I hope this is also an MS support group for people using copaxone. Does everyone feel like a pin cushion the way I do?
10 Sep 2012
Oh lord! I took copaxon for one year and cried for 1 year! It looked like I had been beat up wherever I took the shot. I was devistated I was going to have to take this shot every day for the rest of my life... Until I was told about Avonex shots which are once a week versus every day. #1. They do not hurt. "Thank God".#2. Once a week. I simply asked my doctor if he would give me Avonex instead of CoPaxon, and he did! Best thing I ever did. I didnt know if I was going to last much longer on CoPaxon and thank the Lord I have Avonex! Please ask your Neurologist! You will not regret it! GOOD LUCK MY FRIEND!
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I am scared to take the chance of it's side effects. I am currently taking copaxone. My condition has gotten slightly worse as far as cognitive ...
Hi there. My sister was diagnosed with MS in Feb. Where can I find a support group in the Gauteng, south of JHB in South Africa?
happened about an hour after injecting Copaxone
... but it seems worse than ever now. Is this normal or connected with copaxone?