Ocrelizumab
Hi I have PPMS, diagnosed last year. I've just been sent a letter offering me this treatment. Does anyone have any advice or experience that they can share?
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I’m on Ocrevus, but I’m diagnosed with RRMS. I have been on it for nearly a year and a half. It’s been a good drug for me, so far. Definitely recommend looking at UK MS charity sites. These can help weigh up DMTs and give clear information about them. There are tools which can help with comparison of DMTs. All the best.
on it too . About to have my 1st MS birthday next month . my nuero refused to label my type of MS until after my first year so he can get me on treatment ASAP and monitor on my annual MRI . from my own research I am looking like PPMS too and from that research Ocrevus is the only current treatment for PPMS. think that why he didn't want to label me straight away but went for the big guns as he called it straight away . regardless from my research I think I still would have chosen it .... wouldn't fancy self injecting myself every 4 weeks