Mirapex Help Anyone?

Discussion in 'Fibromyalgia Main Forum' started by Enochroot, Mar 6, 2009.

  1. Enochroot

    Enochroot New Member

    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?

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