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 or

Mail Donations To:

FamilieSCN2A Foundation, PO Box 4260, Gettysburg, PA 17325

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    Did you or your child just receive a new diagnosis of SCN2A? If so, please know you are not alone!