We are an organization created by parents of children diagnosed with rare forms of Epilepsy and Autism as a result of a change in the SCN2A gene. Our vision is to find effective treatments and a cure for SCN2A related disorders. Our mission is to improve the lives of those affected by SCN2A related disorders through research, public awareness, family support and patient advocacy. We are a registered 501(c)(3) organization run entirely by parent volunteers.
To improve the lives of those affected by SCN2A disorders through research & public awareness.