Welcome to FamilieSCN2A
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.