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Find an Organization by Health Topic Results: 1-15 of 15 Orgs
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AboutFace USA is a non-profit organization dedicated to providing information and emotional support to individuals with facial differences. Families are also included as part of the organization suppo... Details >
The American Cleft Palate-Craniofacial Association (ACPA) is an international, non-profit medical society of health care professionals from 30 disciplines and 40 countries who treat and/or research bi... Details >
Angioma Alliance is a non-profit international patient advocacy organization created by people affected by cavernous angioma (cerebral cavernous malformation). The organization works to inform and sup... Details >
The mission of the Children Craniofacial Association (CCA) is to improve the quality of life for facially disfigured individuals and their families. Nationally and internationally, CCA addresses the ... Details >
The Craniosynostosis And Positional Plagiocephaly Support, Inc. (CAPPS) is a non-profit organization dedicated to offering support and providing information to families who have a child with either Cr... Details >
The National Craniofacial Association, formerly the Debbie Fox Foundation, was created in 1969 to assist individuals with facial disfigurations and their families. The Association maintains a registr... Details >
The Foundation for Faces of Children (FFC) is a New England-based, non-profit organization, and a national source of information about craniofacial conditions. FFC is dedicated to improving the lives ... Details >
Let's Face It USA is a nonprofit network that links people with facial disfigurement and all who care for them to resources that can enrich their lives. The vision of Let's Face It USA is to educate t... Details >
The March of Dimes Birth Defects Foundation was established in 1938. Its mission is to improve the health of babies by preventing birth defects and infant mortality. The mission is carried out throu... Details >
Established in 1984, the Center provides diagnosis and treatment to children born with Birth Defects, Genetic Diseases and Mental Retardation. The Center consists of physicians and consultants in pedi... Details >
The National Foundation for Facial Reconstruction, formerly The Society for the Rehabilitation of the Facially Disfigured, was founded to help provide treatment and reconstructive surgery to facially ... Details >
Hemangioma Newsline became The National Organization of Vascular Anomalies in 2004 and is a non-profit organization established under IRS code 501c3a. The organization is dedicated to aiding individua... Details >
A private, not-for-profit volunteer medical services organization providing reconstructive surgery and related health care to indigent children and young adults in developing countries and the United ... Details >
This is an international charitable organization that provides support and informational resources for individuals affected by hemangiomas, port wine stains and other vascular birthmarks and tumors, a... Details >
This voluntary organization provides information and support for families of children with cleft lip and palate birth defects. The organization maintains a cleft lip and palate resource web site on th... Details >