@dominics I was diagnosed with RRMS at the end of July. No one told me about the register but I came across it somewhere in my (endless) MS googling and immediately signed up as I liked the idea that I would be doing something useful. I’ve filled in as much data as I can though I’m not yet linked to my hospital – I am going to raise it with them during my next (phone) appointment. I was a bit taken aback at the amount of personal info I was prompted to give but I’m a trusting soul so felt comfortable with it overall. Happy if it helps really.