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My ms journey has transitioned to SPMS. I am in my second month of starting Kesimpta. for those of that use Kesimpta what improvements did see? Not a cure, did you have any incremental improvements? Also, has anyone used Botox shots to help manage a foot drop. I’m trying to learn how to manage the...

Anyone feel like some MS symptoms return a few days before getting next shot? Started Kesimpta in June and a lot of my symptoms ( spasticity, tightness, tingling, back pain, ms hug) vanished after third weekly shot. Now I’m on the monthly one and am due my second monthly shot but the tingling has ...

I am starting to get really nervous, almost to the point of wanting to postpone... I was just diagnosed last month with RRMS and I am supposed to start my shot on either sunday or monday. Any advice or tips? I am so scared of the possible side effects with the loading doses...

Hi guys, My Dr. is trying to change my medication from Tecfidera to Kesimpta since its better and stronger for me . Does anyone have any advice or suggestions? Should I do it? Did anyone get any infection problems because of this medication?

I’m due to have my first dosage of kesimpta on Friday, the following Friday I’m away… question is do I do it on the eve or keep it same as the morning like I’m having this week? Also would I be able to keep it in a cool bag? Thanks in advance

Doctor has been talking to me about starting a long acting injection. I'm nervous about it. Anyone on here take the medication and has it worked for you?

Those who are on Kesimpta, have you forgotten to inject on the day you're due? I know it's only a month at a time but how do you keep up remembering and prompting yourself?

I took Kesimpta for 5 mos. and was never so sick in all my life. Pneumonia twice, Covid, bronchitis, an abscessed tooth, colitis, a rash ECT....Anyone else have a reaction like that and what meds are good? I've been on Copaxon, Kesimpta, Avonex, Tecfedera, and Achtar steroid but had bad reactions to...

So had my first MS nurse appointment today and I’ve agreed to start kesimpta. I did want ocrevus but would have to travel far which not really wanting to do. So what’s peoples experiences of kesimpta please?

I have been off DMTs for a long time. I'm going to be seeing a neurologist here mid June. I was going to see about getting on Kesimpta. Is anyone currently taking or has taken this? I'm just wondering how it's worked/working for you and what your experiences have been like. Much love 💕