CDH Stories
Quillan’s CDH Story
Quillan’s family learned about his congenital diaphragmatic hernia at their 21-week anatomy scan. Born nearly four weeks early, he needed immediate medical support and surgery at just 7 days old. After 56 days in the hospital, Quillan finally came home. Today, he is 2 years old, active, climbing, laughing, and thriving.
Grace’s Story - Congenital Diaphragmatic Hernia (CDH)
It was not an easy journey for our Amazing Gracie or our family, and it can still be challenging today. But we wouldn't trade our girl - exactly the way she is - for anything. Every day we're grateful for the gift of Grace.
Hayden’s Story - Congenital Diaphragmatic Hernia (CDH)
We still can't believe Hayden is doing as well as he is today. He has oxygen support at ¼ liter and does have a G-tube, but it seems pretty minor compared to what they were expecting for our little guy. He is both a miracle and a blessing, and we thank God every day that he proved everyone wrong.