From support groups for teens, to physician-led webinars, medical education seminars, live Q&A with experts, an annual conference, and more, we provide programs to address: patient and family support services, physician and health professional education, public awareness, and advocacy & research.
SADS Foundation History
The SADS Foundation was founded by Dr. Michael Vincent on December 12, 1991. As a pioneer in the identification and treatment of Long QT Syndrome, Dr. Vincent convened the top global experts in electrophysiology with community members and supporters to begin the work we continue today.
Catch up on news from the SADS Foundation, including our latest newsletter and important updates for patients and families – like device recalls and new Drugs to Avoid for Long QT Syndrome
For members of the media: access press kit materials, including fact sheets, information on SADS conditions, and brochures. And learn more about the faces of SADS by reviewing published stories of SADS in the news.
Our mission is to help everyone equally, without any discriminating factors – no matter what SADS condition impacts the individuals and families. Learn about our commitment to diversity, equity, inclusion and belonging at the SADS Foundation