Why We’re Doing Ks for Kids
In honour of Indie Avalon, a beautiful girl who sadly lost her life due to a rare genetic disease called Infantile Nueroaxonal Dystrophy.
There is currently no treatment and no cure for INAD.
Indie was 9 years old.
Rest in peace Boo.
Did you know that
1 in 20 Aussie kids are born with a genetic disease or birth defect? That’s one in every classroom!
This August, we’re taking on the
Ks for Kids challenge - walking or running to raise funds for
Children’s Medical Research Institute, supporting scientists who are working today to find cures for tomorrow.
Your donation will help keep labs running, research advancing, and hope alive for kids who need it most.
Every step we take is for them. Your donation will help us go the distance and fund vital research!
In honour of Indie Avalon, a beautiful girl who sadly lost her life due to a rare genetic disease called Infantile Nueroaxonal Dystrophy.
There is currently no treatment and no cure for INAD.
Indie was 9 years old. Rest in peace Boo.
Did you know that 1 in 20 Aussie kids are born with a genetic disease or birth defect? That’s one in every classroom!
This August, we’re taking on the Ks for Kids challenge - walking or running to raise funds for Children’s Medical Research Institute, supporting scientists who are working today to find cures for tomorrow.
Your donation will help keep labs running, research advancing, and hope alive for kids who need it most.
Every step we take is for them. Your donation will help us go the distance and fund vital research!
Well done Rebecca ❤️