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Hi , I was diagnosed last nov with MS . I have been on Copazone since jan but after a second relapse I was told it’s not working . I’m starting Tysabri on the 17th July . Just wondering if there’s many side effects . I’m still getting my head around the diagnosis. Sorry just another question , I’m ...

Hi all, I wondered if anyone could help answer some questions/give their experience.... I was diagnosed in May this year with rapid RRMS following loss of sensation/power in right leg/Side in December 19 and then optic neuritis in April 20. First MRI was in March 20. I was originally told I would r...

Hey guys, so I’ve finally got the call from Neuro Daycare and I start on Tysabri on the 17th What should I expect, what are others experiences with this ? :)

Hi all, I am supposed to be moving to Ocrevus soon. I have 1.44 JSV antibodies and the docs here are scared that I will get PML. My 2 years on Natalizumab (Tysabri) is up on 2 Oct 2020 and they want me off Natalizumab really soon. My problem is that I am allergic to many medicines and had 5 weeks...

Hi my name is Erika Iam 32 years old, I was diagnosed in 2012, am taking tysabri. I got married two years ago( I have a 14 year old son now, doctor said am stable and am good to start planning on having a baby but for that I would have to change my treatment to Ritaxon, I’ve read it’s good to start ...

Morning! I was due to start Ocrevus but this has been put on hold due to the current pandemic. I’m currently waiting to commence tysabri instead. Just wondering if anyone else is in the same situation? I had been on Copaxone but the injections were leaving craters all over me and between the burnin...

I am going to be taken off Tysabri due to high Jcv. I have been told I will be offered either ocrevus or gilenya. So confused, if anyone can let me know how either is working for them I would be very grateful.

I was diagnosed in June 2019 having woken up with pins and needles in my hands in January. No previous symptoms. Pins and needles extended to whole body from chest down and I experienced MS hug a few times. After a couple of months things seemed more or less back to normal and although the pins and ...

Hi all, just looking for some advice... Has anyone experiened pelvic and leg pain after their tysabri infusion?? I started my first infusion nearly 2 wks ago and since then the pain in my leg is driving me crazy

<p>Anyone else made this same transition and for people on Tysabri how do you find it </p> <div class="i-support-link"> </div>