Tysabri
I am on Tasabri infusion.. Have had three so far going be every four weeks .. Been told it will reduce relapses which I have had four in last 18 months.. Anyone any feed back what I can expect ... Thank you
I've been on it for a few years,I have ppms,since I've been on it my mri's have showed no active or new lesions, it has been the best thing for me,and I have been on copaxone,rebif and betaseron. I'm so thankful for this,I've been able to do things I couldn't do for years like simple things,crossing my legs,laying on my stomach!! I love it!!
I'm on Tysabri also - I have secondary progressive MS - it has stopped new lesions from forming on my MRIs - slowed down the progression π I have been on it 2 years
Me too DBrian
I was on it and it worked well but I started producing antibodies and had to stop.
I have been on it since 2012. No major relapses as such, just a few niggly symptoms. I find I feel great for 3-3.5 weeks then feel a bit knackered in the few days running up to next infusion. Other people report feeling a bit tired the few days after having it. Just take it easy and hopefully it will suit you.
Elevated Heart Rate With Tysabri Has Anyone Experienced This. This Is My Second Time And I Am Going To Stop Tysabri
Anyone Have Had Treatment With Tysabri? What Has Been Your Experience?
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