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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 💕

I am newly diagnosed and start my first bout of Kesimpta next week and would like to know what side effects I have to look forward to if any Thank you

So I went to the doctor my lession on my brain hasn't progressed so that's good but, I was concerned because I asked my doctor why haven't I been sick yet, my main worry was how often I would get sick due to it supposedly suppressing my immune system but, I have not maybe due to my other autoimmune ...

Hi 👋 i was diagnosed with RRMS january 2025 but have had symptoms from march 2021. Last thursday i started my first dose of Kesimpta - the injection itself was fine but the after symptoms were extremely intense for me that still 4 days later i feel off. Is it normal for you to still have sort of co...

Kesimpta users, update everyone here with how the medication has been for you. ⬇️⬇️⬇️⬇️⬇️

My doctor is changing my medicine, from aubagio to kesimpta is there something I need to know?

I started kesimpta tuseday and I think I'm having a relasp. Can starting a DMT trigger a relaps? I'm full of a cold too.

Hi there- I’ve been on Kesimpta since the end of September- I still feel rough some days, optic neuritis, headaches, dizziness, balance issues body aches and endless fatigue- everyone keeps telling me it will take time for me and my body/MS to adjust to treatment but when have these things started t...