our story

Matt and Crista Webber were delighted to find out that they were expecting twins in 2015. Their excitement quickly turned into worry when their twin daughter, Zoey, was prenatally diagnosed with Hypoplastic Left Heart Syndrome. Nash and Zoey were born in December 2015 and Zoey underwent her first open heart surgery at 9 days old. She had her second open heart surgery at 9 months old and she is currently awaiting her third operation. Matt and Crista have consistently had a positive and hopeful outlook on life with Zoey's condition.  Approximately 1 in 100 babies are born with a heart defect in the United States each year; raising awareness is something that has become very important to the Webber family. Families often face life long challenges and successful treatment requires highly specialized care. Many children depend upon extensive financial resources both in and out of the hospital. It is our intent to ease some of the financial burden from families during their journey with congenital heart disease.