Welcome to Vivian's Crew!
Thank you for visiting our fundraising page for the Virtual Congenital Heart Walk this year! Raising funds for CHD research is critically important to all Heart Warriors and Heart Angels, and personally very meaningful to our family.
Vivian was diagnosed with CHD in utero at 20 weeks. What started as Tetrology of Fallot with Pulmonary Atresia, ended as Tetrology of Fallot with Pulmonary Atresia and MAPCAS. As many know, Vivian has gone through two open heart surgeries. One of those surgeries the doctors found that the intervention they need to perform would not work because her anatomy was too extensive. We were sent to Stanford for a full heart repair in which Vivian underwent an 18 hour surgery.
She has beat odds and is stronger than ever. We adore watching out little girl thrive and grow. But we know none of this would be possible without our immense support of doctors, therapists, and surgeons. We owe it to them that Vivian is in perfect condition. Without foundations like The Children’s Heart Foundation, our doctors and researchers wouldn’t have the means to have to the knowledge they currently do about CHD.
As Vivian’s Crew, we continue to raise awareness and fundraise to help additional families that are also in our shoes.
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