We involve people with MS at every stage to make sure our policies reflect their views. All our policy positions are decided through rigorous research and evidence gathering.
You can find our most up to date published position papers, government consultation responses and reports here. Any questions please do contact us.
How we decide our policy positions
Our positions are based on multiple sources of evidence, including
- our My MS My Needs survey 2016 which had 11,000 respondents
- focus groups
- surveys of people with MS
- independent research.
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.
Together, we are strong enough to stop MS.