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Hello! I was diagnosed in 2015, although the first onset was in 2013. Still trying to wrap my head around it all after 5 years! Havent had a full blown relapse since April 16 but have the odd numbness etc. How do you finally come to terms with having this illness and not constantly worry about what ...

Join Roxy, Heather, Maytee, Katt and Dave as they agree and disagree with hot MS topics, opinions and share their multiple sclerosis diagnosis stories. Did you have a difficult diagnosis? Why not share the lessons you learned with the Community in the comments below 👇 https://www.youtube.com/watc...

Hey, just joined this lovely group this week and looking for some contact with others local to me. I’m 51, diagnosed with PPMS- 17 months ago. I’m in Lanarkshire and it would be great to chat, to share ideas, to make some new friends

I am glad to have found this site. I hope I can help someone as they help me. I really need this community.

As an MSer, what would you like to tell your loved ones today? “I still need to talk. Even though I’ve been diagnosed for almost two and a half years…” Our final ‘We Asked 13 MSers’ video is a touching tribute to the support our MSers have, and an appeal for the support they still need. Have you ...