Jayant’s family traveled from Florida to Children’s Hospital of Philadelphia to seek the most experienced team for prenatal repair of spina bifida.

When doctors found bleeding on her unborn son’s brain, Sandrine turned to pediatric neurologists and fetal medicine experts at Children’s Hospital of Philadelphia.

Six years after prenatal repair of spina bifida, Will walks, runs and jumps, and continues to amaze his parents with all he can do.

Kathleen’s decision to travel from Florida to deliver her son in Philadelphia turned out to be a lifesaver when the cysts inside his CCAM ruptured at birth.

Diagnosed with a lymphatic leak before he was born, Austin is thriving today thanks to innovative treatment at Children's Hospital of Philadelphia.

Connor has been in the spotlight since before he was born. Doctors closed a hole in his spine while he was still in his mother's womb. Follow his journey.

Born with CDH, Gage made a full recovery after surgery at CHOP. To help others, his family is participating in research about long-term outcomes for CDH.

Read about 2-year-old Chelsea’s journey from prenatal diagnosis of gastroschisis, to surgery, recovery in the N/IICU, and clean bill of health.

Less than 24 hours after Madison was born, she had CDH repair surgery for a congenital diaphragmatic hernia. Now she’s in college with plans to become a doctor.

A family looks back on their child’s journey from a devastating prenatal diagnosis of sacrococcygeal teratoma, to hope