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Hi all 👋. Just a question about Ocrevus treatment. Just wondering if anyone knows of any reason why I wouldn’t receive my infusion? I am concerned that I will catch my child’s raging cold/cough. My infusion is due soon and I am concerned it may be delayed if I have the lurgy. 🤷‍♀️

Hello 👋 I’m in Scotland and newly diagnosed with RRMS a couple weeks ago. I’m trying to decide which treatment to go on. It needs to be a highly effective one. My neurologist and MS nurse are very much in favour of Ocrevus. We have also discussed Tysabri but they are pushing me more towards Ocrevu...

I have my first Ocrevus infusion tomorrow. Excited to be starting treatment but also very nervous. Just hoping this treatment works for me 🤞🏼

Hi everyone, I've just had a relapse while on Gilenya so I'm going to be changing treatment to either Tysabri or an antiCD20 molecule like Kesimpta. I was wondering whether it gets progressively more difficult to find a vein for iv access once a month while taking Tysabri? Also, does anyone have ex...

Hello, I’m new here, I’m 38 and I’m in the uk. I’ve been diagnosed for about 5 years with relapsing remitting. I generally get EVERY side effect (for example Tecfidera caused me to lose 2 stone) After my MRI at Christmas my neurologist described me as ‘moderately severe’ and after that things have...

I’m stressing. I’ve had RRMS for 10 years. Both MS nurses resigned recently at my hospital. My Ocrevus treatment was never scheduled, luckily I rang to find out what was happening, so I’m a month late having the infusion. Now a relapse… Does anyone know if I should even consider steroids it being ...

In case it's of interest to anyone, here's my diary of a first Ocrevus infusion. The day before, I was advised to drink a lot of water. Being hydrated helps the nurses find a vein. Got there at 8:20 for an 8:30 appointment, and was ushered straight through to a comfy chair. My blood pressure, hear...

Hello! I was wondering if anyone had any advice regarding the washout period for Ocrevus? Before trying for a baby. Has anyone had any experience of getting pregnant after Ocrevus? And how long did you wait before ending treatment and trying? The advice I was given originally was 12 months and have ...

After had first Ocrevus infusion Wednesday (half second half in 2 weeks) ever since body has seriously no energy. Muscle pains, no appetite, seriously lethargic just want to sleep constantly. I have no idea what the 🤬 is happening. Body feels like it's shutting down or something 🤷‍♂️ Anyone else h...

Hello All, so I wanted to ask for advice and guidance regarding treatments that have been offered to me. I have RRMS newly diagnosed in feb 2023 .. I’m still recovering from the horrible relapse I had and have a few days left of my steroids to finish. Saw a MS specialist last week who overwhelmed me...

Hey y’all I started ocrevus today, had my first half dose. I had itchy ears, mouth and throat but it went away pretty quickly. Right after I felt like I had a mild flu. Light aches, headache and fatigue. Not bad just enough to be uncomfortable. How did you guys feel after taking it?

Switching DMT and have been given these two options? I’m on tysabri now and it’s been a miracle for me but due to high JCV titre I can no longer be on it and I’m so very anxious about the future and relapses as I’ve been stable and the same for 2 years. Which is best from peoples experiences? Side e...

Hi everyone, I spoke to my neurologist today and I am swapping to Kesimpta in July from Ocrevus after 2.5 years. I am swapping because Ocrevus leaves me feeling so wiped out pre and post infusion. I’ve also been getting chest pain and I think it has stemmed from Ocrevus. I also got infusion reaction...

I’m wanting some advice. I started with symptoms over 2 years ago and un be known to me it was MS. I was given a lumbar puncture and had follow up scans throughout the year. In that year my walking became worse, balance and fatigue too. I got a diagnosis of PPMS in Dec 2021 but was told I didn’t mee...

hi everyone! I have recently been diagnosed with RR MS. I have new lesions in my brain, and they have offered either Kemsimpta or Ocrevus. I am leaning towards Ocrevus because the thought of injecting myself scares me but i wanted thoughts or advice on anyone who is on both and what are your side ef...

Today is day 1 of Ocrevus. I'm 31.7ml of this infusion in. Only another 3h 27m left 😂 🤞🤞🤞

Hi all, New at this place I directly wanted to push a question into this great community. I have PPMS and I am under Ocrevus now since mid of 2017. it’s my first medicine since the diagnosis 2017 and at this time I didn’t really feel ill. Now 5 1/2 years later my walk is heavily effected and I fe...

I had my first Ocrevus infusion on Friday morning and since then nausea has gradually become more intense. I’m now sat on my bathroom floor feeling like death, stomach is in so much pain and I feel like I need to be sick but can’t 😩 Has anyone got any advice?

Hi everyone. I’m hoping you’ll be able to help. Where I live there isn’t a big MS community. I find myself a bit confused and no one to ask really😞 I got diagnosed in October 2018 with RRMS. I’m on tecfidera since. In December last year I had my MRI and my neurologist told me I’ve got 2 new lesio...

After taking oc 4 years now i cant walk,i have lot of ms friends that are in same problem like me after oc. Now im one year oc free and i feel much better