Hi everyone,
I received my diagnosis today of relapsing-remitting MS. Apart from crying in the nurse’s arms outside the consultant’s room, I think I dealt with it quite well…
Doctor would like to put me on Mavenclad, and I should hopefully be starting that in a few weeks tops; does anyone have any experience with this drug?
I think although I was 98% certain I had MS before I was told today, it will take some time to fully process.
Hope you’re all doing okay.
L x
Hello L,
If you are on FB there is a closed group for UK Cladribine users (Mavenclad). The people in there are either considering, offered, taking or have taken this treatment. They are a kind friendly group with quite a lot of experience.
I took Cladribine (the injection form of Mavenclad) in 2018/2019 and everything went well with it.
I hope this helps.
MS2017
Thank you @MS2017, that is really helpful, I will take a look at the FB group 
I expect you have already been told most of this stuff already, but it’s from the professor of neurology at Barts and might be of interest.
Thank you @whammel, that is a super helpful link - will give it a read through