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Hi guys, Please can I ask for some direct advice, I am sick of reading government docs etc lol.. anywhere here I go. On copaxone (I have read this is not a risk), relapsed a few months ago, need to return to work so please advise on what is required in the way of a risk assessment?

Hello! I was just wondering if there’s anyone on here that’s started the treatment Tysabri? I’m currently on Copaxone and the neurologist wants me to move over to Tysabri soon. The reason I’m asking is because I’d planned on going travelling next year and am really hoping this new treatment isn’t go...

Hey Guys I hope you are well. I had a question about the medication I’m on. I am 12 weeks pregnant and I am using Copaxone injections. Am I still allowed to inject in my tummy whilst I am pregnant or should I be injecting elsewhere? Thanks

So I had a second relapse this year, this year has been far too much D: so I started my treatment on the 17th August, which is grand, but I have been extremely tired, to the point where I cannot function at all. I have recently finished folic acid, which I was talking for two months, but then starte...

Hello all, So I have been on Copaxone for 3 years. 1st year all good no relapse or new MRI lesions. Second year I got one new lesion but since it was also small my dr said let’s stay on Copaxone. Now my latest MRI showed one new lesion but at the same time I got lipoatrophy on my thigh from the Cop...

I have been feeling so crappy. I am diagnosed with RRMS since 1998 at age of 28. No real problems until 2017! When I had a flare up main symptom dizzy and fatigue - severe. I recovered nearly complete, went on my first dmt copaxone. Annual mris were fine, a couple of small lesions even disappeare...

Just received result of annual MRI of brain and CSP. Quick recap is diagnosed w MS 1998. No DMT or identifiable symptoms until 2017, been on copaxone for 3 years. Most recent MRI says new lesion r fr lobe, and a Highlighting peri ventricular lesion which is also new. I’m feeling a bit alarmed! I ...

Hi i was diagnosed with RRMS in 2012 when i was 26. Now 33 I've tried Copaxone, Gylenya and am on my second year of Mavenclad. With Copaxone i had a relapse and never felt any relief. Also i have permanent divots in my legs and arm because of it. Gylenya I was happy with but still finding symptoms w...

Hi I'm new to this group, I was diagnosed June 2020. My first symptoms started 2hrs ago as Carmel tunnel syndrone. My right arm would go numb for a few minutes and I would shake it off. January 2020 I went to ER with symptoms of right sides numbness and when I bend my forward I feel an electric ting...

Hi everyone! I've found out my MDT are shifting me onto natalizumab, and I want to get people's opinions on how its improved their MS and how you feel about side effects you may get? I know I hate the post injection reactions from copaxone. I've also read that you can take it up to conception, main...