Does 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 can't seem to find any activism going on towards finding relief/cures for this illness...every support group ends up being a bunch of people who can't stop complaining. I suffer from this debilitating illness just as much as the next person, but don't 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 same?
2006-12-14
04:20:12
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5 answers
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asked by
nexgenjenith
2