Doxy</span></span> might cure anything... The bacteria is strong and has cycles that require longer treatments. Also it is not logic or real that taking one or two pills of <span id="SPELLING_ERROR_13"><span id="SPELLING_ERROR_15">Doxy</span></span> after being <span id="SPELLING_ERROR_14">bitten</span> by a tick stops the Lyme for ever... ha, would be really good if true, sorry it is not. To be fair, <span id="SPELLING_ERROR_15"><span id="SPELLING_ERROR_16">Doxy</span></span> has played an important role in the life of the American Lyme, but is is not as famous in other countries, don't know if it is because it is not really good for this or because others don't know her as well!</span></li>
<li><span id="SPELLING_ERROR_16" style="font-size: large;"><span id="SPELLING_ERROR_17">Amoxicillin</span></span><span style="font-size: large;">: This old <span id="SPELLING_ERROR_17">renown</span> antibiotic seems that doesn't work good when left alone, ha, meaning it is being used with other medicines at the same time creating a team that can really try to fight the bug. I have used a not very known medicine called "<span id="SPELLING_ERROR_18"><span id="SPELLING_ERROR_18">Unsayn</span></span>" in the U.S, called "<span id="SPELLING_ERROR_19"><span id="SPELLING_ERROR_19">Sultalbac</span></span>" in South America and <span id="SPELLING_ERROR_20">Trifamox</span> in Europe. It is a combination antibiotic that contains <span id="SPELLING_ERROR_21">Amoxicillin</span> and <span id="SPELLING_ERROR_22">Sultalbac</span>, and I have to report is has been a blessing for me. The <span id="SPELLING_ERROR_23">Unasyn</span> comes only in injections or for IV; the other names are for pills but those are not sold in US. Remember everyone reacts differently and every person requires a special treatment.</span></li>
<li><span id="SPELLING_ERROR_24" style="font-size: large;">Azythromicin</span><span style="font-size: large;">: This one Doctor likes to add it to the treatment as a "joker" that comes and goes when needed. Might be helpful if used as a helper but, my poor opinion, do not treat Lyme with "just" <span id="SPELLING_ERROR_25">Zytro</span>, I think it doesn't really helps and would leave the patient in hands of the bacteria and parasites!!</span></li>
<li><span id="SPELLING_ERROR_26" style="font-size: large;">Biaxin</span><span style="font-size: large;">: seems to be a fighter of first line. But attention, it's a "loner". Better not mix it too much, gives such reactions...the always recommended combination "Biaxin and Plaquenil" seems not to be good now because there is a study now saying that Plaquenil might induce cystic performance of the bacteria! Biaxin seems to be the favorite of my Doctor because it covers a more ample ground attacking the Borrelia and Bartonella and everything around! Might be good with Bactrim too!</span>
</li>
</ul>
<ul>
<li><span id="SPELLING_ERROR_27" style="font-size: large;">Rocephin</span><span style="font-size: large;"> - <span id="SPELLING_ERROR_28">Ceftriaxone</span>; was the very first antibiotic recommended to treat Lyme but it seems to be more helpful when given through IV. The problem is the guidelines IDSA had showed this medication like the one and only miracle cure and during the public hearing one Doctor even said that this medicine was good for nothing! I believe it might be more helpful if accompanied by other antibiotics? Wait, I just found a research made by this Doctor I trust a lot in Colombia, he said Ceftiraxone is "a very good cephalospirin antibiotic with good penetration in tissues IF given in <span style="font-weight: bold;">high</span> doses" ... hello? he said that Rocephin, given in what he calls "sub-doses" or low dosages is not only not helpful but might even be detrimental to the patients. he said that if the regular dose is 500 mg a day they raised it to minimum 1gr and ideally should be at least 1.5 gr; the triple of what has been used!!! </span></li>
<li><span id="SPELLING_ERROR_29" style="font-size: large;">Plaquenil</span><span style="font-size: large;">: <span id="SPELLING_ERROR_30">Hidroxychloroquine</span>, long word! It is a medication used to fight malaria! As big as it sounds it seems to be really good but has to be used for longer periods than the recommended for malaria that "just needs' 3 days, 3 pills to fight the illness of the mosquito, - the down of this medicine is that many say <span id="SPELLING_ERROR_31">Plaquenil</span> as the other anti-malarial are super strong and should not be used for such prolonged periods of time. "My" Doctor said he has treated hundreds of patients with this medicine for longer periods and never had a problem with their vision nor anything. I think it is really useful specially for combating the parasites and bacteria at the same time; plus it is been used for the patients with Lupus. Sorry the information is contradictory now, but it seems that a researcher, Dr. Sapi, found that Plaquenil might induce cyst formation. Hope there's more to say but until today that's all we know!</span>
</li>
</ul>
<ul>
<li><span id="SPELLING_ERROR_32" style="font-size: large;">Bactrim</span><span style="font-size: large;">, blessed! (<span id="SPELLING_ERROR_33">sulfameth</span>/<span id="SPELLING_ERROR_34">Timethoprim</span>). In my condition it has been vital to help me with the swelling. I feel it has cleaned my stomach and made miracles to my hands and even the arthritic pain. But I read a blog where a patient said <span id="SPELLING_ERROR_35">Bactrim</span> didn't help and gave her tremendous bad effects; so, it should be taken with care! I was having the dry mouth symptom so I lowered the dosage of <span id="SPELLING_ERROR_36">Bactrim</span> and my hands started to swell again... What you should know is that <span id="SPELLING_ERROR_37">Bactrim</span> is a sulfa type antibiotic and of course it is really strong and it should be stopped if gives any bad effect or symptom.</span></li>
<li><span id="SPELLING_ERROR_38" style="font-size: large;">Mephon</span><span style="font-size: large;"> and <span id="SPELLING_ERROR_39">Malarone</span>. I present them together because some Doctors seem to replace one for the other like if they are from the same family or generate the same results because both have a common component called "<span id="SPELLING_ERROR_40">Atovaquone</span>". I have not had the experience with any of these, but have to mention them because they seem to be vital in treating Lyme, especially when there are neurological symptoms. For what I have read <span id="SPELLING_ERROR_41">Mepron</span> ends up giving such bad effects that the "medicine is worse than the illness"; but the <span id="SPELLING_ERROR_42">Malarone</span> seems to be more friendly and seems to give better results not only for the <span id="SPELLING_ERROR_43">neuro</span> but against Lyme. "<span id="SPELLING_ERROR_44">MEPRON</span> (<span id="SPELLING_ERROR_45">atovaquone</span>) is an <a href="http://www.rxlist.com/script/main/art.asp?articlekey=10216"><span id="SPELLING_ERROR_46">antiprotozoal</span></a> agent", while <span id="SPELLING_ERROR_47">Malarone</span> is used in the US to treat malaria.</span></li>
<li><span style="font-size: large;">Remember it is not the same to have a bactericidal medicine than a <span id="SPELLING_ERROR_48">bacteriostatic</span>. Let me paste this explanation: "<span id="SPELLING_ERROR_49">Bacteriostatic</span> antibiotics inhibit growth and reproduction of bacteria without killing them; killing is done by <a href="http://en.wikipedia.org/wiki/Bactericide" title="Bactericide">bactericidal</a> agents". "Other bactericidal antibiotics include the <a class="mw-redirect" href="http://en.wikipedia.org/wiki/Fluoroquinolone" title="Fluoroquinolone"><span id="SPELLING_ERROR_50">fluoroquinolones</span></a>, <a href="http://en.wikipedia.org/wiki/Nitrofurantoin" title="Nitrofurantoin"><span id="SPELLING_ERROR_51">nitrofurantoin</span></a>, <a href="http://en.wikipedia.org/wiki/Vancomycin" title="Vancomycin"><span id="SPELLING_ERROR_52">vancomycin</span></a>, <a class="mw-redirect" href="http://en.wikipedia.org/wiki/Monobactam" title="Monobactam"><span id="SPELLING_ERROR_53">monobactams</span></a>, <a href="http://en.wikipedia.org/wiki/Co-trimoxazole" title="Co-trimoxazole">co-<span id="SPELLING_ERROR_54">trimoxazole</span></a>, and <a href="http://en.wikipedia.org/wiki/Metronidazole" title="Metronidazole"><span id="SPELLING_ERROR_55">metronidazole</span></a> - <span id="SPELLING_ERROR_56">Flagyl</span>!-. </span></li>
<li><span style="font-size: large;">So, <span id="SPELLING_ERROR_57">Flagyl</span> or <span id="SPELLING_ERROR_58">metronidazole</span>. The ones that follow "protocols" use the <span id="SPELLING_ERROR_59">Flagyl</span> to "pulse" meaning, they use it every certain periods of time to kill cycles of the bugs. Many say those pulses are really strong and makes them <span id="SPELLING_ERROR_60">herx</span> terribly. I read a blog of someone who proudly announced was doing the "52<span id="SPELLING_ERROR_61">th</span> pulse"? wow! But I have also read from "My" Doctor that this pulses might not be so beneficial because he doesn't believe in short treatments of antibiotics; by the contrary he uses long terms and even low dosages that are risen later on!</span></li>
</ul>
<ul>
<li><span style="font-size: large;"> My thinking, <span style="font-weight: bold;">Bactrim, Flagyl and Ivermectin</span> are soo needed when suffering Lyme Disease because now they are finally finding that we are invaded not only of bacteria but parasites and also WORMS; oh yeah!! </span></li>
