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Access to MS treatments

People with MS need timely access to professionals across health and social care to best manage their condition.

We want to see all licenced treatments for MS made available on the NHS, across the UK.

How we decide our policy positions on access to treatment

Our positions are based on multiple sources of evidence, including 

  • our My MS My Needs survey 2016 which had 11,000 respondents with MS
  • policy roundtables with local commissioners, clinicians and healthcare providers, and people living with MS across the UK.

Our policy positions on MS treatment

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Treat me right

We're campaigning for the right treatment at the right time for people with MS, whatever your situation, wherever you live.

Join our Treat me right campaign
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Our work in government

We make sure that politicians across the UK understand the issues affecting people living with MS.

Read about our work with government
Someone filling in a questionnaire

Our evidence

Our evidence underpins all our campaigning and policy work. And it's crucial for designing services that work for people with MS.

Explore our evidence