Do people have ocrevus subcutaneously or IV?

looks as though the first trials /phase will be on healthy people. If ok no side effects detected then the clinical stage. GPR17 for Remyelination .They say maybe upto seven years until we get it .Not sure if anybody can find any more info on this

Anyone on Tysabri? and what are you’re thoughts about it…I’ve been on it a year now

I was told by a neurologist a few years ago that as a patient with MS gets older they tend not to need immunosuppressants. Has anyone else heard this?

Do you experience challenges with your speech? If so, could you share your experience and any tips that have helped you? Lately I've noticed my speech can sometimes be affected, and I'd love to hear how others manage it.

I just spoke with HR about increasing my FMLA due to new worsening of some symptoms. Mind you this is a RN in HR ... She asked if it's this a lifelong illness? Then same conversation "I have a friend with MS that does the infusions too and he's doing very well". .... If she could have seen the look ...

So I a question.. MS seems to UTIs.. does anyone recommend anything to use to help this? I was recommended cranberry juice, raw cranberries, cranberry pills.

Ladies, I need advise.. As I am a organised woman just wanted to know in advance if you can breastfeed with Ocrevus I am due to give birth early December but my infusion will not start again until 2 weeks after giving birth. Any help will be much appreciated on this, I Thankyou! X