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Member
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Join Date: Apr 2012
Location: Indiana
Posts: 430
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Member
Join Date: Apr 2012
Location: Indiana
Posts: 430
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Tecfidera questions..
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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