Photo: Group of people with MS and their networks at the KGBTMS photoshoot 2018

Our work

Our vision is a world free from the effects of MS.

Our ultimate goal is to find a cure. Until then, we're working to make sure no one has to face MS alone. Everything we do is guided by people with MS. Because together, we're stronger.

Connect with people online

Join our community

Our story

Here for everyone with MS

We're the MS Society, we're a community of people living with MS, researchers, fundraisers, campaigners and volunteers.

We know together we're strong enough to stop MS. And we're working hard to make it happen.

Watch our video to find out more. This version has audio description.

In this section

Photo shows three people in MS Society T shirts grinning and waving noise sticks

How we work

We’ve got ambitious plans for MS treatments, research, care and support. And we work with our community to make them happen. Together, we can stop MS.

Find out more about how we work
Photo: poster advertising MS Society inaugural meeting in Chelsea in 1953

Our history

Since our first meeting in 1953 we've grown from one friendly group to hundreds across the UK. We've funded world class research and seen incredible breakthroughs in treatments.

Find out more about our history
Photo: Research working in the lab

Research

Our vision is a world free from the effects of MS. And we're getting closer. In today’s money, we've invested over £218 million in research since 1956.

Read more about MS research

Campaigns
Too many people affected by MS in the UK have to fight for the treatments, services, care and support they need. Our campaigns help change that.
Find out about our campaigns

Policies 
Everything we do is underpinned by research and informed by experts in MS, policy and research.
Explore our policies

Evidence
Our evidence underpins everything we do. It's one of the ways we can make sure we're using our resources to make the most impact we can.
Read our evidence
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Find support near me

From support groups to information events, there's lots of ways to connect with people who understand what life's like with MS.

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