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Providing research and information about relevant actions in relations
to SADS and related conditions is an important part of our work. We want to encourage genetic research in conditions that may lead
to sudden cardiac death in the young. Our role is as a link between
researchers and families. We also advocate for nondiscriminatory
treatment for people who are diagnosed with these conditions. SADS
is committed to supporting efforts that will improve the quality
of life for patients with heart rhythm abnormalities.
- Advocate for individuals struggling to find answers due to the
unexplained death of a loved one.
- Provide referral to and assistance with research projects.
- Work with other organizations-nationally and internationally-to
advocate for measures beneficial to families and patients (AEDs
in community, etc.)
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