For more than 12 years, the Sudden Arrhythmia Death Syndromes Foundation (SADS Foundation) has worked to save the lives and support the families of children and young people genetically predisposed to heart...
For more than 12 years, the Sudden Arrhythmia Death Syndromes Foundation (SADS Foundation) has worked to save the lives and support the families of children and young people genetically predisposed to heart rhythm abnormalities.
Each month staff hear from new families who have lost a child or loved one to SADS conditions like long QT syndrome, Brugada syndrome, and cardiomyopathies. These arrhythmias may show no symptoms and often leave no trace in an autopsy. When there are warning signs, they are:
Fainting or seizure during exercise, excitement, or startle; family history of unexpected, unexplained sudden death in the young; consistent or unusual chest pain and/or shortness of breath during exercise.
If diagnosed early, many of these conditions can be treated easily, saving lives.
The Foundation operates three programs: public awareness of SADS' warning signs, patient and family support, and medical professional education. More than 10,000 families use Foundation programs annually.
Thank you for considering a donation to the SADS Foundation today.
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