Books to Support Parents and Partners on the Postpartum Journey
This selection of books can help with many common feelings and emotions that parents and partners might feel before and after a new baby is born.
Our Richard D. Wood Jr. Center for Fetal Diagnosis and Treatment experts have created this list of resources to help you keep your child safe and well.
This selection of books can help with many common feelings and emotions that parents and partners might feel before and after a new baby is born.
CDH International is a nonprofit group that supports families and medical care providers of children with congenital diaphragmatic hernia.
Congenital diaphragmatic hernia (CDH) is just as common as cystic fibrosis, but many people have never heard of it. Get the facts about CDH and share to help raise awareness of the condition.
In this video, clinicians and patient families talk about the diagnosis and treatment of cleft lip and palate, the most common congenital facial anomaly.
Did you know that spina bifida is the most common permanently disabling birth defect in the U.S.? Learn more spina bifida facts and help spread the word.
Get the facts about twin-twin transfusion syndrome then share this infographic with your friends and family to help raise awareness of the condition.
Get the facts about fetal surgery then share this infographic with your friends and family to help raise awareness of the ways babies can be treated for serious and life-threatening conditions even before they’re born.
Find comprehensive breastfeeding information, online forums and support groups, FAQs, conferences, an international online store, and more.
March of Dimes is an international organization that works to prevent birth defects, premature birth, and infant mortality and to support expectant and new parents.
Omphalocele Awareness/Mothers of Omphaloceles (MOOS) is an Internet support group for families of children with omphaloceles.