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

When Alicia and Matthew learned their unborn baby had spina bifida, the prognosis was grim. But the team at CHOP offered them hope through fetal surgery. See how she's doing 3 years later.

The CHOP care team helped Janessa and Matt prepare for the loss of one daughter, while finding joy in welcoming another.

A spina bifida diagnosis led Baylee and Louis to make the trip from their home in Florida to Children’s Hospital of Philadelphia for fetal surgery.

Before Mariella was born, doctors found a life-threatening cyst: a congenital cystic adenomatoid malformation. Her family turned to CHOP for lifesaving care.

Elliana and her mom, Nicole, traveled from Michigan to Philadelphia to have fetal surgery for myelomeningocele, the most serious form of spina bifida.

Identical twins Vale and Shea were diagnosed before birth with twin-twin transfusion syndrome (TTTS), and underwent fetoscopic laser ablation at CHOP.

After learning her unborn daughter, Avery, had spina bifida, Katie traveled from Maryland to have prenatal surgery at Children’s Hospital of Philadelphia.

Even though home was near Washington, DC, Carter, traveled to Philadelphia for ongoing care for the congenital diaphragmatic hernia he was born with.

The Watkins family traveled from Florida to Children’s Hospital of Philadelphia so that their unborn baby girl, Scout, could have fetal surgery for spina bifida.