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Hello everyone. Does anyone in this community take Ocrevus?

Hello Every one I want to know how it is wen startiing ocrevus does the fatigue go sky high and spasms in crease and energy loss, pains in arms legs and feet issue walking? Woukd really like to know before I start calling my ms team as they do take time to get back. Thanks

I was just diagnosed with RRMS a couple months ago. I am getting my first infusion on Wednesday next week. Any tips on what to expect? Or any advice? Thank you.

Hey everyone, have registered with this site a couple of years ago but only downloaded the app last night never knew it was a thing till I saw it on an advert while watching a Facebook video! What a great app and support for all. So, I received a letter the other day from the MS coordinator for So...

Anyone tried the quicker treatment. ? It was mentioned to me it might be available for me next time which is March

Went for my infusion last month and there’s already talk around the hospital about ocrevus being given as an injection instead of an infusion. Not sure what I think yet 🤷🏼‍♀️has anyone spoken to their neurologist about this yet?

Here i go for my 2nd infusion. Wish me luck.

I am waiting to star this as my new treatment having had a few others that have not worked well for me I’m a bit nervous about starting, how have others found this drug ?

So, I've had my 2 half doses of ocrevus and feel like I've been poorly non stop since having it. Does this calm down? Just questioning if I have made the right treatment decision 😕

So I’ve been on Tecfidera for about a year and a half and apparently my body wasn’t responding to it as it should. My doctor suggested I start Ocrevus, with my first dosage being on the 12th of September … I’m honestly terrified and idk why tbh. Any advice? 🥺