I recently have been diagnosed and will more than likely start Kesimpta soon.
For what it's worth, I've read it's really effective. If mine stops being effective, I'm going to ask about this one next.
I've just taken my 2nd monthly dose today (20/12/2023). It's not been a pain for me injecting myself because I started off on copaxone, but I've noticed a difference in my abilities. I especially loved the difference during my 3 starter doses! I hope you find it works well for you 🫂❤️
Iv been on Kesimpta for 20 months now . At frist I would het headaches before and after the injection for about a week . Then it's slowly tapered off. After thar they switched companies where it came from . So the brain pain came . Not like headaches . Just pain in one location..Now though it's went away. My mris are clear. No new lesions and that's been right after starting Kesimpta.. I have 25 pluse on my brain and 9 in my spine. Bu t no new ones .
Hi! I’ve been on Kesimpta for 15 months. I recently had a mri of the brain and spine and have no new lesions or disease activity. I was diagnosed May 2022 so this is also my first dmt and so far so good. Best of luck!
I have been on it for almost 3 years and I don't particularly care for it.