The FamilieSCN2A Foundation is a registered 501(c)(3).
FEIN 47-3169795
P.O. Box 4260
Gettysburg, PA 17325
info@scn2a.org
Who are we?
The FamilieSCN2A Foundation was founded in 2015 by parents of children diagnosed with rare forms of epilepsy and autism as a result of a change in the SCN2A gene. The SCN2A gene helps regulate neuronal excitability, support brain development, and contribute to learning and memory. Changes in the SCN2A gene can cause a range of health issues known as SCN2A-related disorders (SRD). LEARN MORE.
Our mission is to accelerate research, build community, and advocate to improve the lives of ALL those affected by SCN2A-Related Disorders (SRD).
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The information provided on this website is not intended to diagnose or treat any disease or disorder. Full Disclaimer & Privacy Policy. Please direct any medical-related questions to your physician. © 2025 The FamilieSCN2A Foundation. Web Design by LMTD.