Did you know...

• The most common birth defects in the US is Cleft lip and/or palate--1 in 600 babies.


• The Cleft Palate Foundation can refer you to interdisciplinary diagnostic and evaluations teams in your area


• There is a place you can go on the web which offers comprehensive information and support resources for families affected by the birth of a child with a cleft lip and/or palate

I recently met with some wonderful, dedicated people who provide information and support to families with children born with a cleft lip and/or palate. They work tirelessly to provide the most current information, resources and services available. The Foundation's mission, "To enhance the quality of life for
individuals affected by cleft lip and palate and other craniofacial
birth defects" is carried out by providing resources which focus on
topics such as "Feeding Your Baby," and listings by state of Cleft
Palate and Craniofacial diagnostic and evaluation interdisciplinary
teams. The website, www.cleftline.org, has information for both families and health care professionals and the helpline--1.800.24.CLEFT--provides callers with local support group resources. Check out the website and find answers to questions from the folks who care and are the recommended source for cleft lip and or palate information.