Supporting families. Saving lives.
The Sudden Arrhythmia Death Syndromes (SADS) Foundation is a global community of families, healthcare professionals, and advocates working to prevent sudden death due to genetic heart rhythm conditions.
Founded on December 12, 1991 by Dr. Michael Vincent, the SADS Foundation raises awareness, provides critical resources, and supports research and treatment for people affected by inherited arrhythmias—including Long QT Syndrome, Brugada Syndrome, CPVT, and ACM.
📺 Subscribe for expert webinars, patient stories, live Q&As, and the latest in SADS research and care.
🌍 Learn more: www.StopSADS.org
📧 Contact us: info@sads.org
📍 Based in the U.S., serving families worldwide
Shared 1 month ago
100 views
Shared 3 months ago
46 views
Shared 3 months ago
43 views
Shared 7 months ago
260 views
Shared 9 months ago
238 views
Shared 10 months ago
262 views
Shared 10 months ago
248 views
Shared 10 months ago
85 views
Shared 10 months ago
97 views
Shared 10 months ago
67 views
Shared 10 months ago
72 views
Shared 10 months ago
58 views
Shared 10 months ago
99 views
Shared 10 months ago
100 views
Shared 10 months ago
101 views
Shared 10 months ago
124 views
Shared 10 months ago
128 views
Shared 10 months ago
101 views
Shared 10 months ago
36 views
Shared 10 months ago
510 views
Shared 10 months ago
53 views
Shared 10 months ago
217 views
Shared 10 months ago
51 views
Shared 10 months ago
30 views
Shared 10 months ago
40 views
Shared 10 months ago
19 views
Shared 10 months ago
269 views
Shared 10 months ago
116 views
Shared 11 months ago
37 views
Shared 11 months ago
71 views
Shared 11 months ago
41 views
Shared 11 months ago
31 views
Shared 11 months ago
211 views
Shared 11 months ago
217 views
Shared 11 months ago
70 views
Shared 11 months ago
94 views
Shared 11 months ago
52 views
Shared 11 months ago
174 views