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Hi , I had my first Tysabri infusion on Wednesday . I felt fine after it & just felt a bit tired. I’m feeling a little off balance when I’m walking since yesterday. Just wondering if anyone experienced anything similar after infusion . Thanks

Just back from infusion #5 of tysabri and doesn’t seem to be making any difference at all...... Still original symptoms and new symptoms Anyone In same boat...? Also whilst I’m on, anyone got recommendations on CPD vapes?

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 ...

MS is stressing. We MSers know that first hand. Unfortunately seems that my boyfriend of 6 years is only now realizing that. We have been fighting a lot and he has said very hurtful things to me. Its true that he apologizes when his temper has cooled off but truth is that for the past few months we ...

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...

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 ...

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.

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...

Can anyone tell me if Tysabri infusions are free I have been recently been diagnosed with RR MS and will be starting this infusion soon. Are they free if you only have private health insurance 😊

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