.jpg)
Kristen Groseclose's Fundraiser
Together We Drive Discovery
This August, help shape the future of Smith-Kingsmore Syndrome research
Join Our Journey to Find Treatments for Smith-Kingsmore Syndrome
Twenty-three years ago, our world turned upside down. Our son Jack was diagnosed with profound cognitive and developmental disabilities - and for years, we had no answers. But we never gave up hope.
In 2018, Jack was diagnosed with Smith-Kingsmore Syndrome (SKS), a rare genetic condition that causes seizures, developmental delays, and severe sleep disruption. That diagnosis brought clarity - and connected us with other determined families worldwide.
Together, we founded the Smith-Kingsmore Syndrome Foundation to fuel research and support others on this journey. Thanks to you, researchers have developed SKS-model fruit flies and mice to explore treatment possibilities.
Your donation powers the next step - bringing hope to families like ours.
Thank you for helping rewrite the future. Together We Drive Discovery!