Hi NancyCat!
I'm sorry to hear that you haven't been feeling well, although anymore, it seems to be the order of the day! You'll enjoy our "Fibro FAQ" if you haven't already read it.The true "cause" of FMS has yet to be accurately discovered, however, there is a current school of thought about it. Currently, the school of thought is that there is some kind of predisposition (perhaps genetic) to develop FMS, and that a triggering event (such as a viral or bacterial infection, a car accident, etc) then leads to the body developing the disorder.As far as the symptoms of FMS, yes, they definitely wax and wane. It is very much characterized by "flare-ups" that perhaps follow too much physical exertion, mental exertion, or an infection or illness of some sort, etc. It also varies from patient to patient. Some people with FMS live in a constant state of "flare-up", and are rendered disabled by the disorder, while others live fairly normal lives, and are victims of the occasional, annoying "flare-up".The only thing that puzzles me about you is your elevaed white count. That is not characteristic of FMS or CFS. Have you been tested for any auto-immune disorders? (Lupus, Rheumatoid Arthritis, etc) It could even be that you have a number of things going haywire in your body. (hehe, no offense, of course
)At any rate, I hope I've given you some helpful information. The "treating specialist" for FMS is a Rheumatologist. So, you might talk to your GP about getting a referral. In the FAQ, there are links to 3 different websites that can help you find a good physician in your area.Keep us posted on your situation! I hope you can find a good doctor, and start to try to get things sorted. Sometimes, even when there's nothing that can "fix" you, it's at least nice to put a name to the "stuff" you're going through.


