You Are Not Alone! Contact Us.
The FamilieSCN2A Foundation is 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. We are a registered 501(c)(3) organization.
Contact Our Support Group
If your child has an SCN2A mutation, and you would like to join our Community Discussion Group on Facebook, send an email to firstname.lastname@example.org