Top

24 Society

The 24 Society is made up of our most loyal supporters - monthly donors who choose to invest in steady, sustained progress for individuals and families affected by SCN2A-related disorders(SRD).

Join the 24 Society

What is 24 Society

Members of the 24 Society provide reliable, flexible support that allows the FamilieSCN2A Foundation to advance research, strengthen family programs, and maintain the infrastructure needed to move promising science toward treatments and cures. The number 24 reflects the SCN2A gene, located on chromosome 2 at position 24.3, and represents the ongoing commitment required to create real change in SRD research and care.

Monthly gifts help the FamilieSCN2A Foundation:

Sustain high-priority research initiatives

Support families throughout the year

Respond quickly to emerging opportunities

Plan responsibly for long-term impact

By giving monthly, you help keep momentum moving—month after month.

Make Your Monthly Gift

You can join the 24 Society with a $24 monthly gift, or by choosing a recurring amount that feels meaningful to you.

Join the 24 Society

Why Join the 24 Society?

A Sense of Purpose
As a monthly donor, you’ll know that progress is happening because of you—every month. Your continued support advances research, strengthens programs, and helps families feel supported.

Be Part of the Cure Every Month
Monthly giving allows you to contribute to steady, sustained progress, supporting awareness, families, and research efforts that move the field closer to treatments and cures.

Reduced Overhead Expenses
With automatic monthly payments, you add convenience and ease to your life while allowing more of your dollars to go directly to programs and services rather than overhead expenses.

Regular Updates
Through monthly giving, we know just how committed you are. You’ll receive ongoing information from the FamilieSCN2A Foundation on the latest activities of the organization, regular new stories from members of the SCN2A community, and more via email.

Special Recognition
Members of the 24 Society are graciously recognized in the FamilieSCN2A Foundation’s Annual Report and at the FamilieSCN2A Conference in appreciation of their long-term commitment.

Monthly gifts may be increased, adjusted, or paused at any time.

Join the 24 Society

The FamilieSCN2A Foundation is a registered 501(c)(3). FEIN 47-3169795
P.O. Box 4260
Gettysburg, PA 17325
info@scn2a.org

Contact us

Who are we?
The FamilieSCN2A Foundation was founded in 2015 by parents of children diagnosed with rare forms of epilepsy and autism as a result of a change in the SCN2A gene. The SCN2A gene helps regulate neuronal excitability, support brain development, and contribute to learning and memory. Changes in the SCN2A gene can cause a range of health issues known as SCN2A-related disorders (SRD). LEARN MORE.

Our mission is to accelerate research, build community, and advocate to improve the lives of ALL those affected by SCN2A-Related Disorders (SRD).

Subscribe & stay informed!

Newsletter sign-up

Quick links

What is SCN2A?

Newly Diagnosed

Global Support Group

Clinical Information

Registry

Clinical Trials

Get Involved

Awareness Day 2/24

Latest News

Key Publications

Resources

Shop the SCN2A store

One Wish. Made Possible by Many.

A child who can communicate. Fewer seizures. Greater independence. More good days. An effective treatment. A cure.

For families affected by SCN2A-related disorders, the wishes may look different, but ultimately, we share a wish for brighter futures.

Families, researchers, clinicians, advocates, and supporters are moving us forward. Every contribution matters, and every gift brings us closer to effective treatments and cures.

Be One of the Many. Give Today

The information provided on this website is not intended to diagnose or treat any disease or disorder. Full Disclaimer & Privacy Policy. Please direct any medical-related questions to your physician. © 2025 The FamilieSCN2A Foundation. Web Design by LMTD.