We've hit an amazing £100,000 raised from all your donations in just 18 months, since the Manx MSA Trust was founded by Chris Blake in February 2016. All the hard efforts of all our supporters have made it possible.
The funds raised go towards our three key aims of the charity, (1) to provide a hub in the Isle of Man for MSA patients & families, (2) to raise awareness of MSA among both the public and the IOM medical profession and (3) support research to find an early diagnosis of MSA.
Thanks to all our supporters for their help in raising such a fantastic amount in such a short time.
Companies that have helped us so far:
 |
 |
 |
 |
 |
 |
 |
 |
 |
 |
 |
 |
 |
 |
 |
 |
 |
 |
 |
 |
 |
 |
 |
 |
 |
 |
 |
 |
 |
 |
 |
 |
 |
 |
 |
 |
 |
 |
 |
 |
 |
 |
 |
 |
 |
 |
 |
 |
 |
 |
 |
 |
 |
 |
 |
 |
 |
 |
 |
Multiple system atrophy (MSA) is a progressive neurological disorder that affects adult men and women. It is caused by degeneration or atrophy of nerve cells in several (or multiple) areas of the brain which can result in problems with movement, balance and autonomic functions of the body such as bladder and blood pressure control.
© 2015 Manx MSA Trust. All Rights Reserved.
