I am in the extended study at Ohio State. I have RRMS and so far it's working really well.... I had an MRI in December before the last infusion and there was no new damage, so for me OCREVUS is great. No real side effects.

Scroll to the bottom, or look on the right to see a very informative video about @Ocrevus from the Cleveland Clinic that everyone needs to see before you decide to take this drug, especially those of us diagnosed as PPMS.

http://my.clevelandclinic.org/departments/neuro...

First PML case reported, patient had previously been taking Tysabri

https://www.google.com/amp/s/seekingalpha.com/a...

@A MyMSTeam Member, I was told I have PPMS but I don't know exactly what the difference is. I suspect one leads to the other and so on. I've been on Copaxone then tysabri then aubagio now tecfidera. So I'm pretty sure no matter what Meds they put me on this thing will do what it wants to do. And I'm cool with that, After 48 cancer treatments and now MS treatments, I'm good with whatever comes in front of me. I still have 2 years left before they consider me cancer free anyway. I really don't worry about tomorrow. I figure tomorrow will bring it's own challenges anyway.

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A MyMSTea...

I have an appointment tomorrow with my neurologist. I've read a lot about it. I'm going to ask. I'll let you know