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Just came back from my ms appointment with the neurologist and I'm gonna be starting Tysabri potentially after blood tests? Is this a good medication? As I have no idea what's best treatment. I've looked at some of the potential side effects and worried as I already have some of the issues it says...

Hey everybody. Ocrevus for 2 years and sadly didn't work now spine been really attacked from t11 and lower. Now neurologist has mentioned Tysabri as the next option after the Ocrevus fail. Has anybody experienced Tysabri and if so what can I expect from this treatment?? Thank you all in advance.....

UPDATE: Thank you, everyone, for sharing your experiences. I know everyone is different but it really does help give me a sense of it and what I could experience. Hi everyone. I started my first Tysabri infusion today. The i fusion itself went seamlessly. I was wondering if anyone else was on Tysab...

Hi Folks, just wondering if anyone else is on Tysabri and would like to know is it working for you, any side-affects? I've been on it now for almost 6mths and am thrilled to say I have a lot of my movement back, just feel really tired the week leading up to Infusion. any comments would be appreciate...

Had infusion number five, procedure went ok, but I had issues halfway home driving, It became quite dangerous couldn't get my right leg/foot to work! (Monday) Since then the week has been crap!, headaches,dizziness and my walking has been all over the place ( wobbling ) I was really struggling to dr...

Hi this is my first post. Excuse me if I waffle! I was diagnosed in 2012 with rrms. I've had 3 different dmds. In September I was signed off work for 6 weeks. With what I now think was a stress related relapse. My first real severe relapse. Any way saw my Neuro in October who wants to change me...

Hi just seeing if anyone has switched to the injections of tysabri. I am thinking of doing this just want to find out if any difference and if has the same effect etc? Thanks a mill

Hi Hope everyone having a nice evening, wherever you are. Just wondered if anyone had any words of wisdom on Tysabri? I’ve had all my blood tests, read my information booklet and am now just looking for advice. I’ve looked up tysabri on our site but any more advice or support before making this com...

What are your thoughts on this? I’ve been told I’ll be out on this and next week I’ll be seeing MS nurses about the next step and booking me in for IV’s.

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?