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ErikaMo
New Member


Date Joined Nov 2017
Total Posts : 7
   Posted 11/9/2017 2:40 PM (GMT -7)   
Hello all-
I have only recently been diagnosed; treated for my flare up with steroids; and now- onto the full time medication. My doctor and I decided on Copaxone. I believe I will be doing the 3 times per week injections. Can anyone whom has been on this medication give me any input or feedback on it? From my minimal research; side effects seem to be fairly minimal... but everyone is different.

Gretchen1
Forum Moderator


Date Joined Jan 2007
Total Posts : 3546
   Posted 11/10/2017 8:52 PM (GMT -7)   
I've been on copaxone for 11 years. It's been a solid medication for me. I've had very slow to no progression. I've not had an issue with side effects. Just the typical local pain and redness for a few minutes. I hope it works for you!
Diagnosed with MS July 2006, Celiacs 2012, RA January 2017

I have no lesions on my soul and so I live with no limits.
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