After receiving a prenatal diagnosis of CDH, Laura and Nick turned to the expertise of CHOP’s fetal team.

This video follows one family’s journey from prenatal diagnosis of congenital diaphragmatic hernia (CDH) through delivery and CDH surgery to discharge home.

When Henry was prenatally diagnosed with spina bifida in the middle of the pandemic, his parents turned to CHOP’s fetal surgery team for help and hope.

After an unexpected prenatal diagnosis, Olly’s parents found comfort with the experienced team at CHOP’s Center for Fetal Diagnosis and Treatment.

Not many people can say they underwent fetal surgery during a pandemic, but Jasmin did it to give her daughter a better chance at a healthy life.

Tenlee was 3 days old when her family learned reconstructive surgery wouldn't be enough to save her life — she needed a new heart.

Eva’s parents came to CHOP from Central America so she could have fetal surgery for spina bifida with the world’s most experienced team.

Kian’s parents credit Children’s Hospital of Philadelphia for going above and beyond to support their entire family during their fetal surgery experience.

Michael, 5, is meeting all his developmental milestones after surgeries for a severe heart defect. He was closely monitored by the Cardiac Kids Developmental Follow-up Program at CHOP.

Meet Trey and Emmett: They’re both from Ohio, they both have spina bifida, and they both had fetal surgery at Children’s Hospital of Philadelphia.