Hi 👋, First time 'poster' here - hoping to get some thoughts on people's experiences with Plegridy. I'm currently awaiting delivery of the drug so should be starting it in the next couple of weeks. I've read some alarming stories about the drug online and am wondering whether I've made the right choice. I've also read a few of the older posts about Plegridy in the forums but wondered whether anyone had more recent/longterm experience of using the treatment? I've only just recently been diagnosed after being hospitalised with a sensory transverse myelitis and double vision (although I've had a suspicion I've had MS for a number of years now). Any advice/thoughts on Plegridy would be greatly appreciated, and looking forward to getting involved in the Shift.MS community going forward! Thanks 🤗