SADS Foundation

Supporting families. Saving lives. 

The Sudden Arrhythmia Death Syndromes (SADS) Foundation is a global community of families, healthcare professionals, and advocates working to prevent sudden death due to genetic heart rhythm conditions.

Founded on December 12, 1991 by Dr. Michael Vincent, the SADS Foundation raises awareness, provides critical resources, and supports research and treatment for people affected by inherited arrhythmias—including Long QT Syndrome, Brugada Syndrome, CPVT, and ACM.

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🌍 Learn more: www.StopSADS.org

📧 Contact us: info@sads.org
📍 Based in the U.S., serving families worldwide