Mariella's Congenital Cystic Adenomatoid Malformation (CCAM) Story
Before Mariella was born, doctors found a life-threatening cyst: a congenital cystic adenomatoid malformation. Her family turned to CHOP for lifesaving care.
Patient stories
CCAM/CPAM: Congenital Cystic Adenomatoid Malformation (Pulmonary Airway Malformation) Patient Stories
Combination Lung Mass: Emma’s Story
Kelly Heffernan felt lost when a mass was discovered on her unborn daughter’s right lung. Here, she shares the story of how she and Emma Grace found their way to CHOP.
Eli’s Story: A Dad Reflects on His Son’s CCAM Diagnosis
Before Eli was born, he was diagnosed with a congenital cystic adenomatoid malformation (CCAM), a large mass in his left lung. Eli’s dad, Matt, shares the story of his family’s journey to CHOP.
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.