Hi all having P.P.M.S. I was looking forward to ocrelizumab as the only treatment, that is until the nice people at N.I.C.E. said they wouldnt pay for it. I feel really let down , and angry having paid in to the system all my working life , I am wondering if others feel the same, and if we should…
57 conversations about Ocrevus
Hey! My neurologist thinks Ocrevus is the best choice for my early PPMS. Because of insurance paperwork, I have to wait until march-june 2019 to get it though. Is there any benefit in starting treatment with βIFNs (Rebif or Betaferon/Betaseron) for less than a year? Or would you wait to start Ocr…
I have my first half dose of ocrevus tomorrow. I’m super excited and nervous at the same time!
Hi everyone just a question I have been taking L.D.N. for about 10 months just been offered Ocrevus by my Neuro who does not agree with L.D.N. so a bit nervous to say I am taking it one gentleman I spoke to says his wife has been taking both for a while and she is fine any comments
This is hot off the press and has upset people in the medical profession, as well as UK PPMSers. There’s already a campaign to contest this decision :- https://signup.mssociety.org.uk/page/30088/petition/1
Hello everyone. I just joined but I have been diagnosed since 2013. My last MRI showed new lesions. My neuro wants me to try Ocrevus. Is anyone on it? How do u like it? Any info would be greatly appreciated.