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There are plenty of ways to help the SADS Foundation’s mission to support families and save the lives of those affected by SADS conditions. Whether it is lending your voice, giving your time, planning a fund-raising event or sharing our story with others, your help is greatly needed and we look forward to working with you for years to come.
Fundraising Events
Working with a small staff and a nationwide team of volunteers, we educate physicians, patient families, and the general public about diagnosis and treatment of several life-threatening but treatable arrhythmias. By organizing events, volunteers raise a large part of the Foundation's operating funds each year. Across the United States they organize dinners, golf tournaments, jump-a-thons, and other events that simultaneously raise community awareness and critical funding. We endorse and support these grass roots efforts.
Please contact
Laura Wall
or call 800-786-7723 for advice, support and materials for your own fundraising idea to benefit SADS.
See
upcoming
fundraising events.
See a list of
past
fundraising events.
Click
here
for more information on how to get started with your own fundraising event.
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Help others by sharing your story.
Volunteer
The gift of time can provide a meaningful experience for you while helping others. Volunteers are vital to the work of the SADS Foundation. Your valuable skills and fresh perspectives will make a difference for people living with SADS.
Awareness
Raising awareness of SADS conditions is not only important but also SAVES LIVES! The SADS Foundation has a wide variety of opportunities for raising awareness, take a look and see what strikes your fancy. Contact
Adrienne Butterwick
or call 800-STOP-SAD to get involved with SADS awareness.
Sudden Death Response Plan
The SADS Foundation has an active outreach plan for when sudden death occurs in a community.
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Family history of unexpected, unexplained sudden death under age 40.
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