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So I was dx 2009. Copaxone nearly killed me. Tecfidera caused me severe acne. I lost the feeling from my neck down September last year and finally had an mri in April. I broke my shoulder in October (slipped on holiday in Bulgaria) had surgery there and had plates and pins , they flew me home too ...

Morning all. I was using Copaxone for many years, but stopped around three years ago due to experiencing awful side effects. I used to inject myself in privacy when nobody was at home. One occasion I injected into my right thigh, then experienced what can only be described as a feeling that I was h...

Just spoke to my nurse about my twitching nose. She's booking me for an MRI. On another note!. she was telling me about cases of people taking Copaxone having anaphylactic shocks, even when they've been taking it for a while. Your thoughts.....

Who is here taking copaxone? How does it do for u?

I have had MS for over 28 years and I have been on Betaseron, Copaxone, Avonex, Steroid IV Infusions and I am now on Gilenya. I have a Baclofen pump and a port. If anyone has any questions please feel free to reach out to me. I am all ears and open to helping others cope with their diagnosis of MS.

Hello, I’m not sure how many lesions I have, I had optic neuritis 3 times and then an attack in my feet before I was diagnosed with MS, since I’ve been on treatment I’ve no more attacks, noticeable ones anyway, I was originally on Copaxone, then Techfadera (Which killed my white blood count) and hav...

Diagnosed with MS for 5 years and I’ve been using Copaxone Shots the entire time. I find them easy and very manageable. My NEUROLOGIST after my last MRI would like me to stop shots and change to 4 pills every day. Not excited about this. Anyone else swallowing the 4 pills a day for MS? Side effect...