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We can now receive donations via text message! Simply text SCN2A or CURESCN2A to 443-21 and follow the secure link. Message & Data rates may apply. Donations can be made as one-time or reoccurring monthly. It's easy, quick and secure!

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 Donate using PayPal

"Families" is part of our name for a reason. Rare and devastating, SCN2A-related disorders (SRD) affect the entire family. Our team of leaders strive every day and in every way to improve the lives of not only the patients but the entire family.

Our MISSION is to accelerate research, build community and advocate to improve the lives of those affected by SCN2A-related disorders around the world.

The FamilieSCN2A Foundation believes research is our best hope for new treatments and eventually finding a cure for all SRDs. We are a registered 501(c)(3) organization and your donations are tax-deductible!

A cure for SRD can be a reality. However, the cost of finding a cure is expensive. Your donation can help save those suffering from the effects of SRDs. Every bit counts!

Donations can also be mailed to:

FAMILIESCN2A, PO Box 4260, Gettysburg, PA 17325.
FamilieSCN2A is a registered 501(c)(3) organization.

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Ways To Contribute

Whatever you decide, please let us know. We are here to support you with ideas, resources and more. Check out the FamilieSCN2A Fundraising Page on facebook to see how others have helped.


FUNdraising is not only about money, it also raises public awareness of SCN2A and the issues around rare diseases in general.

Raise Awareness

Share your story with friends and family, in private and/or through social media. Share our website with them.


Make a tax deductible donation directly to the FamileSCN2A Foundation to be used for raising awareness, research and supporting families

Raise Funds

Sign up with iGive, an automated program that donate a portion of online sales to charity.

Have a Party!

There are many direct sales vendors who would be happy to do a fundraiser for you.

Our goal is to find a cure!

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