MSA is a rare degenerative neurological disease that leads to premature death and affects around 3,000 people in the UK. There is no known cause or cure.
We are the UK’s main charity dedicated to providing support to all those affected by this disease, including specialist support nurses, support groups, and research into the cause of and, one day, cure for MSA. We receive no statutory funding whatsoever, relying entirely on the generosity of our supporters.
There are many ways of supporting our work, from donating in memory of a loved one, setting up regular giving, undertaking a sponsored event, setting up a tribute garden and more. You can find out how to help by clicking on the links to the left or by downloading our fundraising leaflet here.
With your support we can do more. Thank you.
We are regulated by the Charity Commission and proud to be a member of the Fundraising Standards Board, a self-regulatory scheme which works to ensure that organisations raising money for charity from the public do so honestly and properly. Read our Fundraising Promise here.