About The Gwendolyn Strong Foundation
Mission
The Gwendolyn Strong Foundation seeks to raise awareness about and fund research for Spinal Muscular Atrophy (SMA), the leading genetic killer of young children, and support those impacted by SMA and other life-altering diseases.
About
The Gwendolyn Strong Foundation (GSF) was born out of Bill and Victoria Strong’s firsthand experience with their precious daughter, Gwendolyn. Gwendolyn was born perfectly healthy in October 2007, but was diagnosed with the terminal disease Spinal Muscular Atrophy Type I at 6-months-old.
As witnesses to the degenerative cruelty of SMA, Bill and Victoria are personally and passionately dedicated to leaving no stone unturned in raising awareness about and funding research for SMA and supporting families who are impacted by SMA and other life-altering diseases.
