I was diagnosed back in 2004 but just started on Copaxone this month. I was just too scared to start therapy before this. Last Sept I had a BAD relapse......since that time, I have lost most of the feeling in both feet...they just feel numb. I have problems with my vision from time to time, bladder problems that come and go..but it's that burning feeling and numb feeling in my feet that drives me crazy.. I have never regained my feeling back in my feet. I feel like my toes are crossed at times. It's worse when I sit or lay down.
Anyone else experience that? Any one else on Copaxone and how did it work for you?
Anyone else experience that? Any one else on Copaxone and how did it work for you?
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