<li><span style="font-size: large;">Ivermectin: my new addition! this medicine was originally of veterinary use, but this doctor in Colombia told me they have been using it in patients more than ten years now and found it has a much better penetration to tissues specially with patients who are suffering multiple combination of bacteria and parasites - people that come from rural areas or the jungle; like me from the "jungles of Central Florida... - so they use the Ivermectin one drop per one kilogram of weight once a week during three, six months or even a year depending on the case. He said they used before "Albendazole" but it showed to hurt he Central nervous System and the Ivermectin doesn't. He thinks that if Lyme disease compromises organs due to a variety of bacteria, parasites and worms the treament with Ivermectin should be considered along with antibiotics, and for long time!In the USA the Ivermectin is sold as <span id="main" style="visibility: visible;"><span id="search" style="visibility: visible;">"Stromectol" and it comes in pills, not drops, and the curious thing I've noticed is that they say the treatment is just one unique dose and that's it, cured everything? That's the way it is being used in Europe too so then you hear that patients got well but relapsed later on; it is obvious because bugs have cyclic lives so treatments should be repeated to kill this new born pathogens. I mean it is not logic to treat just once for bugs, it requires several treatments for long periods of time. My thinking!<br />
</span></span></span></li>
</ul>
<ul>
<li><span id="SPELLING_ERROR_62" style="font-size: large;">Cyprofloxacin</span><span style="font-size: large;">: This is deep waters now days! There is a rising group fighting against the use of this type of antibiotics arguing that they damage the tendons and even muscles. There is one guy who has a blog stating that all his bad symptoms are due to the use of <span id="SPELLING_ERROR_63">Fluroquinolones</span>. My experience is that wow, when you have Lyme and take Cipro, you do feel it! The <span id="SPELLING_ERROR_64">Herx</span> is tremendous. I got very heat sensitive and couldn't get near the sun nor even watching it in the <span id="SPELLING_ERROR_65">tv</span>, but I feel it did help me. "My" Doctor says he has not had a patient with ligament rupture in decades of using Cipro, and he is a believer that one of the few antibiotics that is really capable of chasing the bug inside our cells is this one! </span></li>
<li><span id="SPELLING_ERROR_66" style="font-size: large;">Factive</span><span style="font-size: large;"> - <span id="SPELLING_ERROR_67">Gemifloxacin</span> <span id="SPELLING_ERROR_68">Mesylate</span> - other <span id="SPELLING_ERROR_69">fluroquinolone</span>. I read a study where they assure this medicine kills the <span id="SPELLING_ERROR_70">Borrelia</span>. I have no proof nor have read it anywhere else, and will present the link of it here soon; but it gave me hope to think one day we might hear what does really kills the bug, might be this one?</span></li>
<li><span style="font-size: large;">There are so many other antibiotics used for treating <span id="SPELLING_ERROR_71">LD</span>. With God's help I will mention them here later on.</span></li>
</ul>
<span style="font-size: large;">I would like to do a special mention of something curious I found recently, that has been made for centuries to fight bacteria? It is called "<span id="SPELLING_ERROR_72" style="font-weight: bold;">Hemotherapy</span>", it is, injecting one's blood into a muscle to generate a boost in the immune system. It was used to control infections until antibiotics were discovered. I found a video of a Doctor in Brasil who has used hemotherapy as part of his regular treatments to his patients with different diseases and symptoms. It was something he learned from his father and he kept on doing like the traditional way of treating. For us this seems really weird, right? The thing is this Doctor clears that medicine should never "substract" or replace a way of treating if it cures; meaning keep doing the hemotherapy and add the antibiotic therapy as well. This Doctor is not pretentious and didn't know how big the impact of his words could be, but latelly Brazilians found this videos and it was like finding the fountain of the eternal youth so everyone is trying this method, probably because of the lack of medical attention and poverty. I bring this up because it is information we should be aware of and because it might help; my intention is not to tell people to do anything. I think hemotherapy is very interesting and has principles similar to inmunoglobulin and similar to treatments made to stimulate the thymus, just my opinion! Here are the links of the videos with captions in English:
--><a href="http://www.youtube.com/watch?v=t51d6H0TbYI"> http://www.youtube.com/watch?v=t51d6H0TbYI</a> AND <a href="http://www.youtube.com/watch?v=xO4vbB62W_I">http://www.youtube.com/watch?v=xO4vbB62W_I</a></span><style>
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<span style="font-size: large;"> By the moment I would like to add, as my opinion, not as an expert or a Doctor, that Lyme Disease is treatable always, no matter how many days or years of suffering the person or animal has. And it is incredible to see how many people has recovered with long term antibiotics and antiparasitics after being in conditions that seemed impossible to go back. Yes, I said <span style="font-weight: bold;">antibiotics</span>, the other natural products are team mates, but the warriors are the <span id="SPELLING_ERROR_73">bacteriostatics</span> and bactericides and <span id="SPELLING_ERROR_74">parasitarians</span> and <span id="SPELLING_ERROR_75">antimalarians</span> - because the body is invaded by bugs, multibacterial infection with polyparasitic co-infections, right? Have to fight them before they eat you up! God is big! Cheers to getting well! </span><br />
<br />
<span style="font-size: large;"><span style="font-size: large;">I wrote this so long time ago I <span style="font-size: large;">promise</span> to update it with good info soon!!!</span> </span><br />
<br />
<br />
<span style="font-size: large;"><b><span style="font-size: x-small;">NOTE: LYME THE ROLLERCOASTER BLOG DOES NOT OFFER, DOESN'T GIVE<span style="font-size: x-small;">, </span> NOR INTENDS TO GIVE ANY MEDICAL ADVISE NOR MEDICAL RECOMMENDATIONS.</span></b></span><span style="font-size: small;"><b> <span style="font-family: "Times New Roman","serif"; font-size: x-small;">THESE ARE JUST MY THOUGHTS, IDEAS, RESEARCH AND EXPERIENCE SHARED.</span></b></span> MJhttp://www.blogger.com/profile/16614021020877246061noreply@blogger.com0tag:blogger.com,1999:blog-9207742591307790987.post-66100106268814522262009-07-09T02:12:00.000-07:002013-02-27T23:05:25.251-08:00LYME, THE REAL SYMPTOMS!<span style="font-size: large;">It is now being said that Lyme disease is a multi-systemic illness? sounds so huge!
I would like to translate that into more common words based on reality. I do ask you to please excuse me ahead due to words are for sure not enough to describe interminable nights and days of pain, suffering and fear; plus, English is not my first language so I have a limited vocabulary and probably a very particular style in my writing when describing so, sorry for that too.
Let's take a look at each "basic" symptom of Lyme disease. Let's start by a very common one, that seems to be "simple" but is so extremely complex and delicate in reality:
</span><br />
<ol>
<li><span style="font-size: large;"> "Patient presents <span style="color: #6633ff; font-weight: bold;">Neck Stiffness</span>". Who ever reads or hears this could think it is the common stiffness many had felt a couple of times in their lives; but not, the "real" description is far from that: (Nothing that a chiropractor can fix, sorry!)</span></li>
</ol>
<ul>
<li><span style="font-size: large;">the walls of the neck swell up, every gland in the neck swells too and this hurts of course; the sides of the neck become like two hard pillars that impede the head to move and if it does, it really hurts; - like your neck stiffness multiplied by a hundred? - wait, there's more:
</span></li>
<li><span style="font-size: large;">swallowing is painful too, but worse because the trachea feels like loose, and the process of swallowing becomes very difficult, it is slower than usual and it seems that you are going to choke even with your own saliva; - slower swallowing is a problem of the central nervous system, meaning neurological-;
</span></li>
<li><span style="font-size: large;">but the tongue is swollen too so just by being there, by having your tongue inside your mouth - daa- you are kind of choking, no need to drink anything either; - the Chinese Doctors always look at the health of the tongue, swelling means what?
</span></li>
<li><span style="font-size: large;">and due to all this swelling in the neck, the thyroid is not only swollen herself, but also pressed up and hurt by everything around her, so the person gets more symptoms like palpitations, bradycardia (slow rhythm of the heart), arrhythmia (not a regular beat), problems with the hormones, hair loss, dry skin, etc-
</span></li>
<li><span style="font-size: large;">did I mention fear, panic disorders, sleeping problems, depression? just some other symptoms generated by this particular gland called thyroid; and this will have to go to other category because other of the "simple" symptoms Lyme generates is the alteration of all the lymphatic system, meaning the glands of the body, but that's another topic.
</span></li>
<li><span style="font-size: large;">and cannot end talking about the so called "neck stiffness" without also mentioning that this swelling goes deep inside the head, just where the neck gathers with the skull in the back. There's a gland - I think the pituitary - that when swollen causes such a deep pain I call it "The Brutal Pain", and it irradiates to the inside of the head and to the eyes - heat helps a little to relieve it-. Just part of the stiffness... and causes blurry vision and sinus problems...
</span></li>
<li><span style="font-size: large;">The swelling is so huge it might affect the skin of the head too, so the headache is really an encephalitis... painful and dangerous, needs fast attention!
</span></li>
<li><span style="font-size: large;">In my humble opinion, the neck stiffness is an indicator of whether the treatment is working or not. I think the neck stiffness is a result of having the bugs up in the nasal sinuses or maxillary, and the liquid that comes out from the nose or throat it is so contaminated that the body fights it with swelling. I would like to better describe my theory but that is not the point today. I have seen that by treating the sinus with series of antibiotics sometimes many or most of this symptoms go away. Also use salt water to clean sinus passages and everything you might have to help your self!
