We bring together families, medical professionals, and researchers through programs and events to improve care and find cures for SCN2A-related disorders.
The FamilieSCN2A Foundation is dedicated to supporting groundbreaking research and advancing awareness for SCN2A-related disorders. From educational webinars and community outreach initiatives to our annual conference, programs and events are designed to provide valuable resources, create a supportive environment for those impacted by SCN2A-related disorders, and share information on important scientific developments.
To understand SCN2A-related disorders may require learning some new vocabulary and scientific concepts. This collection will help!
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