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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.
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.
Omphalocele Awareness/Mothers of Omphaloceles (MOOS) is an Internet support group for families of children with omphaloceles.
The Braden QD education module is designed to educate staff on different components of the new Braden QD scale and provide case scenarios to practice using the tool.
The American College of Allergy, Asthma & Immunology provides information and resources about allergies and asthma for patients and families.
CDH International is a nonprofit group that supports families and medical care providers of children with congenital diaphragmatic hernia.