kmilkow...@cfl.rr.com wrote:
They sure do have an awful lot of names for lyme disease, don't they? I think it was Richard?? that put up the origional thread. Might be a good idea to get on the salt/c protocol with a little MMS and some CS mixed in, what do you think?
I'm seriously thinking of lyme. I'm on a fibromyalgia list and a lot of
people there have been found to have chronic lyme after suffering for 20
or more years with typical "fibro" symptoms. I just read a post from a
person on different fibro list who says over 50 list members with
progressively worsening "fibro" symptoms were tested for lyme and found
positive. But the tests are expensive, and often not conclusive, I've
read some lyme tests have 50% false negatives. So I'm thinking of a
trial of salt/C.
If anyone here has done salt/C with success, I'd like to know how long
to see any improvement in symptoms?
sol
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