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. Our vision is to find effective treatments and a cure for SCN2A disorders. Our mission is to improve the lives of those affected by SCN2A related disorders through clinical research, public awareness, early detection, patient advocacy, effective treatments, and family support. Our goal is to find a cure!
The FamilieSCN2A Foundation believes research is our best hope for new treatments and eventually finding a cure for SCN2A associated epilepsies. We are a registered 501(c)(3) organization, so you donations are tax deductible!
Your generous donations will go directly toward research, awareness, and to provide educational and emotional support for patients and families by connecting them with other families affected by SCN2A.
A cure for SCN2a can be a reality. However, the cost of finding a cure is expensive. Your donation can help save those suffering from the affects of SCN2A. Every bit counts!
Donations can also be mailed to: FAMILIEScn2a, P.O. Box 82, East Longmeadow, MA 01028
FamilieSCN2a is a registerd 501(c)(3) organization
*Photo courtesy Ra Design and Photography
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