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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Showing 1 - 10 of 23 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.
CureHHT
Cure HHT has consistently been at the center of the national and global effort to advocate for patients and families, raise awareness of HHT, guide and fund critical research, create lasting collaborations and encourage scientists to work on new treatments.
HHT Guidelines
From the Annals of Internal Medicine, the Second International Guidelines for the Diagnosis and Management of Hereditary Hemorrhagic Telangiectasia.
HHT Nosebleed Treatment Options
This resource provides a view of the many treatment options for nosebleeds cause by Pediatric Hereditary Hemorrhagic Telangiectasia (HHT).
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.