Multiple system atrophy (MSA) is a rare neurological disease with no known cause or cure.

Our dear friend Richard lives with this degenerative condition with his wife Ann and three children, Wolfie, Hannah and Henry. MSA results in problems and deterioration of multiple bodily functions such as speech, movement, balance, continence and blood pressure control. All of which have a catastrophic affect on everyday living.

MSA Trust's mission is to find the cause and, ultimately, cure for MSA. It also has a small grants scheme used to help support people living with this condition. These grants provide a varied range of support, from help towards purchasing mobility equipment, to respite care and counselling. However, the Trust can only afford to provide a very limited number of grants each year.

We are excited and looking forward to holding the 'Big Wig Ball - from Burlesque to Bugsy Malone' to raise funds so more families affected by MSA can be helped.

Please support us and thanking you in anticipation.