Pulmonary Hypoplasia Program Patient Stories
11 - 17 of 17
Congenital Diaphragmatic Hernia: Milana’s Story
Upon learning their unborn child had CDH, the Porosoff family traveled from Florida for care at CHOP's Center for Fetal Diagnosis & Treatment.
Congenital Diaphragmatic Hernia: Wesley’s Story
When Wesley was diagnosed with a congenital diaphragmatic hernia, his family relocated from New York to Philadelphia to find the expert care he needed to survive.
Congenital Diaphragmatic Hernia (CDH): Laura's Story
Prenatally diagnosed with a severe congenital diaphragmatic hernia (CDH), Laura underwent successful CDH repair surgery at Children’s Hospital of Philadelphia.
Congenital Cystic Adenomatoid Malformation (CCAM): Max's Story
Before he was even born, Max Nazzaro’s treatment for congenital cystic adenomatoid malformation (CCAM) began at The Children's Hospital of Philadelphia.
Congenital Diaphragmatic Hernia: Peyton's Story
Peyton Laricks underwent successful surgery at Children's Hospital of Philadelphia to repair a prenatally diagnosed congenital diaphragmatic hernia (CDH).
Giant Omphalocele: Charlotte's Story
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.
Giant Omphalocele: Jackson's Story
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.
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