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 💕
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...
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...
I got my first Kesimpta injection 10 hours ago. After 3 hours I started to experience flu like symptoms. After 6 hours I started to get a fever so I took Paracetamol. Now (after 7 hours) my heart rate is increasing to 115 in a sit position and 90 when laying down. Is this something to be worries abo...