I hope this is also an MS support group for people using copaxone. Does everyone feel like a pin cushion the way I do?
How do I join the copaxone support group?
- Posted:
- 20 Jul 2012 by Jimfish
- Topics:
- copaxone, multiple sclerosis
Details:
Responses (3)
pledge
jshrier710 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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We have several members on this side also that have MS also. Be patient, & I am sure someone will see your answer. I wish you well... Mary
I have also given you a link about your medication. If you will follow it through to the bottom of the page there are other links listed that will take you to the others links my friend Pledge has spoken of as in the forum. Good luck to you, & have a great weekend...
OOPS! Still early for me! Here is that link! Sorry... Mary
http://www.drugs.com/cdi/copaxone.html
Thanks Mary and I appreciate the link/info. Have a great day my friend