Sudden Arrhythmia Death Syndrome Foundation

Mission

The Sudden Arrhythmia Death Syndromes (SADS) Foundation exists to save the lives and support the families of children and young adults who are genetically predisposed to sudden death due to heart rhythm abnormalities.

About

Established on December 12, 1991 by Dr. Michael Vincent, The SADS Foundation is a community of families, medical professionals, and supporters saving lives and advancing care for people with heart arrhythmia conditions that can lead to sudden death.

“SADS conditions are rare, but you are not alone. Here, you will find a community of understanding, support and guidance from others who are navigating life with a SADS condition.”