SCN8A Epilepsy is a rare disorder that is known to affect less than 1,000 individuals worldwide. It can cause severe epilepsy, developmental delay, and other medical challenges.
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​The gene SCN8A was isolated in humans by Michael Hammer, PhD, a geneticist who found the gene in his own daughter, Shay, soon after her death in 2011.

​To honor Shay and all of those with SCN8A, The Cute Syndrome Foundation helped launch SCN8A Awareness Day on February 9th, Shay Hammer's birthday.

Visit our Youtube channel to view more SCN8A Awareness Day videos.

Visit the SCN8A Awareness Day website to learn more and find resources for spreading awareness.