Guest guest Posted July 12, 2007 Report Share Posted July 12, 2007 Dagmar- Here is what I posted earlier about MS, which I suffer from. " ILADS has reported that up to 50% of MS, Parkinson's, ALS, etc... are actually misdiagnosed and have aggressive strains of Lyme. The fact that researchers in these different illnesses are currently researching with antibiotics is telling, to me anyway. If you do a google search you should be able to see the Vanderbilt University research with antibiotics and MS. They are having a lot of success with it. There are a group of researchers that believe that MS is a complex infection. Sound familiar? My MS symptoms are almost in remission because of my treatment for Lyme and Mycoplasma infections. It will be interesting to keep up with the MS research and finally get an answer. " They may very well be one in the same or it is just another complex infection. Take care- Torrey LifeLyme of Texas www.lifelyme.org<http://www.lifelyme.org/> PS- s Hopkins is working with a Lyme doc to treat ALS patients with antibiotics. [ ] Re:Lymes question , Welcome. Are you sure you have MS? Lyme is so often misdiagnosed as MS since it has the same symptoms. The only difference is that if you can get the Lyme treated the symptoms of MS go away. I hope you only have Lyme. Sorry about the husband being away. You could really use the support now. We are here to talk, but I suppose that is not the same as having your spouse home. As for the heat looking like rash. Lyme germs can get in your skin close to the surface and literally make you skin thinner. Heat is supposed to kill them there. Try the hottest soaks you can stand and some soothing hypoallergenic lotions. Hope that helps. Take care. Dagmar ************************************** Get a sneak peak of the all-new AOL at http://discover.aol.com/memed/aolcom30tour<http://discover.aol.com/memed/aolcom3\ 0tour> Quote Link to comment Share on other sites More sharing options...
Guest guest Posted April 17, 2008 Report Share Posted April 17, 2008 I was reading the posts about Lyme and Mold. Recently my Lyme IGM is coming up positive, although I had no tick bite (only ever a wasp sting during all these crazy symptoms). My IGG's are all negative. I was just wondering what everyone else's Lyme Western Blot showed. I had 41KD and 23KD positive, but nothing else. What bands did everyone else have positive? I really don't want to take antibiotics again.........took Doxy for about 3 weeks at one point, but the yeast kicks my butt worse than anything becuase I'm so overrun with it anyway from all the treatment attempts. Interesting though how so many have a positive Lyme test that have been exposed to mold. Thanks Quote Link to comment Share on other sites More sharing options...
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