</span></li>
</ul>
<span style="font-size: large;">2. "<span style="color: #6633ff; font-weight: bold;">Fatigue</span>". If someone comes to me and say I have fatigue, I cannot relate as to truly understand that the person is in such bad condition that can barely move, walk or do any simple activity. </span><br />
<ul>
<li><span style="font-size: large;">The fatigue that affects a Lyme disease patient is not just being a little tired, means the physical body is out of energy to operate;</span></li>
<li><span style="font-size: large;">The fatigue is also having all the muscles loose, like fallen, like not tied to the bones, so the body can hardly move - and it hurts and then it is called "fibromialgya"? just a symptom?</span></li>
<li><span style="font-size: large;">The so called fatigue is also when the bacteria and parasites affected the nervous system, so the response of the muscles and tendons and all the "things" is not as it would be in a healthy situation; the person is not really fatigued, in reality it is not able to do anything!</span></li>
<li><span style="font-size: large;">I would like to add here the symptom called "Generalized malaise" - flu like symptom. It is really a flu but hundred times stronger and lasts forever, simple ah? So I think it should go in the "fatigue" category!</span></li>
<li><span style="font-size: large;">yeah, fatigue seems to be understood as lazy person, not willing... and it is the opposite!
</span></li>
<li><span style="font-size: large;">and in other situations it is precisely one of the symptoms that might easily be considered as an indicator of other illnesses and leads to lots of misdiagnoses...</span></li>
</ul>
<span style="font-size: large;">3. <span style="color: #6633ff; font-weight: bold;">Neurological Symptoms</span>... people think neurological means crazy, or even some Doctors find a neurological symptom and immediately refer the patient to a specialist and or to a psychiatrist... deep water very scary to swim ah?
</span><br />
<ul>
<li><span style="font-size: large;">So let's start mentioning some of these like the so called Bell's Palsy... it is a side of the face that gets kind of paralyzed like the name implies, but it moves when the person talks or eats; it is not that there's no control like when suffering a stroke but the feeling is similar to it, and I bet Lyme sufferers get the "Palsy" precisely due to a "kind of stroke" Lyme Disease "imitates" so well... this symptom is many times a huge indicator of the presence of the bacteria Borrelia... nasty ah? 'cause is not only the suffering, the pain, the having the face numbed like when you go to the dentist, but also the self esteem is affected, sick and ugly ah? - may I say? the long term antibiotic treatment helps to have the face more symmetric-
</span></li>
<li><span style="font-size: large;">some Doctors have learned to "read" into the neurological symptoms to find out and rule in a clinical diagnostic the disease. The tests are not complicated and any Doctor should be able to do them. It is said that the central Nervous system is affected with Lyme Disease, so neurological symptoms might mean Lyme, not just neurological!
</span></li>
<li><span style="font-size: large;">People with Lyme is so hurt that many times don't realize that they have lost sensation in the legs, or down in the toes; many don't know the blurry vision or double vision is a neurological symptom. Some cannot even coordinate touching their nose with one finger and loose many other "simple" skills.</span></li>
<li><span style="font-size: large;">Lyme sufferers might get "inner pains", like inside a leg or inside the hand, and it is purely neurological; plus also have at the same time the muscular pain and the joint pain all together-(as I titled one of my blogs "Lyme, like I've won the lottery", meaning it seems like such a unique astronomic situation! ) So, this inner pains are like a lighting, burning pain; and some cause the fingers or hand to curve, to roll, to be uncontrollably... terrible!</span></li>
<li><span style="font-size: large;">Heat - ha - heat sensations inside the extremities or outside in the skin. Sometimes the feeling is unbearable, other times is just there, constant bothering...</span></li>
<li><span style="font-size: large;">The senses like smell, taste or hearing affected increased or decreased. There's people who suffer of terrible ear pains because they get an increased hearing, and the sounds seem to be so strong the pain becomes unbearable even using ear plugs. It is a real killing pain!
</span></li>
<li><span style="font-size: large;">Other neuro symptoms could be increased smell, and this "simple" symptom affects the taste for the food - so it is loosing the pleasure of eating - and if you add these to the anorexia generated by the parasite babesia well, there's a huge bad situation there involving the vital act of eating.</span></li>
<li><span style="font-size: large;">don't forget the light sensitivity, it's like standing in front of the lights of a huge concert, where you can barely see what's at the other side; and it hurts! I mean, not only unable to see due to the double vision or the blurry one, but because of the light; and not being able to enjoy music because it hurts...
</span></li>
</ul>
<span style="font-size: large;">4. <span style="color: #993399; font-weight: bold;">Arthritis and muscular</span>. (Had to gather these as if they could be easy to explain, but this is getting so long!).
</span><br />
<ul>
<li><span style="font-size: large;">Most of the readings indicate that the person gets a pain in a "large" joint, meaning not all the joints and points to the bigger ones like the knees, well, in my case for example my fingers and wrists have been the ones affected. Maybe because I use them before so much writing? I do not run or make that type of exercise so maybe that's why my knees doesn't hurt? would be good to compare. The point is, the symptom refers to a type of arthritis but tries to show it like a sign not as an illness by itself, differentiated by precisely not affecting all the body, or all the joints but "just" some or even one?</span></li>
<li><span style="font-size: large;">The "Lyme arthritis pain" goes with long antibiotic treatment; I don't know if the arthritis does too? (I am here writing all this thanks to antibiotics if not I will be trying to sleep, writing in my mind, unable to move my fingers for so long!)
</span></li>
<li><span style="font-size: large;">So, just imagine someone with the neurological symptoms and the arthritis ones together singing the same song; and to these please add the muscular pain that also come in a variety of feelings...
</span></li>
<li><span style="font-size: large;">some of the muscular pain, mentioned in the book like just a hurt, is in reality a sharp deep pain that shows out of the blue like cutting the muscle; it's fast and very extremely painful; when you are about to yell it is gone. </span></li>
<li><span style="font-size: large;">The painful sharp pain shows from time to time, and it comes and goes because the person is having treatment and because the person is not having treatment too! (Is this the fibromyalgia that many Doctors refuse to see like muscles affected by bacteria and or parasites?)
</span></li>
<li><span style="font-size: large;">Other is a muscular pain that lasts, that persists and it is there no matter how you move, or if you use hot water or a cold ice... nothing helps! it is a very "stable' constant pain not as strong but yes a seven in a scale of ten.
</span></li>
<li><span style="font-size: large;">This long lasting muscle pain is part of the "fatigue" situation! I believe the long pain is due to having the muscles "loose," meaning that Lyme Disease affects the capacity of the muscle to contract and the muscle structure is lost and the person gets weak, obviously!</span></li>
</ul>
<span style="font-size: large;">5. The <span style="color: #cc33cc; font-weight: bold;">HEART!</span> This special symptom could go with the "muscle division", because it is a muscle, or with the organs affected, but the heart symptom is so particular with Lyme Disease that should be "honored" in a special classification...</span><br />
<ul>
<li><span style="font-size: large;">One of the first, maybe very distinctive symptom of Lyme heart relation is the bradicardia. It is feeling that the heart is beating stronger but slower... is such a weird feeling. People gets scared of having the heart stopped and the "guidelines" recommend to take special care in this cases; well, care given by whom may I ask, because Doctors don't seem to recognize this symptom well. They just send the patient to a Cardiologist who is going to say that the heart is healthy and there's nothing else to do, so the Lyme sufferer will suffer the heart pains and palpitations with no help nor hope!</span></li>
<li><span style="font-size: large;">Oh, well yes, there is something the cardiologist might probably say: "you seem to be very anxious, take these pills for anxiety," ignoring the symptom behind the fear... and who is not anxious feeling the heart is doing funny weird strange painful things?</span></li>
<li><span style="font-size: large;">The heart is being affected directly by the bacteria and by the parasites if this is the case. The heart has to be treated and taken care to avoid damage, don't ask me how.
</span></li>
<li><span style="font-size: large;">Palpitations, fast and sometimes with funny rhythms become part of the every day symptoms of many Lyme sufferers. One thing is to say palpitations and you might relate like when you do exercise and do "cardio" and other thing is to have that speed and strength without moving a finger, or precisely literally because you just moved a finger and those palpitations hurt, hurt badly.</span></li>
<li><span style="font-size: large;">I get palpitations because I have not had the medicine, and the body shows signs of not being fine; but later, because I took the medicine -and it is strong - I also get other type of palpitations. I read something that indicated that the medicines for the malaria were found to be good to regulate the heart palpitations; incredible ah? please do research!
</span></li>
<li><span style="font-size: large;">Other heart symptom with Lyme Disease is a deep pain, inside the chest, deep and sharp but not as strong. It is a pain that lasts, that stays and doesn't let you move because it is very incapacitating. This pain is very confusing because the person cannot tell if it is a sign of a heart attack or not.</span></li>
<li><span style="font-size: large;">And do not forget that the heart, of course is a vital part of the circulatory system, and it is found that Lyme disease, as some times happens with Lupus and other diseases, affects the flow of the blood and the veins - the person feels pains in the veins inside the legs or hands, "just" as part of this multisystemic illness... like if it were not enough with all the other stuff.</span></li>
</ul>
<span style="font-size: large;">Because this writing is so long, and my hands are really tired now, I would like to leave the long list <span style="font-weight: bold;">unfinished</span> and to close saying that what seems to be "just" a group of symptoms is much more than what a "regular illness" might present; and, as you can easily see, it is a very extreme painful situation that requires urgent medical care to help ease so many symptoms popping at the same time. This very sickening illness is not CURED by two weeks of Doxi or in the "worst cases" with four weeks of IV antibiotics; sorry, it requires months and years of a very careful compassionate professional treatment! Ignoring such pain and suffering is obviously negligence!
