The Sads Foundation
Founded in 1991 by Dr. Michael Vincent, The SADS Foundation is a national nonprofit dedicated to saving lives and supporting families affected by genetic heart rhythm conditions that can lead to sudden cardiac death. We bring together a powerful community of survivors, families, medical professionals, and researchers to advance early diagnosis, treatment, and public awareness of conditions like Long QT Syndrome, Brugada Syndrome, Arrhythmogenic Cardiomyopathy, and CPVT. Through education, advocacy, and family support programs, we work to ensure that no one faces a SADS diagnosis alone—and that more lives are saved every day. Based in Salt Lake City, UT | info@sads.org
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Decision-makers and verified team members
15 contacts with verified email or phone · masked until revealed.
- ME
Marcia e Baker
Program Director · General Business & Management
EmailPhone - CT
Chelsey Tufts
Awareness and Outreach Coordinator · Advertising & Marketing
EmailPhone - EW
Erin Waite
Technology and Administrative Coordinator · Other
EmailPhone - AL
Alice Lara
President & CEO · General Business & Management
EmailPhone - AH
Allie Hoth
Communications & Awareness Coordinator · Other
EmailPhone - KW
Ken Woodhouse
Director of Philanthropy and Partnerships · Other
EmailPhone
Showing 6 of 15 verified contacts
Top roles at The Sads Foundation
14 distinct titles indexed · top 10 shown.
- 2family support, advocacy & research director
- 1awareness and outreach coordinator
- 1communications & awareness coordinator
- 1comptable
- 1director of communications
- 1director of philanthropy and partnerships
- 1family support specialist coordinator
- 1president & ceo
- 1program director
- 1project manager
- +4more titles
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