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I'm newly diagnosed with RRMS. I'm rather young and frightened... can anyone give me advice and support? Thanks

Hi all, first time on this site or any forum for that matter. Hope to make freinds and talk to others about ms, the roller coaster ride to diagnosis, and what happens next. Its taken me five years to get diagnosed and treated and ive been knocked back more times than I can remember. hope I can now...

I was diagnosed with RRMS mid May 2020 at the age of 28. All rather shocking because the only symptom I've experienced is optic neuritis. It has been said that I need to start on Tecfidera next week. I'm feeling pretty anxious about this. More so because all my neurologist seems to say is 'No-one ha...

Newly diagnosed with RRMS, worried about what the future holds Struggling to get my head around it

First time posting on here (or anywhere tbh) Newly diagnosed (3 months ish) and was feeling positive and strong but the last couple of weeks sadness and anger has just overwhelmed me. I know I can be positive and I can overcome this but I suppose I’m wondering if you guys had any tips or advise of a...

Feel like I’m in limbo land at the moment which is frustrating. I have an appointment with my neurologist on 20th Sept to discuss my lumbar puncture results, although he’s sent my GP a letter with results and copied me in. MRI showed 4 lesion on my brain Lumbar Puncture confirms “multiple oligoclo...