Multiple Sclerosis (MS) Trust

MS is a cruel, life-long condition. It is most often diagnosed in young people in their twenties and thirties, just as they are making life choices about relationships, careers and having their own families. The impact of that diagnosis is terrifying. It can take away the ability to plan and can mean loss of independence, severe disability and isolation.

We don’t know what causes MS and as yet, there is no cure. It is endlessly variable and totally unpredictable – and people live with it for many years.

The MS Trust believes that with access to the right information and support, individuals and families affected by MS can live full and active lives. We provide:

- information that is tailored to what people want to know
- education for health professionals about what people with MS need
- research into better management of MS
- support for anyone affected by MS

The MS Trust would not be able to do its work without the generous support of individuals. Leaving a legacy to the MS Trust will enable us to support future generations affected by MS.