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Hi, I have been having the Tysabri infusion since Feb 2020, and today just found out that I’m due to swap from having the 2-3hr infusion (monthly) to the subcutaneous Tysabri jab (monthly) in its place….. plus side is it’s a lot quicker and for the first 6 months I just need to be monitored for a...

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.....

I was a bit nervous about changing from Tysabri infusions to Tysabri sub cut injections . I’ve had my 3 rd one on wed gone . So far so good . Just wondering if anyone is having any negative experiences with Tysabri sub cut . Thanks , Lisa

I was on tysabri injections every 4 weeks but I have now become JC virus positive so they switched me to every 6 weeks I have opted to switch treatment (can't remember the name) but I injections myself it's every month & I no longer have to go to the hospital which is a bonus!! I know I can't rememb...

So, a bit of a backstory on my situation.. I was diagnosed in November 2021 with RRMS. I received my diagnosis after having numbness and tingling in both arms and legs and suffering optic neuritis which pretty much completely took my vision in my left eye. Luckily I got my vision back and it’s just ...

Hi, I’m currently going into my 7th week without my Tysabri infusion (usually 4 weekly soon to be 6 weekly but missed last infusion as had UTI and was on antibiotics so MS team advised I wasn’t allowed it). Does anyone feel that Tysabri increases their energy levels or reduces fatigue? I’m definite...

Hi can anyone tell me is it safe to take cbd oil whilst on tysabri ? Thanks Jenny

Hi! Hope Saturday is being good to you! I moved to my 4 week Tysabri dose to every 6 weeks in August/September 2023... and wondering if anyone else did, and if so, how you're getting on with it? (I felt the 'need' for it in the week running up to infusion and have has repeat old symptoms', JCV went ...

Hi all, I had my last Tysabri infusion yesterday and will start Kesimpta in 6 weeks. For those who have made this change, what was it like for you? I’ve been pretty symptom free for over year, so can I expect a flare up before the kesimpta has time to bed down in my system? Thanks

Has anyone noticed any heart problems whilst on Tysabri? I started having episodes of heart palpitations/irregular heart beats after my 4th infusion but my doctor dismissed it, that it’s not a side effect of the infusion just a coincidence… has anyone had anything similar? Thank you!