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10-12-2013, 01:17 PM
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For all those taking tecfidera (BG-12), How has it affected you? For me, it has slowed me down ALOT! I move slower, my fatigue is worse, dizziness is worse, its like all my symptoms have become worse. I have been on it for only a few months and I want to stop it and see if anthing changes. When I was off it for those 3 weeks to slowly ween back on it, I felt good, and now that Ive been back on it for 2 months I feel horrible. Like Im relapsing. Is anyone else going thru this or anything like this?
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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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