Hello! I was recently diagnosed with RRMS, still trying to get through it and accept it. My doctor is putting me on Kesimpta has anyone been on this, what should I expect? TIA!
Hey everyone. I started kesimpta yesterday for the first time after being diagnosed in September 2025. After 4 hours I kept fainted, was dizzy and sick and ended up getting taken into hospital in an ambulance. Has anyone else experienced this ?
Did my first dose of kesimpta today. My head hurts, my body hurts. It's not the worse thing I've ever been through but it sucks. Hopefully I feel better tomorrow before work
Well, they wanted me on Vumerity but insurance put a stop to that so I am now taking the Kesimpta injections. Anyone else on these? How long before any noticeable changes if any? Any one else have some minor-ish side effects?
I was recently diagnosed with MS, and I’ll be starting kesimpta, but I’ve heard the loading dose is pretty rough, and I’m really never about it.
What has your experience been on it?
So my new specialist wants to start me on kesimpta in a couple weeks. It will be the first time I will be taking anything. She said that she believes I have rrms and that it's early. I really don't want to take anything right now seeing as I don't really have any symptoms. I don't want them to start...
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...