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#4 | |||
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Well, Sparky, if you knew nothing about MS, I dont see how its not an appropriate response. I think after the initial shock wears off, and education obtained, reactions change. I really think that if there was more MS awareness out there, all newbies would have a much better reaction. But until that happens, reactions like this, I am afraid, are going to be the norm.
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Dx RRMS April 1992 Yearly flares from 92 to 11 MS induced seizures 2002 Flare Oct 2011 Flare Dec 2011 Left disabled after 2 previous flares Betaseron '02, Copaxone '12, Tecfidera '13 (allergic reaction to all) No longer taking any MS therapy meds |
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