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 16 results
Cystic Fibrosis Foundation
CFF is the world’s leader in the search for a cure for cystic fibrosis. Find information about CF, including treatment and research and how you can get involved.
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.
Cystic Fibrosis My Way: Managing Daily CF Care
In this series of videos, cystic fibrosis patients from The Children's Hospital of Philadelphia show how to properly perform some common CF therapies at home.
Scholarship and Grant Programs for Cystic Fibrosis Patients
Cystic fibrosis patients should consider this list of scholarship opportunities and grants. Look for one that might be a fit for you.
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.