Are you taking Cladribine for your MS. Turns out it is pretty decent stuff! – Another example of why we need everyone with MS to sign up to the UK MS Register. – https://ukmsregister.org/ – “Over half of MS patients analysed did not relapse or experience disability progressi…

Hi all, I am seriously new to all of this, My RRMS journey has been a whirlwind. I had the MRI and got diagnosed literally overnight. Multiple MS occurences all at once. After a huge course of steriods Methylprednisolone 1000mg 5 days. My flares have calmed down. Not gone away, I my hands are numb …

My neurologist has suggested Ocrelizumab or Mavenclad. He saidBoth are equally effective. Ocrelizumab is 6monthly infusion, while Mavenclad is oral medication-a 2year-course treatment, with 20day-doses over 2year period. Confused? Can I ask members for their experience with either treatments 🤔

@msers Hi all Happy Friday…or whatever day it really is in this COVID19 black hole. Just looking for some info on Mavenclad as am over due starting…hopefully soon-ish… Any issues, tips,advice…affects Am kinda a virgin mser…only officially dx since april 1st this year&#…

@msers Hi all Happy Friday…or whatever day it really is in this COVID19 black hole. Just looking for some info on Mavenclad as am over due starting…hopefully soon-ish… Any issues, tips,advice…affects Am kinda a virgin mser…only officially dx since april 1st this year&#…

Hi 👋 I completed my first round of Mavenclad in February of this year and received my letter from the Government asking me to “Shield” for 12 weeks in March, due to the risk of possible complications from COVID-19. At that time my lymphocytes were 0.8. Does anyone know what lymphocyte level …