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Welcome to the SADS Foundation. We hope this page will help you find the information you need about SADS conditions. Our Mission is to save the lives and support the families of children and young adults who are genetically predisposed to sudden death due to heart rhythm abnormalities. We provide education and support to families and the medical community who are dealing with these disorders. The SADS Foundation is dedicated to providing information, assistance, and hope. Facts about these Genetic Conditions:
What You Can Do:All children should have the Risk Assessment Form (PDF) completed—and be checked by a doctor if they answer “yes” to any question.
Warning Signs:
For More Information:
Physician Referrals:
These professional groups have information about physician specialists around the country:
SADS has a list of physicians that specialize in the electrical part of the heart and have experience with Long QT Syndrome. These are mostly pediatric electrophysiologists. We don't have physicians from all parts of the country on our list. We would be happy to answer any questions, send you materials or help direct you to the proper information. Just complete the Family Registration Form and we will get back to you as soon as possible. |