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When their unborn baby was diagnosed with congenital diaphragmatic hernia (CDH), Alyssa and Louis turned to CHOP for treatment before and after birth.
Lucy was born with small lungs and critical breathing challenges. The care she received at CHOP prepared her to go home with minimal breathing support.
After receiving a prenatal diagnosis of CDH, Laura and Nick turned to the expertise of CHOP’s fetal team.
After an unexpected prenatal diagnosis, Olly’s parents found comfort with the experienced team at CHOP’s Center for Fetal Diagnosis and Treatment.
After a long journey to overcome giant omphalocele, a life-threatening birth defect, Emma is thriving.
Elijah needed a lifesaving surgery while he was still in his mother’s womb. Today, he's an active 6-year-old who loves basketball and T-ball, goes swimming, rides his bike, and rock climbs.
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.
Even though home is near Washington, DC, Carter, 6, travels to Philadelphia for ongoing care for the congenital diaphragmatic hernia he was born with.
When Jameson was diagnosed with giant omphalocele before birth, the positive attitude of the team at CHOP made his parents feel much better about the journey ahead.
Upon learning their unborn child had CDH, the Porosoff family traveled from Florida for care at CHOP's Center for Fetal Diagnosis & Treatment.