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.
Caring for your child
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Showing 1 - 10 of 19 results
March of Dimes
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.
Crisis Resources
View a variety of help hotlines, as well as websites available for families in need.
American Society of Plastic Surgeons (ASPS)
The American Society of Plastic Surgeons (ASPS) offers information about cleft lip and cleft palate repairs.
Cleft Advocate
The Cleft Advocate educates and inspires families whose lives are touched by cleft lip and/or palate or other craniofacial anomalies.
AdoptCleft
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.
American Cleft Palate-Craniofacial Association (ACPA)
ACPA is an international nonprofit medical society of healthcare professionals who treat and/or perform research on birth defects of the head and face.
Diagnosis and Treatment of Cleft Lip and Palate
In this video, clinicians and patient families talk about the diagnosis and treatment of cleft lip and palate, the most common congenital facial anomaly.
Undiagnosed Diseases Network (UDN)
Research program funded by the National Institute of Health (NIH). Some patients seen in the CHOP UDP are eligible and will also be asked if they want to enroll in the research side. You can visit their website to learn more about the research they conduct. Adult patients may be seen by the UDN site at Penn.
National Organization for Rare Disorders (NORD)
An educational link for organizations and individuals concerned with a rare disorder. They monitor legislation, research diseases, award grants and network individuals.