Hey guys, I was just wondering what some of your experiences on Cladribine has been. My MS team are pushing it on me as my next DMD. The way it works freaks me out… not having to take anything to a period of time. I’m used to a daily dose of Fingolimod or a weekly dose of Avonex. I’m getting huge amounts of infections on Fingolimod and that’s why they are pushing Cladribine. Also I’m raging as I had new lesions that developed in the last five years where I didn’t have a brain scan. So goodness knows how long Fingolimod hasn’t been working. Haven’t had a spinal scan since 2018 so requested one of those. Sometimes I think the teams can be utterly useless at explaining things… so I’d really appreciate the actual experts (people living with MS) views on Cladribine. Thank you for your time