Beth, I am 69, diagnosed with PPMS in 2014. The following will explain why at this point in time I chose to not try Ocrevus.

I have followed this topic since I was first diagnosed. We're all different, but for me and my condition it is still a no.

http://www.wheelchairkamikaze.com/2016/03/ocrel...

Thanks for the link Ed...very good read. Since my first dx was SPMS I have never received any rx for it. Thus have been left to my and God’s help and I can truly say, I am satisfied with that. Everything I’ve taken has been natural like biotin which is vitamin B7 And megadoses of vitamin D3 with K2 and megadoses of B complex, magnesium, ALA twice a day at 600 mg… And I repeat no side effects, only benefits. My journey!

Thanks for sending the Link Ed !!
I’ve made my mind up

Thanks for the link... gives one pause. Thank you for sharing

What makes you feel so strongly against ocrevus? I haven’t read any major indication that would drive me away from it. Are you seeking any treatment.. I am newly diagnosed with PPMS and have gone through on infusion. Maybe time will tell but I am willing to give it a try.