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Hey everyone! Where you from? I am from WV!!!

Just wondering if anyone else out there has made the switch to Tecfidera? I used to be on Copaxone but hated the needles so have switched to the pills! They're not going so well at the moment! I'm on week 3 and have terrible cramping in my stomach, nausea, headaches, bloating, indigestion and reflux...

I was diagnosed in 2021. I was told by my neurologist my MS was a death sentence and i had 7 years left to live. Has anyone else heard this before?

It struck me this weekend that people with MS are actually probably particularly well equipped to deal with the coronavirus outbreak. Compared to the rest of the population, we are all used to: - Being stuck in limbo, nobody can ever tell us how long something will last and if it will be permanent,...

UPDATE: It is a flare up Since New Year's eve I feel a weird numbness in my feet, legs, the whole hip area and most of my upper body. It's a new symptom and as I said started around a week ago... and I feel like it gets worse... the numbness in my feet is now more of a feeling of tingling... quite ...

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 wh...