Find all needed information about Craniofacial Support Canada. Below you can see links where you can find everything you want to know about Craniofacial Support Canada.
Children's Craniofacial Association is a national, 501(c)3 nonprofit organization, headquartered in Dallas, Texas. Nationally and internationally, CCA addresses the medical, financial, psychosocial, emotional, and educational concerns relating to craniofacial conditions.
http://www.cleftsmile.org/international-resources/canada-resource-page/
Are you expecting a baby with a Craniofacial Difference? Come and Join our Family and Get Support, Ask Questions, Get Answers, Meet Families and Build Relationships for a Lifetime. We are here for you EVERY step of the WAY! Are you looking for a Cleft/Craniofacial Team in your area? Cleft/Craniofacial Team Listings in Canada; Health Department
https://www.cappskids.org/craniosynostosis-support/
Sometimes we all need a little extra support. Cappskids.org launched it’s model in 1999. Facebook did not exist and Google was just a baby in it’s beta phase. Internet was still dial-up, slow speed and often unreliable. Where did parents go when they thought something was wrong? Cappskids.org introduced a support page where families could […]
http://www.faces-cranio.org/craniofacial-centers.html
FACES makes no referrals to specific craniofacial reconstructive surgeons; however, as one of our services to you, we are providing this list of Craniofacial Teams across the country.This list is arranged by state, with those in Canada being at the end of the list. New centers are being established every year; therefore, this list does not include every one.
https://www.aboutface.ca/
Our mission is to promote and enhance the emotional and mental well-being of individuals with facial differences and their families through social and peer support, information, educational programs, and public awareness.
http://www.faces-cranio.org/resources.html
We provide financial support for non-medical expenses to patients traveling to a craniofacial center for treatment. Eligibility is based on financial and medical need. Resources include newsletters, information about craniofacial conditions, and networking opportunities. National Health Law Program. 1444 I Street NW, Suite 1105. Washington, DC ...
https://www.myface.org/the-myface-center/
myFace established and maintains The Newman Family Support Center, the most comprehensive psychosocial team in any U.S. craniofacial center. The team at Newman includes a Social Worker, Clinical Psychologist, Geneticist, Pediatric Nurse Practitioner, Speech Pathologist, Nutritionist, and Family Program Coordinator.
"SMILES" is a group of dedicated families who have developed a first-hand understanding of the needs of children with cleft lip, cleft palate, and craniofacial deformities. Through our personal sensitivity, energy, knowledge, and love we are dedicated to improve the lives of …
http://www.faces-cranio.org/Disord/NSCleft.htm
Cleft Lip and Palate. Download PDF information sheet. Back to Craniofacial Anomalies. What is Cleft Lip and Palate? Cleft lip (split of the upper lip) and cleft palate (split of the roof of the mouth) are the most common types of congenital facial difference. A unilateral cleft lip occurs on one side of the upper lip.
http://www.faces-cranio.org/Disord/Pfeiffer.htm
Headlines, Craniofacial Support 8 Footes Lane Frampton Cotterell Bristol BS36 2JQ UK Email: [email protected] website: www.headlines.org.uk This excellent international organization has a booklet on Pfeiffer Syndrome, as well as a support network of families dealing with this syndrome.
Need to find Craniofacial Support Canada information?
To find needed information please read the text beloow. If you need to know more you can click on the links to visit sites with more detailed data.
