Hello,
I’ve just received an MS diagnosis and my consultant has offered me DMT with the choices of copaxone or tysabri. I was wondering if anyone has had either/ both of these treatments and could give me any advice?
Thanks!
Elicia
Hello,
I’ve just received an MS diagnosis and my consultant has offered me DMT with the choices of copaxone or tysabri. I was wondering if anyone has had either/ both of these treatments and could give me any advice?
Thanks!
Elicia
Hi, I will have been on Tysabri 5 years this September. All I can say is its brilliant, no real side effects apart from tiredness the day after infusion. I have been relapse free since being on Tysabri. Hope this helps.
Hi Elicia, welcome to the club
I was on Tysabri for 6 or 7 years. I had a similar experience as Irons. Main side effect was being knackered for the rest of the day after an infusion, but that’s about it. Hardly any relapses too. However, I eventually decided to come off it, as my risk of PML was getting pretty high (your consultant presumably said something to you about this?)
But as I always say to people, no decision is final. If you don’t get on with a particular treatment, you can always ask to switch.
Good luck
Dan