And let me clear again that these words come from a patient not related to anyone in the industry or medical field or suing someone or anything, just what my suffering had taught me and what I think should be said or made to help others.
</span><br />
<ul style="color: #6600cc; font-weight: bold;">
<li style="color: #3333ff;"><span style="font-size: large;">HEY I DIDN'T MENTION THE RASH AS A SYMPTOM, THE SO CALLED EYE BULL'S RASH? WELL, IT IS A SYMPTOM BUT NOT A UNIQUE INDICATOR BECAUSE MANY TICK BORNE ILL PEOPLE DON'T EVEN HAVE IT, AND WORSE, MANY DOCTORS IGNORE IT!</span></li>
</ul>
<ul style="color: black; font-weight: bold;">
<li><span style="color: #000066; font-size: large;"><span style="color: black; font-weight: normal;">More professionally and better explained symptoms in this place called Lyme disease Foundation, Inc,</span> </span><span style="font-size: large;"><a href="http://www.lyme.org/otherdis/ld_symptoms.html">click here and read!</a></span></li>
</ul>
<span style="font-size: large;">MY GOOD DAYS ARE CALLED <span style="font-weight: bold;">GLORIOUS DAYS</span>; TODAY WAS ONE OF THEM!
THANK YOU GOD!</span><br />
<br />
<span style="font-size: large;"><b><span style="font-size: x-small;">NOTE: LYME THE ROLLERCOASTER BLOG DOES NOT OFFER, DOESN'T GIVE<span style="font-size: x-small;">, </span> NOR INTENDS TO GIVE ANY MEDICAL ADVISE NOR MEDICAL RECOMMENDATIONS.</span></b></span><span style="font-size: small;"><b> <span style="font-family: "Times New Roman","serif"; font-size: x-small;">THESE ARE JUST MY THOUGHTS, IDEAS, RESEARCH AND EXPERIENCE SHARED.</span></b></span> <br />
MJhttp://www.blogger.com/profile/16614021020877246061noreply@blogger.com0tag:blogger.com,1999:blog-9207742591307790987.post-5493792225937000482009-07-08T21:27:00.000-07:002013-02-27T23:06:05.935-08:00FACING DEATH!<span style="color: #3333ff; font-size: large; font-weight: bold;">Someone told me, don't worry this illness is not going to kill you...</span><span style="font-size: large;">
<span style="color: #3333ff; font-weight: bold;">I said, great, good to know, and laughed!</span></span>
<br />
<ul>
<li><span style="font-size: large;">I would like to honor Leslie Wermers, and with her to all the patients who had died of Lyme disease; many feeling abandoned by the medical personnel or by the society who blame them for their illness - "Its all in your head"-.</span></li>
</ul>
<ul>
<li><span style="font-size: large;">I would like to honor Sue Baiata who had to end her life to stop suffering after being neglected by many physicians for years; and with her to many who suffer every day of pain and fear who are not crazy but extremely sick; here we are together gathered in one voice .</span></li>
</ul>
<ul>
<li><span style="font-size: large;">The illness is so strong, and everyday is such a struggle that the Lyme sufferer is facing death every now and then! Yes, everyone is going to die, but who's so strong to live with it's life pending at every second?
</span></li>
</ul>
<ul>
<li><span style="font-size: large;">There are times that the body is so extremely weak that just chocking when swallowing a drink of water might be a deadly situation!
</span></li>
</ul>
<ul>
<li><span style="font-size: large;">Lyme patients suffer "kind of" a heart attack, kind of a stroke, sometimes kind of a paralysis, at the same time might have an arthritis and a cramp that might be muscular or caused by the central nervous system.. yeah, something anyone can handle, not to be worried about right?
</span></li>
</ul>
<ul>
<li><span style="font-size: large;">If Lyme Disease is diagnosed early it might not - not sure - but some say it <span style="font-weight: bold;">might not</span> be a deadly illness, but, how many cases are misdiagnosed versus how many were early diagnosed? IDSA is now offering a Course to medical personnel to teach them how to recognize early symptoms, all based on their guidelines... meaning based on treating with the minimum medicine to get rid of any responsibility...
</span></li>
</ul>
<ul>
<li><span style="font-size: large;">People dies from Lyme Disease but the records say something else like "Heart Failure" or what ever other symptom looks stronger. I think this is unfair because the person was misdiagnosed alive and misdiagnosed dead.
</span></li>
</ul>
<ul>
<li><span style="font-size: large;">Not stating that the person died from Lyme Disease is hiding the truth and the magnitude of the infection.
</span></li>
</ul>
<ul>
<li><span style="font-size: large;">The Public hearing that IDSA organized to see if there's need to review their guidelines, is it going to consider that each patient is facing a death threat every day? ha!
</span></li>
</ul>
<ul>
<li><span style="font-size: large;">Are they (IDSA) going to analyze the magnitude of the problem that now is affecting the public health in the US and threatening the rest of the world?
</span></li>
</ul>
<ul>
<li><span style="font-size: large;">Are they (IDSA) going to change guidelines to help ill people with Lyme Disease who constantly face negligence and are sent to a painful life and death? </span></li>
</ul>
<ul>
<li><span style="font-size: large;">I would also love to be able to thank so many who have dedicated their lives and jobs to help others who are suffering severe illnesses; thank you from our hearts and souls and may God in justice return to you lots of love and care when ever you need it the most.</span></li>
</ul>
<span style="font-size: large;">Please watch the short video of Leslie Wermers -never met her, but she fought for me and I fight for her -; and please read the beautiful article Bob Baiata wrote about her sister Sue.
</span><br />
<ul>
<li><span style="font-size: large;">Leslie's link is here,<a href="http://www.youtube.com/watch?v=NVsfGvZt-LA&eurl=http%3A%2F%2Funderourskin.com%2Fblog%2F%3Fp%3D67&feature=player_embedded"> just click! </a></span></li>
<li><span style="font-size: large;">"My Sister's Batlle with Lyme Disease, John Baiata's article, <a href="http://www.msnbc.msn.com/id/30725967/">click here!</a></span>
</li>
</ul>
<!--[if gte mso 9]><xml> <w:worddocument> <w:view>Normal</w:View> <w:zoom>0</w:Zoom> <w:punctuationkerning/> <w:validateagainstschemas/> <w:saveifxmlinvalid>false</w:SaveIfXMLInvalid> <w:ignoremixedcontent>false</w:IgnoreMixedContent> <w:alwaysshowplaceholdertext>false</w:AlwaysShowPlaceholderText> <w:compatibility> <w:breakwrappedtables/> <w:snaptogridincell/> <w:wraptextwithpunct/> <w:useasianbreakrules/> <w:dontgrowautofit/> </w:Compatibility> <w:browserlevel>MicrosoftInternetExplorer4</w:BrowserLevel> </w:WordDocument> </xml><![endif]--><!--[if gte mso 9]><xml> <w:latentstyles deflockedstate="false" latentstylecount="156"> </w:LatentStyles> </xml><![endif]--><style> <!-- /* Style Definitions */ p.MsoNormal, li.MsoNormal, div.MsoNormal {mso-style-parent:""; margin:0in; margin-bottom:.0001pt; mso-pagination:widow-orphan; font-size:12.0pt; font-family:"Times New Roman"; mso-fareast-font-family:"Times New Roman";} a:link, span.MsoHyperlink {color:blue; text-decoration:underline; text-underline:single;} a:visited, span.MsoHyperlinkFollowed {color:purple; text-decoration:underline; text-underline:single;} @page Section1 {size:8.5in 11.0in; margin:1.0in 1.25in 1.0in 1.25in; mso-header-margin:.5in; mso-footer-margin:.5in; mso-paper-source:0;} div.Section1 {page:Section1;} </style><span style="font-size: large;"> -GRACIAS FOR READING ME! </span><br />
<br />
<span style="font-size: large;"><b><span style="font-size: x-small;">NOTE: LYME THE ROLLERCOASTER BLOG DOES NOT OFFER, DOESN'T GIVE<span style="font-size: x-small;">, </span> NOR INTENDS TO GIVE ANY MEDICAL ADVISE NOR MEDICAL RECOMMENDATIONS.</span></b></span><span style="font-size: small;"><b> <span style="font-family: "Times New Roman","serif"; font-size: x-small;">THESE ARE JUST MY THOUGHTS, IDEAS, RESEARCH AND EXPERIENCE SHARED.</span></b></span> <br />
