Roseanna, there are two very helpful lists on the net. They are locate at <http://members.dca.net/menno23/> and <www.ccfa.com>. CCFA is the Crohns Colitis Foundation of America site, the other is a BBS for Crohns and Colitis patients. Both probably will be able to help you with your question. I too have IBD and both sites offer information that has been helpful. Regards, Carlton Edwards ---------- > From: Rmjtracker@aol.com > To: ALDALLAS-L@rootsweb.com > Subject: Re: [ALDALLAS-L] Note fmf and Fibro connection > Date: Sunday, September 12, 1999 7:05 PM > > Dear Nancy: > > Could you please tell me more about FMF and Fibro connection. This isn't idle chit chat. I have Ulcerative Colitis and now have been diag. with FMS and have great trouble sleeping at night. I really need to know if I'm missing something here. I have a lot of muscle pain in various parts of my body and I think, it was by proccess of elimination that the doctors came up with FMS. Although I started going to the doctor about 3 years before I actually stopped working, it didn't stop me from working every day until the last year. > > Perhaps you can tell me something about this or direct me to where I can get additional information. > > Many thanks, Roseanna