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Welcome to Our Web site!Our daughter was born with Ebstein’s Anomaly in 1996 and had her first surgery in May of 2007. After working with many of the top surgeons around the country, it’s clear that advances in new valves and new techniques in surgery will greatly improve the outcomes of kids and adults going forward. We will accomplish our goals by funding research to advance the diagnosis, treatment and prevention of this rare congenital defect. Each year, we fund the most promising research under the direction of our Advisory Board. Our advisor will be doctors and institutions who are dealing with Ebstein's cases as well as other congenital heart defects on a daily bases. Board Of Directors
Medical Advisory Board
Contact Us
The Ebstein’s Anomaly Foundation is a 501 (c) (3) tax-exempt charitable organization. We do not receive any government funding. Our success is because of the generosity and passion of our supporters.
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This site was last updated 05/01/08