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Babies born with congenital diaphragmatic hernia (CDH) may go on ECMO if they aren’t responding well to other efforts to stabilize them. Find answers to common questions parents have about this potential treatment.
NSF is a patient-led nonprofit organization dedicated to helping children, parents, adults and healthcare providers to understand the complexities of spinal deformities.
Omphalocele Awareness/Mothers of Omphaloceles (MOOS) is an Internet support group for families of children with omphaloceles.
OrthoInfo is a trusted source of information from AAOS about musculoskeletal conditions and injuries — how they are treated, as well as how they can be prevented.
CDH International is a nonprofit group that supports families and medical care providers of children with congenital diaphragmatic hernia.
More information about congenital diaphragmatic hernia (CDH) to help make choices about your child’s care and choose a CDH treatment center that is right for you.