You Can Unlock a Brighter Future for Children Living With
KCNT1-Related Disorders
Children with KCNT1-related epilepsy live with severe, often relentless seizures and complex medical needs. Families are frequently told there are few answers — and little hope.
The KCNT1 Epilepsy Foundation exists to change that.
Why your support matters
- Supporting families worldwide with trusted education and guidance
- Accelerating research that makes KCNT1 visible to scientists and industry
- Preparing families for clinical trials as new therapies emerge
You make it possible to accelerate KCNT1-specific treatment development and improve care worldwide.
Every contribution — large or small — is a meaningful step toward better treatments and a more hopeful future.
Thank you for being part of the KCNT1 community.
