Join me in supporting congenital heart defect research!
Thank you for visiting Team Ethan Wu’s fundraising page. This cause is very dear to our family and we appreciate all the support we can get!
Our family has been forever changed by the lasting impact of congenital heart defects (CHDs). In 2017, we learned that Ethan would be born with a congenital heart defect during my routine 19 week anatomy ultrasound. Ethan was born on May 18, 2017 with hypoplastic left heart syndrome and cor tri atriatum, 2 rare critical CHDs. Unfortunately, after enduring 3 open heart surgeries and living most of his life in a hospital, Ethan went home to heaven on November 16, 2017.
Please help us honor Ethan's memory, spread CHD awareness and raise money for much needed research to help other families like ours in the future. CHD research funding is not nearly where it needs to be. Together we can make a difference!
Watch us talk about why we fundraise for The Children's Heart Foundation: https://youtu.be/TD2-HXDg_Ac
Watch Ethan's Tribute video here: https://youtu.be/2rIhlsbz6as
Love, Elisa, Derek, Zoe and Naomi
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