Food as Medicine: Anti-Inflammatory Diet
This resource from Children’s Hospital of Philadelphia (CHOP) how to eat a well-balanced diet that may decrease inflammation and promote overall health.
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Showing 1 - 10 of 33 results
Role of ECMO in Treating Babies with Congenital Diaphragmatic Hernia
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.
Frequently Asked Questions about Congenital Diaphragmatic Hernia: Helping You Make Choices About Your Child's Care
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.
IBD Child, Adolescent and Family Support Group
We welcome children, adolescents and families to join us to discuss their concerns and the emotional challenges of living with Crohn's disease and ulcerative colitis.
How to Administer High-volume Colonic Enemas
Learn how to administer high-volume colonic enemas from an expert at The Children's Hospital of Philadelphia.
How to Give an Enema to a Child
Learn how to administer a saline, mineral oil or Bisacodyl enema to a child. This video offers parents and caregivers step-by-step instructions.
How Anorectal Manometry Is Performed
In this video for parents and caregivers, you'll learn about prep instructions for an anorectal manometry exam, what to expect during the procedure and what your child will need to do during the test.
How Esophageal Manometry Is Performed
Esophageal manometry is a procedure that measures pressure, sensation and coordination of the esophageal muscles. In this video for parents and caregivers, you'll learn about what you and your child can expect during this procedure and watch as it's performed on a medical mannequin
National Organization for Rare Disorders (NORD)
The National Organization for Rare Disorders (NORD) provides advocacy, education and other services to improve the lives of all people affected by rare diseases.
Omphalocele Awareness/Mothers of Omphaloceles (MOOS)
Omphalocele Awareness/Mothers of Omphaloceles (MOOS) is an Internet support group for families of children with omphaloceles.