Mission
Cure for Casey Inc. is dedicated to finding a cure for Spinal Muscular Atrophy SMA by funding ground breaking research and raising awareness. SMA is a rare genetic condition that leads to the progressive loss of motor neurons resulting in muscle weakness and atrophy often robbing children and adults of their ability to walk eat or even breathe on their own. The Corporation was created in honor of Casey Little an individual who was diagnosed with SMA 5 days after he was born. Determined to make a difference in his life and the lives of others Caseys parents organized the first annual Cure for Casey golf outing in Summer of 2024. The Corporation intends to continue annual golf outing along with other fundraising events.