After Mr Musk ruined Twitter, I’m here to find my old MS pals and gain some new ones. I was diagnosed six years ago, I’ve been on Ocrevus and now Kesimpta (which I don’t find helpful at all). I’m working on my PhD looking at foot and lower limb health in people with MS (I’m a Podiatrist). I’m here for any questions, advice, or just a wave 👍🏻