Congenital Cystic Adenomatoid Malformation (CCAM) Surgery: Owen’s Story
The fetal medicine team at Children’s Hospital of Philadelphia made a treatment plan for his CCAM/CPAM, and Owen is now home and happy after surgery.
You will receive care from a highly skilled and compassionate team with a global reputation. This team helped shape modern fetal care and continues to improve techniques and treatments.
The fetal medicine team at Children’s Hospital of Philadelphia made a treatment plan for his CCAM/CPAM, and Owen is now home and happy after surgery.
Chris and Jolin traveled from their home in Pensacola, Florida to Children’s Hospital of Philadelphia to give their son, Max, access to world-class CDH care.
CDH can be a devastating diagnosis for an expecting parent to receive. But for a select group of babies with the most severe form of CDH, treatment before birth may help.
One family shares their experience for parents who learn their child has a severe diagnosis before birth
Born with a hole in her diaphragm (congenital diaphragmatic hernia), feeding difficulties were one of the biggest hurdles little Maggie has had to face in her CDH journey.
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.
When Jaxon’s family learned he had congenital diaphragmatic hernia, they traveled from West Virginia to seek care from the CDH experts in Philadelphia.