Hi, does anyone take cladribine for ms ?if so, could you tell me roughly how long the side effects lasted for you ? I’ve been on Avonex since September 18 but my most recent mri showed up new lesions, one of which was active so I have been offered stronger drugs and I’ve decided to go with cladribine. I’m anxious to get started on it ASAP but if the side effects last for a while then it’s going to affect my daughter during the school holidays and I really don’t want her worrying any more than she does just now.


Sorry September 17

Hi look at Cladribine Users UK on Facebook. This page follows ms patients taking cladribine and their experiences. Or look at MS Shift where you will find plenty of info. Sue.