@Hajer1 

Last reply

Hajer1

Lost

So im not on any dmd im in Canada..i tried Rebif it sucks. I have acquired pendular nystagmus from a relapse it ruined everything all my plans and im trying to stay positive but its an earthquake for me 24/7. My neurologist is a b$$:c i wont get into that but she wants me on Cladribin oral form not IV. My appointment is in a week to discuss it but I want to know if anyone tried cladribin and was it any good? Thanks
@Stumbler

Hi @hajer1 , I've no firsthand experience, but there are some earlier posts. You can find them here :- https://shift.ms/?s=cladribine

@EdgarLeroy

I've taken a full course of the injections. It is very easy to tolerate. Blood monitoring is minimal. The clinical data says that it is as safe as any other MS drug and more effective than most all others. Only a few doses are needed, so you don't constantly need the drug in your body. It resets the immune system (induction). And it gets into the brain to reduce inflammation there as well. It has a lot going for it.