Have you tried Ocrelizumab (Ocrevus)?

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Patients Multiple sclerosis

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Posted on

Hello all,
I've been doing some reading about possible treatments and I read that ocrelizumab can now be given to people with RRMS and I've heard it really does wonders. Has anyone on here been on it? Has it worked for you? Did you have any side effects? I'm curently taking Avonex and it's really not working. I'm due for an appointment soon and I'm afraid I'll have more lesions, so I'm thinking of asking my doctor about Ocrevus. Any advice is appreciated!

Beginning of the discussion - 15/07/2020

Have you tried Ocrelizumab (Ocrevus)?

Posted on

@nameless Hello nameless, thank you for opening this discussion. Let me tag some members who may have some feedback for you on Ocrevus.

Hello members, how are you today? Have you been on Ocrevus for your MS? What do you think of it? Has it helped you with your MS? Did you have any side effects? Feel free to share here!
@Sandy12@Claire1974@Cherylmoore@Davbod1870@Carol50@Granmarshall@Barbershop19@NicLiv@ANGIE.@Kimskin@Jowilliamson82@Querky@MSWarrior123@Bonnyvonny64@Amy1977@JuWall76@Vwelwood‍ 

Take care,
Courtney

Have you tried Ocrelizumab (Ocrevus)?
1


Posted on
Hi. I was put on tysabri from the onslaught.... after 2 lots of steroids and a plasma exchange, as my rrms was so aggressive and unforgiving.... but ive now been on it literally a year and, touch wood, it's working & my 1st check up mri showed no further lesions or features of PML....so if you find something that works stick with it aslong as you can xx
Have you tried Ocrelizumab (Ocrevus)?

Posted on

I’m a little confused because I have a telephone appt on Weds I’ve had ms now for nearly 30yrs and had beta interferon, avonex and 2yrs trial on ya blood interferons. (Intravenous). My ms atm is starting to worsen I suppose I’m blessed to have had 30yrs being physically able but not anymore. I have spms so was wondering about asking about the Ocrevus, but there in lies another problem I have two slipped discs in my back and have to have an op on my back, I’m worried about it because it’s on the spine and would it interfere with my ms? So many questions sorry 😐 but any advice appreciated. Btw shout out to anyone who attends the Royal hallamshire Hospital I have a new consultant and his names Dr Lindert? Anybody know of him? And what he’s like? Thanks 😊 blessings to you all