Looking for people who are taking Mavenclad. This is the medication my neurologist wants to try for me. I used to be on Ocrevus but I ended up getting breast cancer so I can’t take that medication anymore. I’m just looking for people who are on Mavenclad and how it’s working for you. I’ve been diagnosed with SPMS since 2015.. I was originally diagnosed with RRMS in 2009
Yes, I've been on it for 3 years. I have been on numerous MS medications, but none of them worked. I would go to my 6 month folkow up and have a new lesion. So, my neurologist said I had aggressive MS and put me on Mavenclad. I have not had 1 new lesion since I've been on it.
https://www.facebook.com/share/g/17uB1kLUX9/?mi...
How is Mavenclad working for people with SPMS?
Mavenclad (cladribine) is an FDA-approved medication for treating secondary progressive MS, along with RRMS and CIS. It works by interfering with DNA processes in certain immune cells to prevent them from replicating, which helps control the inflammation that damages nerve Show Full Answer
Sorry, no I haven't tried Mavenclad. I have SPMS. Hope you do well on it!
Yah I finished it over 5 years ago. Go on the mavenclad Facebook group