I was diagnosed with FM and MPS while living in TN and was treated well by my doctor there, in fact I felt that I got my life back, was in remission from symptoms and feeling great, I had to move( to MN) and now I cant find doc who believes that Fibro is real, they sent me to a behavior specialist who has continued my Elavil and now has me on Cymbalta instead, but all other meds were taken away, as a result my life was taken away too, I can no longer work or enjoy activities, frustrated and tired of being told my pain is not real...HELP
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