Treat me right
People with MS should have fair and equal access treatments wherever they live. But this isn’t happening. Our award winning campaign plans to change that.
We’re campaigning to make these goals a reality:
- All licensed MS treatments available on the NHS to everyone eligible for them
- Regular reviews of treatment and care by MS specialists for everyone with MS
- Accessible information about treatment options, and support to be equal partners in decision-making, available to all people with MS
Treatment for progressive MS
After 21,000 of us spoke up for ocrelizumab, NICE have approved it to be available on the NHS in England for people with early primary progressive MS.
Is access to treatment still a lottery?
Our research reveals that potentially thousands of people with relapsing forms of MS haven’t seen an MS nurse or neurologist in the last year or more.
Among this group, just 12% are taking a disease modifying therapy (DMT) which could help reduce relapses and slow progression.Read more about our research into access to treatments
Cannabis and MS
Since the start of Treat Me Right, we've been calling for the licensed cannabis-based treatment Sativex, to be available to people with MS on the NHS. You can get Sativex if you live in Wales but not elsewhere in the UK.
Sativex is expensive and people can’t afford to pay for it privately. This urgently needs to change. A legal change in November 2018 allowed specialist doctors to prescribe other cannabis-based products, only once all other treatments have been explored. We’re calling for Government to produce a clear plan aimed at making cannabis-based medicines more widely available for people with MS. Read about our campaigning on cannabis and MS
Treatment for secondary progressive MS
The first oral treatment for secondary progressive MS, siponimod, has been provisionally rejected for use on the NHS in England and Wales.
We’re working to change that decision.