Why aren't there any groups for myalgic encephalomyelclitis? more and more people are discovering they have m.e. this is directed toward drugs.com. Pheonix rising is a group which is difficult to understand just to ask a question. Why can't an m.e. group be started? Can I start it? or a cfs/me group to learn what works and what doesn't. after all this IS drugs.com and because of mycotoxins which interupted the cycle of my hypothalmus and disturbed my sleep system creating a domino effects of sorts in my brain which my husband and I got from renting a home in OC which had toxic black mold in the master bedroom. (luckily the children were not harmed-that we're aware of. We both suffer daily pain all over our bodies and I have what is worse than cronic fatigue but m.e. which of course is myalgic encephalomyelclitis. Can anyone answer this question for me so we can share information, etc?