Steven Gill is coordinating a series of events designed to raise money for the MPS Society to honour his father Andrew who had Fabry disease.
Story
I am taking part in Steven Gill's #59events for The MPS Society to help raise awareness of MPS, Fabry and related diseases. These diseases are rare genetic diseases which can cause a range of issues throughout a person's lifetime. By raising funds and awareness we are helping others affected by these little known diseases.
Share this story
Help Ronald Willett
Sharing this page with your friends could help raise up to 3x more in donations
The MPS Society provides specialist support to children, adults and families in the UK who are affected by MPS, Fabry and related lysosomal storage diseases and we fund research into treatment and therapies. These diseases are rare, genetic, life-limiting conditions with no cure.