Thank you for your interest in supporting our SCN2A Warrior, Marty for The FamilieSCN2A Foundation a 501(c)(3) nonprofit—which helps over 2,500 families worldwide to raise critical funds for SCN2A research, advocacy, and family support. SCN2A is a gene we all have. When it’s changed, it can cause disease that may lead to severe, hard-to-treat epilepsy, developmental delays, movement disorders, and/or autism. Your support helps drive research towards treatments, patient assistance, family travel grants to attend conferences, sibling support, and meet-ups that build lifelong connections. Whether you choose to donate, join our team, or help spread the word about SCN2A disorders—you are making an impact,⚡️