I put together this video after we got home from Children's Hospital of Philadelphia. I thought you all might like to see it. The video explains our full journey from the second we found out about Ava's birth defect until recently. This little girl has been through so much in just two short years.
I also have another blog with all the videos I have made to help get the word out about Congenital Diaphragmatic Hernia. It is cdhawarenessvideos.blogspot.com Feel free to go and look around.