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something specific?

Prof G gives a great breakdown here. https://msselfie.co.uk/treatment-strategy/what-are-the-attributes-of-the-specific-dmts/

Hello! I am due for my next ocrevus infusion in October. My neurologist recommended I get yearly Covid and flu vaccines. Do you recommend this? I did it last year but I just hate the thought of getting vaccines all the time..

Apparently for pregnant women and older adults only. I'm not an expert, though I wonder why immunosuppressed people are not included like they are for Covid and Flu. Does anyone know? https://www.nhs.uk/vaccinations/rsv-vaccine/

I have Covid. And due my Kesimpta tonight. Does anyone know if I should delay it? I feel terrible with lots of Covid symptoms. Can’t get hold of my MS team. Thanks

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?

You have no controll of the future nor the past, dwelling on it isn’t going to change anything but make the present insufferable, stay focused on the now and what u can do not what u can’t do or what u wont be able to do later, I think with ms having so many possibilities it makes it impossible for ...

Hello all, I’m on my second bout of Covid but the first one whilst diagnosed with RRMS. I got Paxlovid prescribed on Day 1 and have been in bed for 3 days as I find the best thing for me to do is as little as possible when I don’t feel well. The Covid nurse (North Lancashire/South Cumbria) told me ...

One benefit of covid, other than people having to stay away from me (joke, I am actually really sociable!) was that I massively got into fitness, although you wouldn’t tell now! This was pre diagnosis, but I lost 2 stone (again, put most of it back on!) and I actually really enjoyed working out. I’m...

Hi all, I’m on day 3 of my first time having covid. It’s been rough but I’m hoping I’m starting to improve now. I noticed a small new numb patch on the back of leg yesterday which isn’t gone this morning. Has anyone had relapse or flare up brought on by covid? Really nervous that my kesimpta isn...

I have had my first lot of treatment in April due again October, so people normally get a MRI to check if infusion is working