I think this is all very interesting, and really applaud the fact that you would care enough to go to the trouble to help others with a condition you do not have.

But one thing bothers me. What about people like myself who suffer from secondary fibromyalgia? I never had a symptom a day in my life until I developed a chronic pain condition in my abdomen. A year after that the fibromyalgia set in, with all the symptoms, all the tender points and everything.

At that time I did a lot of research myself, and spoke to or e-mailed a number of well-know rheumatologists to try to find a way to treat or cure the fibro despite my chronic pain. The most common answer I got then was that fibromyalgia, at least like mine, is most likely caused by a disruption in the normal cycle of living caused by my chronic pain. I couldn't sleep, eat, work or exercise in any normal pattern, and this caused a huge upset in how my body functioned, leading to FMS.

Do you think there could be more than one cause, or more than one condition that mimics fibromyalgia? From what I've read, it's the tender points more than anything else that confirms the diagnosis, and I have them all. But mine have never been as terribly severe as those of others I've read about here. Any thoughts on that?