Congenital Diaphragmatic Hernia Support Groups & Links
Cherubs The association of CDH research, advocacy, and support. Information, forums, member blogs, and more.
March of Dimes Researchers, volunteers, educators, outreach workers and advocates working together to give all babies a fighting chance
Birth Defect Research for Children a parent networking service that connects families who have children with the same birth defects
Kids Health doctor-approved health information about children from before birth through adolescence
CDC - Birth Defects Dept. of Health & Human Services, Centers for Disease Control and Prevention
NIL - Office of Rare Diseases National Inst. of Health - Office of Rare Diseases
Analisa Amen
When Kristen Amen and Tony Garcia learned that their baby would be born with a condition called congenital diaphragmatic hernia (CDH), at first the news was devastating.
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