So this is a little bit daunting as I’ve never actually reached out since my diagnosis. Firstly, here’s a little bit about me. My name’s Holly & im 26. I was diagnosed with MS in July 2021 after mri scans and lumber puncture from suffering leg numbness, blurred vision and speech problems. My mum who sadly passed away this year also had MS for roughly around 10 years so I reckon I just sort of had a gut feeling that it was the same. I haven’t really reached out to anyone regarding my ms or how I’m coping and have just sort of got on with things with help of my boyfriend & close family but it’s a bit of a taboo subject with them as they’re finding it difficult to deal with. So yeah, that’s me. I hope i can be part of a community where we don’t actually feel like we’re alone😊