| QUICK LINKS |
| ABOUT US |
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Sudden Arrhythmia Death Syndromes (SADS) Foundation was established on December 12, 1991 by G. Michael Vincent, M.D. and several dedicated
co-founders.
Our Mission is to save the lives of children and young adults who
are genetically predisposed or otherwise susceptible to sudden death
due to cardiac arrhythmias and to 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 & hope.
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Networking Support Program
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We are happy to announce the re-introduction of our Networking Program. Now, simply by enrolling and obtaining a username, you will be able to contact others in your geographical area and/or in similar circumstances. Support it is something that everyone needs, especially when dealing with health concerns: living with a cardiac arrhythmia and/or the sudden loss of a loved one due to a cardiac arrhythmia. This program was designed to facilitate emotional support and communication, about everything from helping re-direct a sports fanatic teen to dealing with ambivalent physicians. This program enables individuals with similar concerns and circumstances to communicate with each other. To join, click the link below and fill out the enrollment form. Once you receive your password, it is up to you to initiate communication with any or all of the others. SADS does not guarantee the willingness of anyone to communicate. There is no fee to enroll in this program, however, SADS is not responsible for the costs that occur as a result of communication. If interested, click
here. |