<!--[if gte mso 9]><xml> <w:worddocument> <w:view>Normal</w:View> <w:zoom>0</w:Zoom> <w:punctuationkerning/> <w:validateagainstschemas/> <w:saveifxmlinvalid>false</w:SaveIfXMLInvalid> <w:ignoremixedcontent>false</w:IgnoreMixedContent> <w:alwaysshowplaceholdertext>false</w:AlwaysShowPlaceholderText> <w:compatibility> <w:breakwrappedtables/> <w:snaptogridincell/> <w:wraptextwithpunct/> <w:useasianbreakrules/> <w:dontgrowautofit/> </w:Compatibility> <w:browserlevel>MicrosoftInternetExplorer4</w:BrowserLevel> </w:WordDocument> </xml><![endif]--><!--[if gte mso 9]><xml> <w:latentstyles deflockedstate="false" latentstylecount="156"> </w:LatentStyles> </xml><![endif]--><style> <!-- /* Style Definitions */ p.MsoNormal, li.MsoNormal, div.MsoNormal {mso-style-parent:""; margin:0in; margin-bottom:.0001pt; mso-pagination:widow-orphan; font-size:12.0pt; font-family:"Times New Roman"; mso-fareast-font-family:"Times New Roman";} @page Section1 {size:8.5in 11.0in; margin:1.0in 1.25in 1.0in 1.25in; mso-header-margin:.5in; mso-footer-margin:.5in; mso-paper-source:0;} div.Section1 {page:Section1;} </style> <!--[if gte mso 10]> <style> /* Style Definitions */ table.MsoNormalTable {mso-style-name:"Table Normal"; mso-tstyle-rowband-size:0; mso-tstyle-colband-size:0; mso-style-noshow:yes; mso-style-parent:""; mso-padding-alt:0in 5.4pt 0in 5.4pt; mso-para-margin:0in; mso-para-margin-bottom:.0001pt; mso-pagination:widow-orphan; font-size:10.0pt; font-family:"Times New Roman"; mso-ansi-language:#0400; mso-fareast-language:#0400; mso-bidi-language:#0400;} </style> <![endif]-->MJhttp://www.blogger.com/profile/16614021020877246061noreply@blogger.com1tag:blogger.com,1999:blog-9207742591307790987.post-34857418922039156712009-06-25T23:03:00.000-07:002009-06-25T23:18:10.416-07:00LYME TREATMENT IS NOT TWO WEEKS!<o:smarttagtype namespaceuri="urn:schemas-microsoft-com:office:smarttags" name="country-region"></o:smarttagtype><o:smarttagtype namespaceuri="urn:schemas-microsoft-com:office:smarttags" name="City"></o:smarttagtype><o:smarttagtype namespaceuri="urn:schemas-microsoft-com:office:smarttags" name="place"></o:smarttagtype><!--[if gte mso 9]><xml> <w:worddocument> <w:view>Normal</w:View> <w:zoom>0</w:Zoom> <w:punctuationkerning/> <w:validateagainstschemas/> <w:saveifxmlinvalid>false</w:SaveIfXMLInvalid> <w:ignoremixedcontent>false</w:IgnoreMixedContent> <w:alwaysshowplaceholdertext>false</w:AlwaysShowPlaceholderText> <w:compatibility> <w:breakwrappedtables/> <w:snaptogridincell/> <w:wraptextwithpunct/> <w:useasianbreakrules/> <w:dontgrowautofit/> </w:Compatibility> <w:browserlevel>MicrosoftInternetExplorer4</w:BrowserLevel> </w:WordDocument> </xml><![endif]--><!--[if gte mso 9]><xml> <w:latentstyles deflockedstate="false" latentstylecount="156"> </w:LatentStyles> </xml><![endif]--><!--[if !mso]><object classid="clsid:38481807-CA0E-42D2-BF39-B33AF135CC4D" id="ieooui"></object> <style> st1\:*{behavior:url(#ieooui) } </style> <![endif]--><style> <!-- /* Font Definitions */ @font-face {font-family:Wingdings; 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mso-level-number-position:left; text-indent:-.25in; mso-ansi-font-size:10.0pt; font-family:Symbol;} ol {margin-bottom:0in;} ul {margin-bottom:0in;} --> </style><!--[if gte mso 10]> <style> /* Style Definitions */ table.MsoNormalTable {mso-style-name:"Table Normal"; mso-tstyle-rowband-size:0; mso-tstyle-colband-size:0; mso-style-noshow:yes; mso-style-parent:""; mso-padding-alt:0in 5.4pt 0in 5.4pt; mso-para-margin:0in; mso-para-margin-bottom:.0001pt; mso-pagination:widow-orphan; font-size:10.0pt; font-family:"Times New Roman"; mso-ansi-language:#0400; mso-fareast-language:#0400; mso-bidi-language:#0400;} </style> <![endif]--> <p class="MsoNormal">GUYS, CAN YOU HEAR ME?
</p><ul><li>JUST WONDER IF THE TREATMENT FOR <b>LYME DISEASE </b>THAT THIS GOVERNMENT AGENCIES PRESENT AS A <b>GUIDELINE</b>, IS <b><span style="color: rgb(153, 0, 0);">PROVEN</span></b> TO <b><span style="color: rgb(204, 0, 0);">CURE</span></b> THE PERSON INFECTED WITH A TICK BORNE DISEASE IN THE <st1:country-region st="on"><st1:place st="on">US</st1:place></st1:country-region>?</li></ul> <ul type="disc"><li class="MsoNormal" style="">I SAID <b>CURE</b>, LIKE MAKE BETTER? LIKE, RECOVERED, GET BACK TO <st1:city st="on"><st1:place st="on">NORMAL</st1:place></st1:city>, HEALED?<o:p></o:p></li></ul> <ul type="disc"><li class="MsoNormal" style="">DOES THAT TREATMENT OF A COUPLE (<b>FEW</b>?) WEEKS OF ANTIBIOTICS -DOXY?- THEY TALK ABOUT AND STRONGLY SUGGEST THE DOCTORS SHOULD FOLLOW, LEAVES THE LYME SUFFERER WITHOUT TRACE OF THE BACTERIA AND OR THE CO-INFECTIONS; OR AT LEAST WITHOUT PAIN AND SYMPTOMS?<o:p></o:p></li></ul> <ul type="disc"><li class="MsoNormal" style="">LIKE WHEN THE <b>MALARIA</b> IS <b>TREATED</b>: A WEEK OF FANSIDAR AND VOILA, THE PERSON IS <b>BACK TO <st1:city st="on"><st1:place st="on">NORMAL</st1:place></st1:city></b>! <b>I HAVE SEEN THAT WITH MY 'BARE' EYES!!!!</b> YOU CAN SEE IT TOO ANYTIME IN AFRICA, <st1:country-region st="on"><st1:place st="on">COLOMBIA</st1:place></st1:country-region>, WHERE EVER YOU WANT! IT'S <b>PROVEN </b>TO WORK, OH YEAH, PROVEN - PROVEN!<o:p></o:p></li></ul> <ul type="disc"><li class="MsoNormal" style="">HAVE YOU SEEN THAT RECOVERY FROM LYME WITH THESE PROPOSED GUIDELINES FOR TREATMENT OF LYME DISEASE? I MEAN, HAVE SOMEONE <b>REALLY SEEN IT</b>? CAN YOU <b>PROVE</b> IT? DOES IT WORKS?<o:p></o:p></li></ul> <ul type="disc"><li class="MsoNormal" style="">SO, THIS RECOMMENDATION TO TREAT LYME WORKS AS ANY OTHER TREATMENT FOR ANY OTHE ILLNESS OR AT LEAST AS <b>ANY OTHER</b> TREATMENT FOR A <b>TICK BORNE DISEASE</b> IN AN ANDEMIC AREA OF THE WORLD?? WHY THE DOUBT AH?<o:p></o:p></li></ul> <ul type="disc"><li class="MsoNormal" style="">I GOT LYME DISEASE SO I JUST NEED TO TAKE A <b>COUPLE OF WEEKS </b>OF DOXYCICLINE AND VOILA, CURED; GO LIVE HAPPILY EVER AFTER? IS THIS WHAT YOU IMPLIED? I'LL BE FINE, OKAY, <st1:city style="font-weight: bold;" st="on"><st1:place st="on">NORMAL</st1:place></st1:city> AGAIN?<o:p></o:p></li></ul> <ul type="disc"><li class="MsoNormal" style=""><b>NO</b>?? WHY NOT? REALITY IS NOT AS YOUR THEORY INDICATES? SO <b>IF I CANNOT GET CURED WITH YOUR GUIDELINES</b>, <b>SO HOW CAN I GET CURED </b>OR PROPERLY TREATED?<b> </b>I HAVE THE <span style="font-weight: bold;">RIGHT</span> TO KNOW! AND THE RIGHT OF BEING ADEQUATELY TREATED TOO!<o:p></o:p></li></ul> <ul type="disc"><li class="MsoNormal" style="">I HOPE YOU ARE NOT PUSHING ME TO GO GET A DOCTOR WHO MIGHT TRY UNUSUAL MEDICATIONS TO <span style="font-weight: bold;">SEE IF LYME CAN GET CURED</span> OR HAVE ME SYMPTOM FREE? YOU ARE THE EXPERTS, <span style="font-weight: bold;">YOU MUST GUIDE ME</span>, US, WE, ALL!<o:p></o:p></li></ul> <ul type="disc"><li class="MsoNormal" style="">WHAT DO YOU MEAN WHEN YOU SAY IF "CATCH ON TIME"? WHEN IS THE <span style="font-weight: bold;">TIME</span> TO CATCH THE ILLNESS AND <span style="font-weight: bold;">TREAT</span> IT? <o:p></o:p></li></ul> <ul type="disc"><li class="MsoNormal" style="">WHY DOCTORS DO NOT RECOGNIZE THE <span style="font-weight: bold;">MULTI- SYMPTOMS A LYME SUFERER</span> HAS? REMEMBER A DOCTOR HAS TO CATCH IT EARLY ON TIME, SO WHY THEY NEVER DO? THEY DENY IT EVEN WHEN SEEING THE BULLS EYE RASH; MAYBE THE <span style="font-weight: bold;">GUIDELINES</span> ARE NOT CLEAR, <span style="font-weight: bold;">NOT COMPLETE</span>, NOT ADEQUATE, NOT ENOUGH?<o:p></o:p></li></ul> <ul type="disc"><li class="MsoNormal" style=""><span style="font-weight: bold;">BORRELIA</span>, BABESIA, BARTONELLA, CHLAMYDIA, ERLICHIA, WEIRD NAMES FOR WEIRD BUGS AND PROTOZOANS CALLED CO-INFECTIONS OF THE TICK BORNE DISEASE, SEEM TO <b>EASILY SURVIVE </b>TO YOUR RECOMMENDED <b>FEW WEEKS</b> OF <b>ANTIBIOTICS</b>; DID YOU KNOW THAT? <o:p></o:p></li></ul> <ul type="disc"><li class="MsoNormal" style="">HOW COME <span style="font-weight: bold;">WE</span>, SIMPLE COMMON PEOPLE, NOT EXPERTS, <span style="font-weight: bold;">KNOW</span> THAT YOUR <span style="font-weight: bold;">GUIDELINES</span> FOR TREATING <span style="font-weight: bold;">LYME</span> DISEASE ARE <span style="font-weight: bold;">NOT COMPLETE</span>, AND YOU <span style="font-weight: bold;">EXPERTS DENY IT</span>?<o:p></o:p></li></ul> <ul type="disc"><li class="MsoNormal" style="">SO EVERY PAIN AND SYMPTOM THAT KEEPS ON GOING <b>AFTER</b> YOUR <b>FEW WEEKS </b>OF TREATMENT IS "<b>CHRONIC</b>", MEANING WHAT, NOT CURABLE? LIVE WITH THAT FOR EVER? WOW, MAY GOD PARDON SUCH NEGLIGENCE!<o:p></o:p></li></ul> <p class="MsoNormal">
CAN THEY <span style="font-weight: bold;">SLEEP</span> AT NIGHT WITH A <span style="font-weight: bold;">CLEAN MIND</span>? I GUESS NOT!</p><p class="MsoNormal">I CAN'T SLEEP OF PAIN, BUT ENJOY MY TIME <b>PRAYING FOR JUSTICE</b>!
