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 email@example.com
Make Donation Online
Support Our Cause At iGive.com
Over 1,700 stores will give a percentage of the sales directly to The FamilieSCN2A Foundation to further our research.
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Did you or your child just receive a new diagnosis of SCN2A? If so, please know you are not alone! CLICK HERE