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I'm wondering if any men have experienced fertility issues? I'm on Ocrevus and wondering if the drug (or MS in general) can affect my sperm count/motility. Was it harder to conceive or were you even able to get your girlfriends/wives pregnant at all?

A couple of people in another MS group I'm in have been told they can have their next infusion but they will have to self isolate for 12 weeks after. Anyone else had this ?

Hey guys. I hope you are all well. My ms nurse phoned me today to tell me some good news....... I can start ocrevus in 4 weeks time. Whoop whoop. My question is I have a 3 year old daughter and a 2 year old dog (who eats everything he is not supposed to) what advice can you give for me to protect...

Does anyone know if they have started ocrevus infusions at kings London again yet? I was due to start infusions in March but it was obviously cancelled. Told I was near the top of the list but haven’t heard anything. I have been waiting since September. 2019

Started Ocrevus in October last year, my first full dose was due in April but obviously got cancelled due to the Corona virus. It’s been rescheduled for 23rd June (day before my birthday) . I’m just really hoping I’m not told to shield afterwards. Has anyone who has received their treatment lately ...

Hi all, hope everyone is doing well. I just have a question...I've had MS for a few years now, rapidly evolving severe, I've had 2 courses of lemtrada but after 1 year of my last course I had new activity so my neurologist put me on copaxone injections. I wasn't eligible for ocrevus as my immune sys...

Hi, I was reading through some ocrevus posts, and I started wondering - have any of you on Ocrevus caught covid yet? Or are you all still isolating?

I was diagnosed last year, i thought I was lucky with relatively light physical symptoms. Balance, some pain but cognitive problems are really starting again.............. Does anyone have issues of trying to make simple calculations work in your head? I find it difficult at the moment. I'm trying t...

Hi all, I am supposed to be moving to Ocrevus soon. I have 1.44 JSV antibodies and the docs here are scared that I will get PML. My 2 years on Natalizumab (Tysabri) is up on 2 Oct 2020 and they want me off Natalizumab really soon. My problem is that I am allergic to many medicines and had 5 weeks...

Can someone help me? I’ve searched the web and all the MS sites and can’t find the answer. I would like to hear from someone who has symptoms daily that come and go. Like everyday. For instance I permanently have numb feet but sometimes in the day it travels up to my knees then goes away back to jus...