Our mission is to save the lives and support the families of children and adults who are genetically predisposed to sudden death due to heart rhythm abnormalities.
The Warning Signs.
Family history of unexpected, unexplained sudden death under age 40.
Fainting or seizure during exercise, excitement, or startle.
Consistent or unusual chest pain and/or shortness of breath during exercise.
Patient and Family Support Services.
The patient and family support program provides access to information, resources, research and support to patients’ and families’ who are dealing with genetic conditions that cause sudden cardiac death in the young or who have lost a loved one to sudden unexplained death.
Welcome to the SADS Foundation.
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.
Jazz Night For SADS
Join us as we celebrate our 30th Anniversary with an evening together in a magical garden full of music, food, drawing prizes, and great company as we raise funds to help families continue to live and thrive on their journey with a SADS condition!
Living with SADS Webinars
Join our top experts who will share their knowledge and advice on topics important to living and thriving with a SADS condition.
Annual Virtual Conference
This year we’re holding our third Virtual International Conference in mid-July 2022. Because it’s virtual, families like yours across the globe can watch global experts give presentations on the newest in research and treatment – plus, it gives you a chance to meet others with your condition, and form lifelong connections!
30 Years of The SADS Foundation
The SADS Foundation was established on December 12, 1991 by Dr. Vincent and several dedicated colleagues and LQTS family members for the purpose of helping to prevent sudden and unexpected cardiac death in children and in young adults. Read more about our history.
Sharing Your Stories
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. We welcome you to browse others’ stories and to contribute your own.
SADS Channel Stories
Members of the SADS community share their perspectives and experiences living with or parenting a child with a SADS condition.
Families share memories and legacies of their children, spouses, and loved ones who died from a heart arrhythmia condition.
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!
Join our email list to get the latest SADS related news and updates delivered to your inbox.
Show Your Support
Your support—no matter the size—powers life-saving research and medical education, patient advocacy, and awareness for SADS conditions.
There are many ways to support our community, including becoming a sustainer as a monthly donor, making a one-time gift, hosting an online or in-person fundraiser, donating to one of our honorary funds, or with your own creative idea!
Learn more about how you can save lives and strengthen our community through the various ways to give.