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!
- Copaxone Information for Consumers
- Copaxone Information for Healthcare Professionals (includes dosage details)
- Side Effects of Copaxone (detailed)
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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 ...
8 answers • 12 Aug 2010
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?
1 answer • 4 Dec 2010
I was dianosed with rrms in 2004 and have had 2 seizures due to meds. Now I am on 200mg topimax,copaxone,150mg effexor and 300mg neurontin, and he ...
1 answer • 15 Mar 2011
... but it seems worse than ever now. Is this normal or connected with copaxone?
2 answers • 7 Jan 2013
- I was hoping to start a local group for support, seeing as i cant really afford counseling and I really see that as the onky way to overcome this ...
1 answer • 8 Apr 2014