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Hello all, you may remember that me and my brother-in-law met with an MP in Parliament, speaking about how PPMS folk in the U.K. are denied access to Ocrevus, and about how people in different constituencies and local authorities access better or poorer services depending on where they live. Have ha...

Hi MS warriors, how are you coping with the heat???

Hey everyone! 🌟 Just wanted to share a little bit about my journey with MS. Despite the challenges, I've come to see it as my very own superpower. It's a reminder that staying positive and resilient can truly make a difference. Let's keep pushing forward, supporting each other, and spreading hope. ...

Hello all. You may remember that I got invited to Westminster to meet an MP and discuss the refusal to approve Ocrevus for PPMS, which my sister has. My hospital has said that I would be eligible, as I’m RRMS. Well, the MS Society asked me and my sister if we would be happy to release our story for ...

How are you all coping with the heat in the UK at the moment?

Drop a special hello if you’re from or living in the DC area. 🙂 Sometimes I feel like the only one. 🤣 - I know that isn’t the case. 🙂

I need your help. Has n e 1 tried the CBD oil for MS symptoms like tremor?

Any one from Ireland on this I'm Tipperary