Guest guest Posted January 11, 2006 Report Posted January 11, 2006 > I'm beginning to suspect it's time for me to investigate a > mycoplasma infection. But before I go pester my GP about this, I'd > like to have my ducks in a row. My GP doesn't know a lot about > treating ME. While he's happy to work with me, he's even happier > when he knows there's some medical rhyme or reason to my madness. > So I've gotten into the habit of not discussing new initiatives > with him until I can explain what I'm up to, and why. > > A few questions for the group: > > 1) To date, I've not explored this because conventional wisdom said > that ME was a T-2 upregulation issue; and mycoplasmas are addressed > on the T-1 side. However, the fact that so many of us seem to have > mycoplasma infections suggests that this ain't necessarily so. > > I've seen some studies that connect mycoplasma with ME/CFS. Are > there one or more definitive ones I should have in hand when I walk > in the door? I'll have a lot easier time convincing him to pursue > this with me if there's some data suggesting that this is a > medically supportable line of inquiry. > > 2) What are the standard symptoms that would make a doctor (or > patient) suspect mycoplasma infection? > > 3) What standard tests are used to get a positive Dx of mycoplasma? > What results are we looking for on these tests? > > 4) What are the treatment protocols? I'm well aware of Marshall, > thanks -- but moving down to the basement and living like a vampire > for the next two years is not something I'm just thrilled to be > rushing into. On the other hand, I'm extremely intolerant of all > forms of both erythromycin and tetracycline, which are the two > primary drug families used to treat this. So what are the options > here? > > Thanks for your help with this.... > > Sara > > > > Quote
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