Ocrevus
I haven't been on here for a very long time and just wanted to share my experience of Ocrevus for those of you who are about to start it. Ocrevus is the first treatment I have had since being diagnosed with RRms in 2018. I have been having it now for nearly 4 years I think. For me it has been absolutely fine every time. I have felt a bit tired half way through the day but I think thats mainly because I have to get up at 5am each time to get to the hospital. I normally have a headache by the end of the day as well but have felt absolutely fine the following day. Touch wood I have had no other MS symptoms since starting it either. I just hope that continues......
Thanks for sharing, I hope it will work work well for me so far good but I only had the first two half infusions due for the first full one next Monday.
You will do fine but the drug company just approved a super fast infusion, whatever it is like 2 hours i would say stick to the 3. I have been on it for a while and that short infusion knocked me whacky for a couple days. Malibubond