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Senior Member
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Join Date: Aug 2006
Location: Wild West
Posts: 1,009
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Senior Member
Join Date: Aug 2006
Location: Wild West
Posts: 1,009
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I'm curious about how many with SPMS are or have been on Copaxone (or any of the other DMDs).
I've been on Copaxone nearly 3 years now, and before that I was on Avonex for 3 years. I'm going off Copaxone. It was causing too many problems for me.
I have never been able to find any evidence that Copaxone does much for people with progressive types of MS. And I've been on the lookout.
Oh, and I have 53 like-new Copaxone syringes but I know it's illegal to give them away. I'm just mentioning that I have them. If anyone wants to PM me about them, I'll reply.
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Repeal the law of gravity!
MS diagnosed 1980. Type 2 diabetes, osteoarthritis, osteopenia.
Avonex 2002-2005. Copaxone 6/4/07-5/15/10. Currently: Glatopa (generic Copaxone), 40mg 3 times/week, 12/16/20 - 3/16/24
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