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 start a campaign on social media. I am not on facebook but have just come across the site change.org where you can start a petition to raise public awareness and get signatures. If all the people with M.S. and their friends and families signed we could get a lot of signatures, WHAT DO YOU THINK ? anything that keeps me out of a wheelchair for another 7 years is a result by me.!
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