You Are Not Alone! Contact Us.

Subscribe to our mailing list

* indicates required
SCN2A Groups
Email Format

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

Mail Donations To:

FamilieSCN2A Foundation, PO Box 82, E. Longmeadow, MA 01028

Don't miss important updates - SIGN UP FOR TEXT ALERTS

    Thank you for submitting

    Connect / Support / Research

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