Before Mariella was born, doctors found a life-threatening cyst: a congenital cystic adenomatoid malformation. Her family turned to CHOP for lifesaving care.
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.
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.
Before he was even born, Max Nazzaro’s treatment for congenital cystic adenomatoid malformation (CCAM) began at The Children's Hospital of Philadelphia.
