Feeding Your Baby with Cleft Palate
Information and advice about how to ensure proper nutrition and manage feeding difficulties that affect many babies with cleft lip and palate.
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Information and advice about how to ensure proper nutrition and manage feeding difficulties that affect many babies with cleft lip and palate.
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.
Omphalocele Awareness/Mothers of Omphaloceles (MOOS) is an Internet support group for families of children with omphaloceles.
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.
The American Society of Plastic Surgeons (ASPS) offers information about cleft lip and cleft palate repairs.
The Cleft Advocate educates and inspires families whose lives are touched by cleft lip and/or palate or other craniofacial anomalies.
AdoptCleft is a support group for parents wanting to adopt cleft children, parents that have cleft children (biological or adopted), and others that can contribute or learn from the conversations.
ACPA is an international nonprofit medical society of healthcare professionals who treat and/or perform research on birth defects of the head and face.
In this video, clinicians and patient families talk about the diagnosis and treatment of cleft lip and palate, the most common congenital facial anomaly.
CDH International is a nonprofit group that supports families and medical care providers of children with congenital diaphragmatic hernia.