We're sitting and waiting in the prep room. Zoe's doc came in and announced there may be an emergency "case" which will take precedence. They may push her cath back, or reschedule it. Let's hope they tell us soon, since Zoe is STILL starving. Luckily she's sleeping in daddy's arms right now and is content. Will update when we get word.
On May 11, 2010, our family grew from three to four. Our little miracle child, Zoe Madison, entered the world. She was born with a severe congenital heart defect, Hypoplastic Left Heart Syndrome. Fifteen hours after birth, Zoe underwent her first open heart surgery. Her second open heart surgery took place on September 14, 2010. And her final staged cardiac reconstruction in August of 2013. She has half a functioning heart, which was mended by Dr. Thomas Spray at the Children's Hospital of Philadelphia. Yes, we traveled over 2,000 miles to obtain the best possible care.
As small and young as she is, Zoe is the new foundation to our family. She gives us strength and reminds us, everyday, how precious life is.
Please join us and share in our journey. I'm certain Zoe will continue to inspire you, as she has us and hundreds of lives already.
Facing a New Diagnosis of HLHS? Click below to find HOPE!