</p><ul><li><a href="http://www.cdc.gov/ncidod/dvbid/lyme/">Read them HERE - click!</a></li></ul><p class="MsoNormal">M. J.</p>MJhttp://www.blogger.com/profile/16614021020877246061noreply@blogger.com0tag:blogger.com,1999:blog-9207742591307790987.post-2809615354180302652009-06-23T22:40:00.000-07:002013-02-27T23:18:48.564-08:00LYME DISEASE LINKS AND INFORMATION<span style="font-family: verdana; font-size: large; font-weight: bold;">I hope this information helps to understand the magnitude of Lyme Disease and resources to use.
Just click on the link, but come back to get more!
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<span style="font-size: large;">VIDEOS:</span></div>
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<span style="font-size: large;"><b><span style="font-family: "Times New Roman","serif";">Documentary Film on Lyme Disease and Stealth
Infections</span></b></span></div>
<span style="font-size: large;">
</span><div class="MsoNormal">
<span style="font-size: small;"><a href="https://www.youtube.com/watch?feature=player_embedded&v=Zj9zBXPutvs#">https://www.youtube.com/watch?feature=player_embedded&v=Zj9zBXPutvs#</a>!</span></div>
<br />
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<li><span style="font-size: large;">Good Morning <st1:country-region st="on"><st1:place st="on"><st1:country-region st="on"><st1:place st="on">America</st1:place></st1:country-region></st1:place></st1:country-region>, ABC News <span style="font-size: small;"><a href="http://www.youtube.com/watch?v=zNTm1g-9QgA&feature=related">http://www.youtube.com/watch?v=zNTm1g-9QgA&feature=related</a></span></span></li>
</ul>
<ul style="font-family: verdana; font-weight: bold;">
<li><span style="font-size: large;">CBS News Story About Lyme Disease Epidemic <span style="font-size: small;"> <a href="http://www.youtube.com/watch?v=mSdP-KoaSVk&feature=related">http://www.youtube.com/watch?v=mSdP-KoaSVk&feature=related</a></span></span></li>
</ul>
<ul style="font-family: verdana; font-weight: bold;">
<li><span style="font-size: large;">ABC NEWS - Lyme Disease – MEDICAL MYSTERY<span style="font-size: small;"> </span><span style="font-size: small; font-weight: normal;"><a href="http://www.youtube.com/watch?v=a0sphF174yg&NR=1">http://www.youtube.com/watch?v=a0sphF174yg&NR=1</a></span></span></li>
</ul>
<ul style="font-family: verdana; font-weight: bold;">
<li><span style="font-size: large;">Under Our Skin - Lyme Disease Documentary Trailer <span style="font-size: small;"><a href="http://www.youtube.com/watch?v=sxWgS0XLVqw">http://www.youtube.com/watch?v=sxWgS0XLVqw</a></span></span></li>
</ul>
<ul style="font-family: verdana; font-weight: bold;">
<li><span style="font-size: large;">How the Lyme Disease and treatments work. Publicity of Envita Centers of <st1:country-region st="on"><st1:place st="on"><st1:country-region st="on"><st1:place st="on">America</st1:place></st1:country-region></st1:place></st1:country-region> <span style="font-size: small;"><a href="http://www.youtube.com/watch?v=RTiWfyrNBwA">http://www.youtube.com/watch?v=RTiWfyrNBwA</a></span></span></li>
</ul>
<ul style="font-family: verdana; font-weight: bold;">
<li><span style="font-size: large;">Under Our Skin - Excerpt 2 - The Perfect Storm <span style="font-size: small;"><a href="http://www.youtube.com/watch?v=cwVj_IKP8mY&feature=channel">http://www.youtube.com/watch?v=cwVj_IKP8mY&feature=channel</a></span></span></li>
</ul>
<ul style="font-family: verdana; font-weight: bold;">
<li><span style="font-size: large;">Canadians first to illustrate Lyme disease bacterium <span style="font-size: small;"><a href="http://www.youtube.com/watch?v=635y8E_AiyM&feature=related">http://www.youtube.com/watch?v=635y8E_AiyM&feature=related</a></span></span></li>
</ul>
<ul style="font-family: verdana; font-weight: bold;">
<li><span style="font-size: large;">Under Our Skin - Excerpt 3 - The Price of Misdiagnosis <span style="font-size: small; font-weight: normal;"><a href="http://www.youtube.com/watch?v=W-nJDHVD8QQ&feature=channel">http://www.youtube.com/watch?v=W-nJDHVD8QQ&feature=channe</a></span></span></li>
</ul>
<ul style="font-family: verdana; font-weight: bold;">
<li><span style="font-size: large;">La Enfermedad de Lyme (En espanol) <span style="font-size: small;"><a href="http://www.youtube.com/watch?v=OQ5cN6vuSkU&feature=channel_page">http://www.youtube.com/watch?v=OQ5cN6vuSkU&feature=channel_page</a></span></span></li>
</ul>
<span style="font-family: verdana; font-size: large; font-weight: bold;">BLOGS</span><br />
<ul style="font-family: verdana; font-weight: bold;">
<li><span style="font-size: large;">LYMEMD – DOCTOR IN <st1:city st="on"><st1:city st="on">MONTGOMERY</st1:city></st1:city> <st1:place st="on"><st1:placetype st="on"><st1:place st="on"><st1:placetype st="on">COUNTY</st1:placetype></st1:place> <st1:placename st="on"><st1:placename st="on">MARYLAND</st1:placename></st1:placename></st1:placetype></st1:place> <span style="font-size: small;"><a href="http://lymemd.blogspot.com/">http://lymemd.blogspot.com/</a></span></span></li>
</ul>
<ul style="font-family: verdana; font-weight: bold;">
<li><span style="font-size: large;">LYME BLOG <span style="font-size: small;"><a href="http://lymeblog.com/">http://lymeblog.com/</a></span><u1:p></u1:p></span></li>
</ul>
<ul style="font-family: verdana; font-weight: bold;">
<li><span style="font-size: large;">CPNHELP.ORG Clamydia Pneumonia Blog <span style="font-weight: normal;"> <span style="font-size: small;"><a href="http://www.cpnhelp.org/">http://www.cpnhelp.org/</a></span><u1:p></u1:p></span></span></li>
</ul>
<ul style="font-family: verdana; font-weight: bold;">
<li><span style="font-size: large;">Maria Patricia Juan Blog, “Lyme the Rollercoaster” <a href="http://lymetherollercoaster.blogspot.com/">http://lymetherollercoaster.blogspot.com/</a></span></li>
</ul>
<span style="font-family: verdana; font-size: large; font-weight: bold;"><u1:p></u1:p>
WRITTEN INFORMATION, MEDICAL ARTICLES AND ORGANIZATIONS
</span><br />
<ul style="font-family: verdana; font-weight: bold;">
<li><span style="font-size: large;">Lyme disease From Wikipedia, the free encyclopedia <a href="http://en.wikipedia.org/wiki/Lyme_disease"><span style="font-weight: normal;">http://en.wikipedia.org/wiki/Lyme_disease</span></a></span></li>
<li><span style="font-size: large;"><span style="font-weight: normal;"><span style="font-size: large;">Lyme Disease <span style="font-size: large;">Publisher Brayn Rosner, books and videos: </span></span></span></span></li>
<li><div class="MsoNormal">
<span style="font-size: 18.0pt; line-height: 115%;"><a href="http://www.lymebook.com/">http://www.lymebook.com/</a></span></div>
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<ul style="font-family: verdana; font-weight: bold;">
<li><span style="font-size: large;">Lyme Disease by Fibromyalgia and Fatigue Centers, good article; real. <a href="http://www.fibroandfatigue.com/lymedisease.php?utm_source=adwords&utm_medium=ppc&utm_sponsored=lyme_content&utm_campaign=lyme&gclid=CMn1kYaTopsCFQZeswoduFHgDA">http://www.fibroandfatigue.com/lymedisease.php?utm_source=adwords&utm_medium=ppc&utm_sponsored=lyme_content&utm_campaign=lyme&gclid=CMn1kYaTopsCFQZeswoduFHgDA</a></span></li>
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<li><span style="font-size: large;"><span style="font-weight: normal;">What is Lyme disease? What causes Lyme disease? BY MedicineNet.com <a href="http://www.medicinenet.com/lyme_disease/article.htm">http://www.medicinenet.com/lyme_disease/article.htm</a></span></span></li>
<li><span style="font-size: large;"><span style="font-weight: normal;"><span style="font-size: large;">A great Academy created to help people who cannot find answers to their <span style="font-size: large;">conditions<span style="font-size: large;">: The A<span style="font-size: large;">cademy of Integrative medicine </span></span></span></span></span></span><!--[if gte mso 9]><xml>
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<span style="font-size: 18.0pt; line-height: 115%;"><a href="http://www.acimconnect.com/">http://www.acimconnect.com/</a></span></div>
