I have been "majority ruled" diagnosed with FM - after seeing 5 ID's, 2 Rheumies 3 GP's, 2 Neuros, an ENT, and 2 immunologists (!) I am left to do my own research for treatment and ideas as only one of the immunologists offered anything besides tranquilizers and sleeping pills - that being AMP shots (which I have been getting for 6 months). Recently i saw articles on a Parkinsons drug being used for Fibromyalgia, i believe some Fibro docs mention it on their sites as well. My current GP gave me a script for it, but it seems to make me feel WORSE...Anybody have experience with this treatment? Like how long it took to start helping, and did it help?