pDoes anyone know of good organizations that are working towards
research and coping What about research that is being done What are
your FM stories No whiners please...I was diagnosed with FM 3 years
ago, and I cant seem to find any activism going on towards finding
reliefcures for this illness...every support group ends up being a
bunch of people who cant stop complaining. I suffer from this
debilitating illness just as much as the next person, but dont want
to complain...I want to hear about success stories, treatments,
people doing something to advance public education and get more
research performed....this illness has progressed quietly long
enough and it is time to get it out there in the public eye, like
AIDS, MS, cancer...even asthma and arthritis have more public
education and understanding. Anyone feel the samep
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