Newly diagnosed
I was diagnosed with RRMS a couple of days ago, and I have decided to try Kesimpta as it seemed less invasive. Has everyone had a good experience with this, or what are the things I need to look out for? I have never had to be on long term medication before, so it’s all new to me. Any information/stories would be greatly appreciated
I have had ms over 16 years. I was on Copaxone for 15 years. Then changed to kesimpta 1 year ago. The loading dose gave me flu like symptoms but not issues after that. God Bless fellow ms warrior 🧡🙏
Kesimpta is a good choice. I was on Tecfidera 1st got a new liaison then was out on Kesimpta back in 23. Find this most comfy and miles better fo me. Helping in a massive way. Don't get me wrong we still have good days and days but still get buy if you but it behind your head and crack on trying to be normal. Good luck