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…

Hello everyone! So I had an episode of CIS in 2016 and then was officially diagnosed in 2018 when I had an MRI for some rather terrible migraines and they found new lesions instead. I haven’t been on treatment yet as the only option was injections and I know I wouldn’t be able to do the…

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…

Hi all, I’m currently on Tecfidera and have just been told I’m eligible for Ocrevus. My MRIs since starting Tec have been mostly stable with a few very small new lesions last year but I don’t love taking the pills every day, often forget them, and then have bad flushing, and my mo…

Hi all. I started on tecfidera 3 weeks ago, the first 2 weeks was fine, no side effects. But this week I am in agony. I have realy bad back pain, neusea, stomach cramps which last for acouple of hours. I have been sent home from work because of this and my 2 year old thinks its a game!!!! My ms nur…

Hi, I am on Tecfidera & have been for nearly 3 years, it’s been good coped well with the slight side effects. My consultant wants me to change to the new drug Ocrelizumab, , which is administered twice a year by drip, taking 3-5 hours. Is anyone else on this drug ? How is it ? Quite nervous t…