</li>
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<li><span style="font-size: large;"><span style="font-weight: normal;">CDC – Centers for Disease control and Prevention </span><a href="http://www.cdc.gov/ncidod/dvbid/Lyme/">http://www.cdc.gov/ncidod/dvbid/Lyme/</a></span></li>
</ul>
<ul style="font-family: verdana; font-weight: bold;">
<li><span style="font-size: large;"><span style="font-weight: normal;">IDSA – INFECTIOUS DISEASES OF <st1:country-region st="on"><st1:place st="on"><st1:country-region st="on"><st1:place st="on">AMERICA</st1:place></st1:country-region></st1:place></st1:country-region> </span><a href="http://www.idsociety.org/lymedisease.htm">http://www.idsociety.org/lymedisease.htm</a> </span></li>
</ul>
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<li><span style="font-size: large;"><span style="font-weight: normal;">ILADS – International Lyme and Associated Diseases Society. </span><a href="http://www.ilads.org/basic.html">http://www.ilads.org/basic.html</a></span></li>
</ul>
<span style="font-family: verdana; font-size: large; font-weight: bold;">
LABORATORIES
</span><br />
<ul style="font-family: verdana; font-weight: bold;">
<li><span style="font-size: large;">CLONGEN LABORATORIES </span><!--[if gte mso 9]><xml> <w:worddocument> <w:view>Normal</w:View> <w:zoom>0</w:Zoom> <w:punctuationkerning/> <w:validateagainstschemas/> <w:saveifxmlinvalid>false</w:SaveIfXMLInvalid> <w:ignoremixedcontent>false</w:IgnoreMixedContent> <w:alwaysshowplaceholdertext>false</w:AlwaysShowPlaceholderText> <w:compatibility> <w:breakwrappedtables/> <w:snaptogridincell/> <w:wraptextwithpunct/> <w:useasianbreakrules/> <w:dontgrowautofit/> </w:Compatibility> <w:browserlevel>MicrosoftInternetExplorer4</w:BrowserLevel> </w:WordDocument> </xml><![endif]--><!--[if gte mso 9]><xml> <w:latentstyles deflockedstate="false" latentstylecount="156"> </w:LatentStyles> </xml><![endif]--><style> <!-- /* Style Definitions */ p.MsoNormal, li.MsoNormal, div.MsoNormal {mso-style-parent:""; margin:0in; margin-bottom:.0001pt; mso-pagination:widow-orphan; font-size:12.0pt; font-family:"Times New Roman"; mso-fareast-font-family:"Times New Roman";} h1 {mso-margin-top-alt:auto; margin-right:0in; mso-margin-bottom-alt:auto; margin-left:0in; mso-pagination:widow-orphan; mso-outline-level:1; font-size:24.0pt; font-family:"Times New Roman";} a:link, span.MsoHyperlink {color:blue; text-decoration:underline; text-underline:single;} a:visited, span.MsoHyperlinkFollowed {color:navy; text-decoration:underline; text-underline:single;} @page Section1 {size:8.5in 11.0in; margin:1.0in 1.25in 1.0in 1.25in; mso-header-margin:.5in; mso-footer-margin:.5in; mso-paper-source:0;} div.Section1 {page:Section1;} </style><span style="font-size: large;"><a href="http://www.clongen.com/lyme_disease_testing2.php">http://www.clongen.com/lyme_disease_testing2.php</a></span></li>
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<li><span style="font-size: large;"><span style="font-size: x-large;"><b>Igenex:</b></span></span><b><span style="font-size: 18.0pt; line-height: 115%;"><a href="http://www.igenex.com/Website/"><span style="font-size: x-large;"> </span>http://www.igenex.com/Website/</a></span></b></li>
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<ul style="font-family: verdana; font-weight: bold;">
<li><span style="font-size: large;">Central Florida Research, Inc </span><!--[if gte mso 9]><xml> <w:worddocument> <w:view>Normal</w:View> <w:zoom>0</w:Zoom> <w:punctuationkerning/> <w:validateagainstschemas/> <w:saveifxmlinvalid>false</w:SaveIfXMLInvalid> <w:ignoremixedcontent>false</w:IgnoreMixedContent> <w:alwaysshowplaceholdertext>false</w:AlwaysShowPlaceholderText> <w:compatibility> <w:breakwrappedtables/> <w:snaptogridincell/> <w:wraptextwithpunct/> <w:useasianbreakrules/> <w:dontgrowautofit/> </w:Compatibility> <w:browserlevel>MicrosoftInternetExplorer4</w:BrowserLevel> </w:WordDocument> </xml><![endif]--><!--[if gte mso 9]><xml> <w:latentstyles deflockedstate="false" latentstylecount="156"> </w:LatentStyles> </xml><![endif]--><style> <!-- /* Style Definitions */ p.MsoNormal, li.MsoNormal, div.MsoNormal {mso-style-parent:""; margin:0in; margin-bottom:.0001pt; mso-pagination:widow-orphan; font-size:12.0pt; font-family:"Times New Roman"; mso-fareast-font-family:"Times New Roman";} h1 {mso-margin-top-alt:auto; margin-right:0in; mso-margin-bottom-alt:auto; margin-left:0in; mso-pagination:widow-orphan; mso-outline-level:1; font-size:24.0pt; font-family:"Times New Roman";} a:link, span.MsoHyperlink {color:blue; text-decoration:underline; text-underline:single;} a:visited, span.MsoHyperlinkFollowed {color:navy; text-decoration:underline; text-underline:single;} @page Section1 {size:8.5in 11.0in; margin:1.0in 1.25in 1.0in 1.25in; mso-header-margin:.5in; mso-footer-margin:.5in; mso-paper-source:0;} div.Section1 {page:Section1;} </style><span style="font-size: large;"><a href="http://centralfloridaresearch.com/lab2/">http://centralfloridaresearch.com/lab2/</a> Lyme Antigen Test <a href="http://centralfloridaresearch.com/lab2/index.php?option=com_content&view=article&id=50&Itemid=58"> http://centralfloridaresearch.com/lab2/index.php?option=com_content&view=article&id=50&Itemid=58</a></span></li>
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<span style="font-size: large;"> <span style="font-size: large;">I hope this is a start! ...........</span></span><br />
<span style="font-size: large;"><span style="font-size: large;"><br /></span></span>
<span style="font-size: large;"><span style="font-size: large;"><br /></span></span>
<span style="font-size: x-small;"><b>NOTE: LYME THE ROLLERCOASTER BLOG DOES NOT OFFER, DOESN'T GIVE, NOR INTENDS TO GIVE ANY MEDICAL ADVISE NOR MEDICAL RECOMMENDATIONS.</b><b> <span style="font-family: "Times New Roman","serif";">THESE ARE JUST MY THOUGHTS, IDEAS, RESEARCH AND EXPERIENCE SHARED.</span></b></span> <br />
<span style="font-size: 100%;"><span style="font-size: x-small;"> </span><o:p></o:p>
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</span> <span style="font-family: verdana; font-size: 100%; font-weight: bold;">
</span> <br />
<h1 style="font-family: verdana; font-family: verdana; font-weight: bold; margin-left: 0.75in;">
<span style="font-size: 100%; font-weight: normal;"><o:p> </o:p></span></h1>
<h1 style="margin-left: 0.75in;">
<span style="font-size: 100%;"><a href="http://www.ilads.org/basic.html"></a></span><span style="font-size: 12; font-weight: normal;"><o:p></o:p></span></h1>
<h1 style="margin-left: 0.75in;">
<span style="font-size: 12; font-weight: normal;"><o:p> </o:p></span></h1>
<blockquote>
</blockquote>
MJhttp://www.blogger.com/profile/16614021020877246061noreply@blogger.com0tag:blogger.com,1999:blog-9207742591307790987.post-8318455172562858822009-06-15T23:48:00.000-07:002009-09-27T02:24:40.622-07:00LYME GUIDELINES ARE CRUEL!<!--[if gte mso 10]> <style> /* Style Definitions */ table.MsoNormalTable {mso-style-name:"Table Normal"; mso-tstyle-rowband-size:0; mso-tstyle-colband-size:0; mso-style-noshow:yes; mso-style-priority:99; mso-style-qformat:yes; mso-style-parent:""; mso-padding-alt:0in 5.4pt 0in 5.4pt; mso-para-margin:0in; mso-para-margin-bottom:.0001pt; mso-pagination:widow-orphan; font-size:11.0pt; font-family:"Calibri","sans-serif"; mso-ascii-font-family:Calibri; mso-ascii-theme-font:minor-latin; mso-fareast-font-family:"Times New Roman"; mso-fareast-theme-font:minor-fareast; mso-hansi-font-family:Calibri; mso-hansi-theme-font:minor-latin;} </style> <![endif]--> <!