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I have read that rrms always eventually becomes spms. Is this so? I have a neuro who says that usually by my age (53 and diagnosed at 29), ms has established the pattern it is going to be. One sounds promising and one not so much. What would clue me in that it’s becoming spms? I have more difficu...

Hi, It’s currently just gone 1am here in the UK after the hottest day this year and I am wrapped up in my duvet and I cannot stop shivering. I’m aware this is a common side effect when using Brabio/Copaxone but was wondering if anyone else has experienced similar and how long does it generally last...

Hi! I am hoping to get some feedback. I am dx RRMS. Doing pretty well, on Glatopa (copaxone) about three years. Anyway, I am having serious joint pain in both hands and mainly thumbs. Maybe carpal tunnel but I have much joint pain in other areas like knees and feet. But the hands are the worst. An...

Hi all, hope everyone is doing well. I just have a question...I've had MS for a few years now, rapidly evolving severe, I've had 2 courses of lemtrada but after 1 year of my last course I had new activity so my neurologist put me on copaxone injections. I wasn't eligible for ocrevus as my immune sys...

Hi, I have rrms, diagnosed in 2010, symptoms since 2007. I started copaxone in 2018, had MRI new lesions. So started tecfidera in February this year. I just wondered as i have not been on dmds for 8 years after being diagnosed. Whether the dmds would be less effective going forward, I know t...

Well, one month on Copaxone and I've had to quit because of the injection site reactions getting too much. It's left dark marks on both hips, my stomach and left a dent in my left thigh after only injecting once. Glad I'm off it. How people could put themselves through that for years I have no idea....

Hi everyone I have had RRMS for 15years and have been relatively well but getting worse recently I'm due to start my copaxone treatment with the first delivery Monday and a nurse coming after that but have now been told it wont be with auto injector and I thought it was supposed to be as my hands sh...

Morning! I was due to start Ocrevus but this has been put on hold due to the current pandemic. I’m currently waiting to commence tysabri instead. Just wondering if anyone else is in the same situation? I had been on Copaxone but the injections were leaving craters all over me and between the burnin...

I am getting a new med for my ms and I am wondering what would be a good one to change from copaxone?

Hi everyone. I have had relapsing remitting ms since 2010, symptoms since 2007. Main symptom numbness from waist down on movement. I have had numbness for 10 plus years. I also get tremors from waist down, usually controlled by medication. I get other sensory issues. I didn't start medication till...