At just one day old, Emily underwent surgery to remove a sacrococcygeal teratoma (SCT), a large tumor that had grown to be a third of her size by the time she was born.

Madeline, a healthy girl at 9, had a heart operation at CHOP at 5 days old. Her parents and grandfather donate to CHOP to fund research for cardiac care.

Lynne and Bill Garbose provided the lead gift to create the Garbose Family Special Delivery Unit (SDU) at CHOP, a specially created birthing suite for mothers carrying babies with known birth defects.

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.

Caila was diagnosed with hypoplastic left heart syndrome (HLHS) and treated at CHOP by the Cardiac Center team, which is at the forefront of diagnosing and treating HLHS.

After learning their baby had CDH, the Pappas family traveled from Tennessee to seek care at CHOP's Center for Fetal Diagnosis and Treatment in Philadelphia.

Diagnosed before birth with giant omphalocele, Charlotte came to CHOP for delivery, surgery and follow-up care by a team experienced in caring for this birth defect.

Casey and Bryan Kirsch were determined to give their son Jackson every chance to live a healthy life when they learned that he had a giant omphalocele.

Audrey Rose Oberio was prenatally diagnosed with myelomeningocele (MMC), the most severe form of spina bifida. She became CHOP's 1,000th fetal surgery patient.

Caoimhghin was diagnosed before birth with spina bifida, and was the very first baby delivered in the Garbose Family Special Delivery Unit at CHOP.