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polymyositis or MS?
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An_253731 posted:
was diagnosed with poly at mayo clinic last may. i have all the symptoms of MS only test not performed was a spinal tap. i am on 50 mg. prdnisone and 100 imuran. have beenbruising badly, bleeding (skin) since i have been o iumuran. going to see a neurologist at marshfield wi next month. rheumatologists cant seem to agree on ,line of treatment. can mypositis be mistaken for ms? I KNOW how I feel, what is happenig to me, etc. thanks.... are sponal taps THE best way to diagnose ms? I have had emgs, mris, labs every week. my seds are elevated, cks in the 2500 area, adolase is streaming out of my muscles.... help!
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