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First half dose of ocrevus started today roll on two weeks to get the other half hope everyone having a good day

last month i had the injections for tysabri, this month i got the infusion and had the WORST reaction (hives, sweating, pale, nausea, fatigue, black out, sore throat, chest pain, rapid heartbeat etc) anyone know why i reacted this way to the infusion but not the injections? thanks baes xxxx

The first half dose of Ocrevus went very very well, I am pleased to say all looks good so far:D I am very grateful to have the opportunity to have this treatment! And thank you to all the NHS infusion staff at St Georges Hospital, an absolute pleasure to have them take care of everyone there!!:)

Receiving my first infusion 17th march a bit nervous

October 1st can’t get here quick enough...... been off my infusion since July because I moved out of state 🤦🏾‍♀️🧡

Has anyone else had a rash across face from steroid infusions ? I had clear skin before now a rash on ny face that doesnt go away and no medical people are really helping

Had my latest infusion yesterday for Ocrevus, 4th full one... all went well but tired and battered now....

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...

Curious if anyone gets infusions after normal business hours or on the weekend. I got a new job that is very busy and don’t want them thinking I’m an employee with a disability that takes off all the time. I know I’m protected by ADA but rather them not know until they need to. Thanks!

Curious if anyone gets infusions after normal business hours or on the weekend. I got a new job that is very busy and don’t want them thinking I’m an employee with a disability that takes off all the time. I know I’m protected by ADA but rather them not know until they need to. Thanks!

Tomorrow I get my 2nd infusion, hopefully I won’t get a rash or hives this time.

Didn't get a rash or hives this time, but only got really sleepy. Got it done much faster than last time and I watched the Mask of Zorro, great action. Next one comes in Sept.

I finally got my 1st infusion with Rituxan. I did get a bit of a rash on my body and hives on my back at first, but the docs were able to reverse everything and still give me my treatment. I got to watch Wednesday with my parents on Netflix (on a Wednesday hehehe). Definitely going to enjoy my res...

Tomorrow I finally get my first infusion for Rituxan, pretty nervous. I’m curious if anyone on here has received Rituxan as well?

I finally have a date for my 1st infusion, Feb 22 and will be injected with Rituxan. A bit of good news after a shit day at work today.

I was diagnosed with PPMS in August 2022 after a series of MRI's My MS Neurologist prescribed Ocrevus, my first infusion was December 2022 split in to 2 appointments 2 weeks apart... 2-3 hours sitting with a needle in my arm went better than I thought, symptoms were tiredness and dizzyness while wal...

Nhs asked would i move from infusions to injections, I Dont want to and don't have to, but i will change to injections as it helps others get access to treatment. Anybody made the switch. Good idea or bad idea, i guess i will see. 🤔

Thoughts anyone?? https://pubmed.ncbi.nlm.nih.gov/36639226/

Hello everyone!! I had my natalizumab infusion today and I’ve only just noticed something that happens every time. My face (especially cheeks) go very red and I look very puffy and swollen over my body. It looks a bit like a minor allergic reaction - is this normal? And does anybody else get a react...