How fast do people see changes after there infusion? And what kind?
I have been on tysabri for 16 months. I originally expected dramatic and immediate results. That didn't happen but that isn't to say that the changes have not been dramatic. When I started, I could barely walk, dizzy all the time and bone-tired. I was scared. Really scared but look at me now. I can walk long distances, my balance. Is great, lots of energy. You just couldn't see where I was headed until I got there. My husband and I think back to what I was doing a year ago and am amazed. So, stick with it and I hope your journey is as good as mine.
@A MyMSTeam Member Great to hear Tysabri is working for you. Is there any side effects for you? I don't think it is available in Canada or I haven't heard of anyone on it. Sounds great for you.
I really didn't notice a difference when I switches from COPAXONE to Tysbari however when I went without my infusion for 10 weeks I notices the effects of the MS, fatigue, weakness, balance issues, tingling sensations. After receiving the infusion I'm usually tired I'll go home and sleep, on the following day I did feel a lot better.
Thanks so much @A MyMSTeam Member ....I'm praying I also have even a bit of that success....so it seems it just starts improving things very gradually.... To quote the grateful dead.... "I need a miracle"
I had to go off tysabri because I was JC positive. It eliminated my hand tremors and my balance seemed improved. I noticed it about a few months of treatment.
Newly Diagnosed. My Neurologist Recommends Tysabri (infusion). Is Anyone Else On This Treatment And How Is It Working For You?
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