MSA is a rare and progressive neurological disease that currently has no cure. We are the friends and family of Nick Yarsley who is living with this awful disease, Following the success of last years Yorkshire Three Peaks we are attempting Mount Snowdon this year to raise much needed funds and awareness of this disease MSA affects the brain cells needed for Movement, Speech, Swallowing and Continence The MSA Trust is the sole charity providing support to over 3,500 people affected by MSA in the UK and Ireland. The Trust provides support on all aspects of living with Multiple System Atrophy from symptom management, emotional support and advocacy to combating isolation. They receive no government funding; the MSA Trust is funded entirely by voluntary donations.