Join me in supporting congenital heart defect research!
Nicky was born September 6, 2016 with Tetralogy of Fallot with pulmonary atresia. He had his first surgery at 6 days old, and has 3 others since. He's had multiple cardiac catheterizations and hospital stays throughout his lifetime.
Nicky is so smart and loving. He's energetic and continues to bring a smile to everyone's face. We will forever be amazed by his resilience and strength.
We are forever grateful to his team of doctors and nurses. Thanks to the research that continues to be done, we get to enjoy our little boy every day. Any donation, no matter how big or small, can help to make a positive impact in the lives of kids just like Nicky! These heart warriors deserve to live the best life possible.
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