MSA Trust

For people affected by MSA

This section aims to help you find out about the services, support and information that can help you to live with MSA.

Although everybody’s circumstances are individual, you will find that your needs, whether you are living with MSA, are a carer or family member, will change as life with MSA develops. Here you can find information to help guide you from being newly diagnosed through to treatment and management of MSA as life moves forward and needs evolve.

While we support anybody affected by MSA, by joining us (at no charge) you can make sure you are kept informed of latest developments around MSA, find out what’s happening in your area and access MSA Health Care Specialist support. To join us please click here.

We hope this section and our Living with MSA pages will answer any questions you have, but please contact us if you would like more information on any aspect of life with MSA that you need help with.

MSA Trust Webinars

The presentations below have been produced by the MSA Trust to provide information about MSA...

Living with MSA: The Emotional Impact

Living with Multiple System Atrophy (MSA) brings many challenges and just as with your physical...

Planning for the Future

Below you will find links to a number of pages that all contain information we...

Financial Support and Welfare Benefits

This section aims to help you find out more about the financial support and benefits...

For Young People

When someone in your family is diagnosed with Multiple System Atrophy (MSA) you may have...

Support for Children

‘My Special Activity book – all about multiple system atrophy’ is a resource created for...

Newly Diagnosed

If you have been newly diagnosed with MSA it can be hard to make sense...

Voice Banking – SpeakUnique

We are pleased to announce that we now offer funding for our members to access...