Curious!
I am curious if anyone has switched from Tysabri to Ocrevus? I have been feeling like crap on Tysabri for about 6 months. I asked my neurologist about switching. She said that don't think it will benefit me so, said no. I recently told them to switch me due to not able to continue feeding like I do.
She finally agreed to allow it but, have to wait until this coronavirus is taken care of. I am wondering about how the switch was and if you felt better after the switch.
@cdrake , this question has been raised before, although the answers weren't quite specific :- https://shift.ms/topic/switching-from-tysabri-to-ocrevus
@drakec (sorry about getting your name arse-about-face above), I found some blog posts about this treatment switch, which you may find useful :- https://multiplesclerosisnewstoday.com/2017/07/06/ms-ocrevus-and-me-switching-to-new-disease-modifying-therapy/ https://multiplesclerosisnewstoday.com/2017/07/13/ms-ocrevus-and-me-part-2-infusion-time-side-effects/