my doctor wants me to start dmds, I am rrms. I have just been diagnosed. I have had cramping in my hands to the point they seize and have to be pried open with other hand. Then it’s gone. That was years ago. Then October 2018 numb hands for 6 weeks. Which ended up having me diagnosed. I am back t…

Hi everyone! I was diagnosed a week ago yesterday with RRMS. I’m 29, been married a month and have a 19 month old son. Not the best way to start married life- but I know in life things don’t always go to plan! I guess my question is what happens next? I was sent out the neurologists office wit…

Hi all I was diagnosed with relapsing MS earlier this year. I work as an airline pilot and, as you might expect, was grounded immediately on diagnosis pending further reports. Unfortunately there isn’t much out there about aviation and ms – googling pilot and MS just throws up lots of infor…

Evening all, Looking for reassurance really. I informed the DVLA about my RRMS about 3 months after diagnosis and they have written to me twice since then to let me know that they are still waiting on my consultant to confirm im fit to drive. I dont think it will be an issue as my symptoms have bee…

Hello MS is making loads of people suffer nit just because of the disability and what not But because of the effect of it in other organs I’m not ignoring that But considering the rrms it relapses and fixes itself silently after 2 3 weeks Life goes on literally with rrms as if nothing happens Som…

Hello I was diagnosed with MS in 1998 and have been on Copaxone for about ten years then Rebif and now on Tecfidera for about 5 years or so, I am thinking of changing to Mavenclad which recently got FDA approved in the US. I wanted to know from someone in the UK who tried the drug Mavenclad what th…