 Aubrey had the type two variant of the disease which unfortunately was incurable.Â
Sadly Aubrey passed away from this cruel disease at just 9 months of age in 2019.
It is our hope that in bringing awareness to genetic disorders like that of Gauchers Disease valuable funds will be raised to help research and hopefully develop cures in the future so other children and families don’t have to endure the suffering that a genetic disorder diagnosis delivers.
This August marks the sixth anniversary of Aubrey’s passing, so we are taking on the Ks for Kids challenge - walking/running 60km to raise funds for Children’s Medical Research Institute, supporting scientists who are working today to find cures for tomorrow all in honour of Aubrey.
Your donation will help keep labs running, research advancing, and hopes alive!Â
Every step we take is in honour of Aubrey. Your donation will help us go the distance and fund vital research!
Your donation will help keep labs running, research advancing, and hopes alive!Â
Every step we take is in honour of Aubrey. Your donation will help us go the distance and fund vital research!
Your donation has been doubled by our sponsors!