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    ABOUT US

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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 site updated September 26, 2007

 
SADS Registration

If you would like to receive a free informative packet about sudden death and LQTS, register with us today. We use information about your condition (& your family's) to help us with the statistics about SADS conditions. We do not sell or give your personal contact information to any other organization.
We will also add you to our mailing list so you can receive the SADS Foundation's newsletter & eNews.


  Name: Date of Birth: / / (mm/dd/yyyy)

Address: (required)

 Gender: Male  Female
City: Phone:
State: ZIP: E-mail: Required
Country:    


Do you know anyone who has the Long QT Syndrome?
Yes  No
If yes, please fill out the information below for that person:

  Name: Date of Birth: / / (mm/dd/yyyy)
Address: Gender: Male  Female
City: Relationship to you:
State: ZIP:    
Country:    


Has your family or someone you know experienced the sudden death of a child or a young adult?
Yes  No
If yes, please fill out the information below for the person that died:

  Name: Date of Birth: / / (mm/dd/yyyy)
Relationship
to you: 		Date of Death: / / (mm/dd/yyyy)
    Gender: Male  Female


Would you like an information packet on the Long QT Syndrome mailed to you?
Yes  No

How did you hear about SADS?

 

If you have any comments, please enter them here:

 

IMPORTANT: The SADS Foundation is committed to the privacy of your personal information. The information you give us will be used only by us, and will not be shared, sold, or released. Only combined, non-identifying statistics will ever be made public.