Ocrevuz
Hi all. Im just wondering does anybody have info on the ocremuz infusion. I was recently diagnosed with ppms and am waiting to hear on an appointment date for the infusion, but in typical google fashion some are saying its brilliant and some are saying its awful. To make a long story short has anyone any experience with the ocremuz , im down to get it but know very little about it or its effects. Thanks
I think just like MS it’s going to be unique to you. I’ve been on it for a few years. I like the convenience of it and haven’t experience any major side effects other that tired and drained the week following the infusion.
to give you an idea how I feel about it I am curious sitting getting my 11th intrusion. You may not be able to tell if it helps but looking at an MRI you’re nuerologist will know. Only way I know is I also feel tired for a few days after infusion or as I say “I am infusiotired”