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Junior Member
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I have MS as per 2 very highly regarded neurologists. 1 says start on meds and another says repeat MRI in December and if new lesions then start on meds. I have pain in legs and hands and arms. Tramadol helps. My fatigue is bad. I could never work like this and am awaiting disability determination. The thought of living like this forever is overwhelming. How do you guys go on?
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