I thought I would throw this out there for all CFS and Fibro patients. You all should consider doing some research on Lyme disease. I believe you all would read Lyme patients stories and feel as though you are looking in the mirror. Please educate yourselves and educate yourself on the controversy of testing.
This is an epidemic and we need to all stick together on raising awareness.
There is a treatment and cure for Lyme, I wish I could say the same for CFS and Fibro. They are both such debilitating illnesses. I lived that story and I can live to tell others how I fought to settle with the diagnosis of MS and CFS!
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