After being prenatally diagnosed with congenital diaphragmatic hernia (CDH), Parker, now 9, was treated with extracorporeal membrane oxygenation (ECMO) on her first day of life.

After a year of intensive treatment, 14-month-old Evan Stickle is finally home. His family credits his turnaround to CHOP’s Newborn and Infant Chronic Lung Disease Program.

Five months pregnant with twins, Kim Hebron and her husband Vaughn learned their babies had a life-threatening condition called twin-twin transfusion syndrome (TTTS).

Rowan was diagnosed before birth with a sacrococcygeal teratoma (SCT), a tumor located on her tailbone. She underwent surgery at CHOP the day after she was born.

Khloe was just 2 days old when doctors noticed she was having digestive problems. She was transferred to CHOP where doctors discovered she had Hirschsprung’s disease.

Diagnosed with a severe congenital diaphragmatic hernia (CDH), Emerson’s family turned to CHOP, where an expert, multidisciplinary team made all the difference.

Hundreds of gravely ill newborns have benefits from EMCO, a machine that temporarily acts as the baby's heart and lungs, since 1990 when Katelyn became CHOP's first ECMO patient.

Diagnosed prenatally with the abdominal wall defect gastroschisis, Vincenzo’s family traveled to CHOP for delivery and expert surgical repair. See how he's doing 10 years later.

Born prematurely and with substantial hearing loss, Anna received a cochlear implant at CHOP — opening her world to language.

Brianna Malloy was diagnosed with gastroschisis, a type of abdominal wall defect, before she was born. She underwent successful repair surgery at CHOP.