Hi everyone,
Has anyone had experience of moving from Gilenya to Mavenclad and if so what did it involve e.g. how long share you taken off Gilenya for etc.
Many thanks in advance for any replies.
I’ve been on Tysabri for the last year and found out I was highly JC virus positive in January. I’ve been advised to switch to another high efficacy DMT in the next year. The top choices I’ve been recommended are Lemtrada and Cladribine. I’d like to know from anyone who has had to make a similar cho...
I had my third infusion of Tysabri today and I’m noticing the side effects getting worse than before. Is anyone else on Tysabri? What are your experiences? I was also curious on when they started to feel the full effects of it. Did it take 6 months to a year until you felt the positive change?
Hi everyone I’m just going through z change of meds moving from Gilenya to Mavenclad providing all my bloods comeback clear. Does anyone have experience of Mavenclad any advice much appreciated
Having a really bad time again at present, significant relapse has knocked me back again, mobility has deteriorated. Been off treatment for two years now, got worse on Ocrevus so that was stopped, tried Kesimpta, had a severe reaction to dose 1, that was stopped, took a while to recover from that. S...
Morning.
Just started my second year of treatment. I’m struggling with side effects of massive headaches, fatigue and nausea.
I’m just wondering what peoples side effects were?
I need some advice in regards to 2 types of medication that’s been prescribed to me to start taking opposite from the previous medication I was taking which was Copaxone. I have been advised to make a decision to take Ocrevus or Kesimpta. I need some advice who can advise me whoever has been taking ...
Hi, everyone I was wondering if anybody has any information on their cladribine - (Mavenclad) experience and any side effects?
What are your experiences/side effects when taking Cladribine(Mavenclad)?
How are your long- ter experience//side effects when finishing the course of treatment?
Than...
Today I am finally starting Mavenclad. After my symptoms started in May 2022 and lesions were found. Finally the medication is starting. I hope it works. However part of me feels it is too late. The pins and needles in my body have started before Christmas.
I'm overthinking.
My first DMD was Rebif 12 years ago... it knocked me around, I stuck with it for a year and the side effects didn't ease.
Four years later I was part of the Tecfidera trial which I was pulled off half way through for the side effects.
For the last 8 years I've been going it al...