This Is MS Multiple Sclerosis Community: Knowledge & Support

**Posted:** Tue Nov 15, 2005 5:37 am

Here's another article about the wonders of Copaxone, submitted by Teva. Once again the study was small and the particpants were "Twenty-two treatment-naïve RRMS patients".

http://www.docguide.com/news/content.ns ... B9005DF226

Dunmann.

**Posted:** Mon Oct 03, 2005 9:05 am

Results from a Copaxone study on children with MS.

http://www.docguide.com/news/content.ns ... 8F0045D5F3

Dunmann.

**Posted:** Mon Oct 03, 2005 7:51 am

An interesting long term study. This is the same post as before... I just wanted to include the text just in case the link went down.

Twenty-Six Year Data With COPAXONE(R) Reinforce Clinical Efficacy and Safety in Relapsing-Remitting Multiple Sclerosis
Monday October 3, 8:00 am ET

Study Represents Extensive, Continuous Clinical Experience With Immune Modulating Therapy

KANSAS CITY, MO--(MARKET WIRE)--Oct 3, 2005 -- Clinical experience and study data with COPAXONE® (glatiramer acetate injection) in relapsing-remitting ...

**Posted:** Wed Sep 28, 2005 6:40 am

**Posted:** Wed Sep 28, 2005 6:39 am

**Posted:** Wed Sep 28, 2005 6:37 am

**Posted:** Mon Sep 12, 2005 8:21 pm

Hey all....IM new to this site......very glad to have found it.

I have a question for you all. Have any of you had a bad bruise than peeling of the skin after using copax? My left arm got it bad....looked like someone hit me...than the skin peeled away leaving a red type scar.

The doctor was stumpped...UGH. It has also happen a little on the right arm....Scared to give the shots in the arms now. ...

**Posted:** Sat Sep 10, 2005 9:49 am

no indents but definite lumps and itching from copaxone injections. set autoinject more shallow per mfg., but still get lumps, although smaller and more spread out, like a large hive. itching seems to be worse. i have been rotating injection sites per instructions and massaging site the next day. help!
linda

**Posted:** Tue Jul 12, 2005 9:06 pm

neuro told me not to ice the injection site before or after - wish he'd mentioned before i started looking like moon crater girl ! 8O

**Posted:** Sat Jun 25, 2005 7:40 am

I recently found out that I am not having the best results from copaxone. I am allergic to the interferons and can not take them. My neuro suggest a course of solumedrol every four months in conjunction to copaxone. Has anyone tried this? If so, how were the results?

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