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If 1000 people responded to this post, you'd get 1000 different answers. Hits everyone differently. Over my years, I had a flare every year and each year the flare was different. They were very mild like cramping in my hands, or feet or legs, pins and needles in the face. I have developed TN, so thats been around since 2005. My last flare last December hit my legs hard. Couldnt walk, standing was a challenge, very dizzy, legs and feet went numb and I had my first battle with the dreaded "hug". There's more I think, but my memory is also something thats suffering now. My kids get a kick out of talking to me, they say I can say the same thing 5 times but I dont remember. Gotta laugh!!
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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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