The SADS Foundation is dedicated to raising awareness about sudden arrhythmia death syndromes (SADS), including Long QT Syndrome, Brugada Syndrome, and other heart rhythm disorders that can lead to sudden cardiac death in otherwise healthy individuals.
Our mission is to save lives through education, support, and advocacy while providing resources for patients, families, and healthcare professionals.
Connect with families who share a similar experience, give back, or help drive change around medical research, legislation, or awareness-building. Join us in making an impact!
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We provide comprehensive educational materials and awareness campaigns to help families and healthcare providers recognize and understand SADS conditions.
Our support network connects families affected by SADS, providing emotional support, resources, and community.
We fund critical research to advance understanding and treatment of sudden cardiac arrhythmias.
Your donation helps us continue our vital work supporting families and funding research.
Donate NowHave questions or need support? Reach out to us.