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.
thanks