Move 4 Bella was established in 2021 by her family to honour the short life of Bella Margie Gwen Tuddenham.
Bella was born with Spinal Muscular Atrophy (SMA), a genetic condition affecting the nerves that control muscle movement. A true angel, born at 3.33pm on 28th April and went to heaven at 11.11am on 18th May 2021. Though her time here was short, Bella’s life has inspired a mission of hope and change.
Through the KIDS Foundation Move 4 Bella:

Ride 4 Bella, held in November each year, brings together enthusiastic Hot Temple cyclists to ride for 12 hours on stationary bikes in a large indoor purpose built facility.Learn more

SMA Awareness Month is the month of August, uniting communities to raise awareness for Spinal Muscular Atrophy
There are many ways to support the KIDS Foundation, each are important and critical to our ability to educate and empower young people.