Short Bio |
Was diagnosed witt relapsing-remitting MS back in 1996. I’ve been lucky so far, pretty mild symptoms every few years: mainly tingling, numbness, or paralysis in some random hand or leg muscle. I took Avonex for years and hated it, so finally decided it wasn’t worth it, and took nothing for a bunch of years. For the past 2 /12 years I’ve been receiving an infusion of Rituximab every six months and haven’t had a relapse since then. So far.
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How long have you or the person that you are caring for had MS? |
25 years
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