Experiences with Copaxone

A board to discuss the Multiple Sclerosis modifying drug Copaxone
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Re: Experiences with Copaxone

Post by TeresaL » Fri Aug 21, 2015 6:50 pm

I have been in copaxone for 7 yrs. was. Dx w RSD at the same time. My rt foot w the RSD is always red, skin dry, flaky, etc. stopped the copaxone 1 month ago..foot looking more normal, skin more normal, etc. I read that it is one of the side effects of copaxon. I have also been on BG-12 for 5 mos plus IVIG for 9 mos. not going back in copaxone

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