About Us

We’re the MS Society – a community of people living with MS, scientists, campaigners, volunteers and fundraisers.

We understand what life’s like with MS, and we support each other through the highs, lows and everything in between.

And we’re driving research into more – and better – treatments. For everyone.

What we do

We fund world-leading research, share the latest information and campaign for everyone’s rights. Together we are a community and together we can stop MS.

We understand what life’s like with MS. And we know together we are stronger. We’re researching, writing, campaigning and fighting. Running, walking, caring and talking.

Together, we are strong enough to stop MS.

Multiple sclerosis (MS) is a neurological condition – that means it affects your nerves. You get it when your immune system isn’t working properly.

Your immune system normally protects you by fighting off infection, but in MS it attacks your nerves by mistake. Your nerves control lots of different parts of your body. That’s why you can get MS symptoms in many parts of your body. It’s also why everyone’s MS is different.

Once diagnosed, MS stays with you for life, but treatments and specialists can help you to manage the condition and its symptoms. We’re here to help you live well with your MS and fund research to stop MS for good .

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