Hi I was diagnosed in January this year with RR MS I have been on interferon rebif injections (due to ms attacking my eyes) came off that then tried Tecfidera, that made me very sick so had to come off that. At the moment I am on nothing but again the MS is attacking my eyes so doctors need to get my MS under control before can sort out my eyes. I did some research on ocrevus infusion and wondered if anyone had some advice or other medications. My nurses said my only other form of medication word be injectables. Would welcome all help and advice 
I am just waiting to start Tysabri for very active RRMS. All the reviews I have read have been very good. I have also spoke online to people who have it and have heard 99% positive experiences. The MS Nurse said it’s the one she would opt for if she were in my position as it’s proven to be very effective. It’s an injection every 4 weeks at the hospital, it used to be an infusion but has changed now. Worth looking into. My other options were Ocrevus, Kesimpta and another one I don’t remember the name of. I didn’t want Kesimpta as I don’t want to inject myself and I felt Ocrevus had more side effects than Tysabri. I think the other one I was offered is mainly aimed at women who want children in the near future.
Hope this helps
Jx