--[if gte mso 9]><xml> <w:worddocument> <w:view>Normal</w:View> <w:zoom>0</w:Zoom> <w:trackmoves/> 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mso-style-parent:""; mso-padding-alt:0in 5.4pt 0in 5.4pt; mso-para-margin:0in; mso-para-margin-bottom:.0001pt; mso-pagination:widow-orphan; font-size:11.0pt; font-family:"Calibri","sans-serif"; mso-ascii-font-family:Calibri; mso-ascii-theme-font:minor-latin; mso-fareast-font-family:"Times New Roman"; mso-fareast-theme-font:minor-fareast; mso-hansi-font-family:Calibri; mso-hansi-theme-font:minor-latin;} </style> <![endif]--> <ul><li><span style="font-size:130%;">It is inexplicable and has no reasonable excuse that "serious" organizations, government oriented say that Lyme disease and its co-infections should be treated with just two, maximum four weeks of antibiotics, like Doxiciline. This is cruel and has no real medical basis. Tick borne infected people need longer and proper treatments to recover a healthy life.</span></li><li><span style="font-size:130%;">How can this so called serious organizations proclaim such treatment (s) knowing that it doesn't kill the bacteria nor the parasites that result from the tick borne infection? Because they do know the bacteria is not killed, murdered, expelled or dead after such short treatments they recommend; or can they dare to say that the bug is completely eradicated and the sufferings of the patient are gone after following their guidelines?<o:p></o:p></span></li><li><span style="font-size:130%;">I dare to make a bet to see if they are right stating that the bacteria is gone, by making lab tests with this laboratory in Central Florida who is now - finally- detecting the bacteria itself, not like the other labs that just detect the reaction of the body to the bacteria.<o:p></o:p></span></li><li><span style="font-size:130%;">You, huge organizations, do you dare to test patients treated, based on your poor guidelines, and then test them to see if they have the bacteria, parasites, protozoans and microorganisms alive? I bet what is left of my health to prove they are still alive and creating colonies inside muscles, tendons, bones, organs, glands and brain of the patients; prove me wrong, please!!!<o:p></o:p></span></li><li><span style="font-size:130%;">So now, after your recommended treatment, because it doesn't really trully completely work, you call "Chronic Lyme" the persisting symtptoms of the patient? "Chronic" meaning, suffering for life and never going to be cured? Is this your excuse after neglecting that the treatment is not complete, is not correct, is not healing?<o:p></o:p></span></li><li><span style="font-size:130%;">Oh, excuse me, now it is not called "chronic" but "Post-Lyme", and it means the same: "suffering for life and never going to be cured?"<o:p></o:p></span></li><li><span style="font-size:130%;">Chronic or post-Lyme, which ever you prefer. Truly meaning negligence in trying harder to find a cure; avoiding spending money in lab tests and medicines at the expense of huge suffering from the tick borne infected people and their families. Even punishing Doctors who have given longer treatments because it cost more money to the insurance; wow, absolute evil!<o:p></o:p></span></li><li><span style="font-size:130%;">Because, if we won't be suffering, if we were there just living like vegetables, you could be there believing that your guidelines are good because they work fine for you and your insurances; but not, you have huge responsibility pending over your heads; every minute we suffer is your accountability!<!--[if gte mso 9]><xml> <u2:worddocument> <u2:view>Normal<u2:zoom>0<u2:trackmoves/> <u2:trackformatting/> <u2:punctuationkerning/> <u2:validateagainstschemas/> <u2:saveifxmlinvalid>false<u2:ignoremixedcontent>false<u2:alwaysshowplaceholdertext>false<u2:donotpromoteqf/> <u2:lidthemeother>EN-US<u2:lidthemeasian>X-NONE<u2:lidthemecomplexscript>X-NONE<u2:compatibility> <u2:breakwrappedtables/> <u2:snaptogridincell/> <u2:wraptextwithpunct/> <u2:useasianbreakrules/> <u2:dontgrowautofit/> <u2:splitpgbreakandparamark/> 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6"> <u4:lsdexception locked="false" priority="71" semihidden="false" unhidewhenused="false" name="Colorful Shading Accent 6"> <u4:lsdexception locked="false" priority="72" semihidden="false" unhidewhenused="false" name="Colorful List Accent 6"> <u4:lsdexception locked="false" priority="73" semihidden="false" unhidewhenused="false" name="Colorful Grid Accent 6"> <u4:lsdexception locked="false" priority="19" semihidden="false" unhidewhenused="false" qformat="true" name="Subtle Emphasis"> <u4:lsdexception locked="false" priority="21" semihidden="false" unhidewhenused="false" qformat="true" name="Intense Emphasis"> <u4:lsdexception locked="false" priority="31" semihidden="false" unhidewhenused="false" qformat="true" name="Subtle Reference"> <u4:lsdexception locked="false" priority="32" semihidden="false" unhidewhenused="false" qformat="true" name="Intense Reference"> <u4:lsdexception locked="false" priority="33" semihidden="false" unhidewhenused="false" qformat="true" name="Book Title"> <u4:lsdexception locked="false" priority="37" name="Bibliography"> <u4:lsdexception locked="false" priority="39" qformat="true" name="TOC Heading"> </u4:lsdexception> </u4:lsdexception> </u4:lsdexception> </u4:lsdexception> </u4:lsdexception> </u4:lsdexception> </u4:lsdexception> </u4:lsdexception> </u4:lsdexception> </u4:lsdexception> </u4:lsdexception> </u4:lsdexception> </u4:lsdexception> </u4:lsdexception> </u4:lsdexception> </u4:lsdexception> </u4:lsdexception> </u4:lsdexception> </u4:lsdexception> </u4:lsdexception> </u4:lsdexception> </u4:lsdexception> </u4:lsdexception> </u4:lsdexception> </u4:lsdexception> </u4:lsdexception> </u4:lsdexception> </u4:lsdexception> </u4:lsdexception> </u4:lsdexception> </u4:lsdexception> </u4:lsdexception> </u4:lsdexception> </u4:lsdexception> </u4:lsdexception> </u4:lsdexception> </u4:lsdexception> </u4:lsdexception> </u4:lsdexception> </u4:lsdexception> </u4:lsdexception> </u4:lsdexception> </u4:lsdexception> </u4:lsdexception> </u4:lsdexception> </u4:lsdexception> </u4:lsdexception> </u4:lsdexception> </u4:lsdexception> </u4:lsdexception> </u4:lsdexception> </u4:lsdexception> </u4:lsdexception> </u4:lsdexception> </u4:lsdexception> </u4:lsdexception> </u4:lsdexception> </u4:lsdexception> </u4:lsdexception> </u4:lsdexception> </u4:lsdexception> </u4:lsdexception> </u4:lsdexception> </u4:lsdexception> </u4:lsdexception> </u4:lsdexception> </u4:lsdexception> </u4:lsdexception> </u4:lsdexception> </u4:lsdexception> </u4:lsdexception> </u4:lsdexception> </u4:lsdexception> </u4:lsdexception> </u4:lsdexception> </u4:lsdexception> </u4:lsdexception> </u4:lsdexception> </u4:lsdexception> </u4:lsdexception> </u4:lsdexception> </u4:lsdexception> </u4:lsdexception> </u4:lsdexception> </u4:lsdexception> </u4:lsdexception> </u4:lsdexception> </u4:lsdexception> </u4:lsdexception> </u4:lsdexception> </u4:lsdexception> </u4:lsdexception> </u4:lsdexception> </u4:lsdexception> </u4:lsdexception> </u4:lsdexception> </u4:lsdexception> </u4:lsdexception> </u4:lsdexception> </u4:lsdexception> </u4:lsdexception> </u4:lsdexception> </u4:lsdexception> </u4:lsdexception> </u4:lsdexception> </u4:lsdexception> </u4:lsdexception> </u4:lsdexception> </u4:lsdexception> </u4:lsdexception> </u4:lsdexception> </u4:lsdexception> </u4:lsdexception> </u4:lsdexception> </u4:lsdexception> </u4:lsdexception> </u4:lsdexception> </u4:lsdexception> </u4:lsdexception> </u4:lsdexception> </u4:lsdexception> </u4:lsdexception> </u4:lsdexception> </u4:lsdexception> </u4:lsdexception> </u4:lsdexception> </u4:lsdexception> </u4:lsdexception> </u4:lsdexception> </u4:lsdexception> </u4:lsdexception> </u4:lsdexception> </u4:lsdexception> </u4:lsdexception> </u4:lsdexception> </u4:lsdexception> </u4:lsdexception> </u4:latentstyles> </xml><![endif]--> <o:p></o:p></span></li><li><span style="font-size:130%;">We are pouring pain every minute you don't treat us properly and the truth will arise and this negligence will be known and the world would judge.<o:p></o:p></span></li><li><span style="font-size:130%;">Some day the medicine will take care of us, long term Lyme sufferers, beyond the limits of your short guidelines! Because at the end, life is always fair!<o:p></o:p></span></li><li><span style=";font-family:arial;font-size:130%;" >I BELIEVE!</span></li></ul>MJhttp://www.blogger.com/profile/16614021020877246061noreply@blogger.com0