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I had my first injection of Copaxone on Friday morning and I was unprepared for the stinging that followed which lasted over an hour. I had my second one today and again the stinging was unbearable. Has anyone been on Copaxone injections? Did you have this experience? If so, how did you combat it?...

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

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.....

Hi All I'm just recently had a MS diagnosis 😢. I was with my MS nurse today and considering DMTs. My head is fried! I have been very anti all things medication my whole life and when I read the possible side effects of these meds... my anxiety is through the roof! I have stomach and Gastro issues s...

Hi everyone I’ve been using Copaxone now for nearly 10 years with really good results, but I’m running out of skin to inject because of scar tissue and lose of fat around my stomach. I’ve been diagnosed as secondary progressive now so my MS nurse says I’m not eligible for Oral DMD’S has anyone else...

Hey all. I was recently at my neurologist and she asked whether I would be interested in switching from Copaxone to Ocrevus. I've been on Copaxone since diagnosis and its been working pretty fine for me. I don't really see the need to switch medications. Now I want to hear from yall, is the switch ...

Hello all. I'm thinking this copaxone could be causing more problems than the condition. Would be great to hear others thoughts and comparisons. I'm still fortunately quite mobile, but feel changes happening so not sure what could be a relapse or what could be the medication or Indeed just me overdo...

Hello, Does anybody else have/had HUGE sode effects from the medication copaxone? Really need help

I was diagnosed with relapsing remitting MS 1,5 year ago. The hypothesis of my neurologist was that i had it for at least 10 years before the diagnose because of the numbness, tingling and other symptoms that i was experiencing. They never were severe until 1,5 year ago (when we finally found out th...

Has anyone switched from copaxone to kesimpta how did you go about it and did you think kesimpta helped more than copaxone? X