Find all needed information about Craniofacial Support. Below you can see links where you can find everything you want to know about Craniofacial Support.
https://headlines.org.uk/
Headlines Craniofacial Support. We are the leading UK charity supporting people with craniosynostosis and other rare craniofacial conditions. Craniosynostosis is a rare craniofacial condition where two or more plates of the skull prematurely fuse to each other, usually before birth. This results in the baby’s skull not growing properly and ...
https://pediatricfacialsurgery.org/
NextGenFace provides comprehensive, one stop, state of the art support to patients with craniofacial conditions and their families by helping them identify medical, surgical and psychosocial specialists to address their conditions. Watch the Film.
https://www.chop.edu/centers-programs/craniofacial-program
If your child has a complex craniofacial condition, our Craniofacial Program provides comprehensive, family-centered care from time of diagnosis through surgery and long-term care. Our multidisciplinary team of specialists has among the most experience in the country when it comes to caring for children with anomalies of the face and skull.
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.
https://www.nyp.org/pediatrics/services/craniofacial-centers/support-and-therapy-services
The care of young patients with craniofacial syndromes at NewYork-Presbyterian is provided in a family-centered environment by dedicated interdisciplinary teams of surgeons, pediatricians, dentists and other oral care specialists, nurses, audiologists, speech and language therapists, feeding therapists, occupational therapists, geneticists, social workers, and child life specialists.
http://www.craniofacial.ie/support-us/
Supporting staff attending national & international craniofacial meetings to enhance learning and expertise; If you would like to support the work of the National Paediatric Craniofacial Centre (NPCC), please contact. Noelle O’Mahony, Craniofacial Clinical Services Co-ordinator. OR. Linda Comey, Administrator, Craniofacial Services Team
https://www.barrowneuro.org/outreach/cleft-and-craniofacial-support-group/
The Barrow Cleft and Craniofacial Support Group provides support, peer advice, encouragement, and social engagement for people with cleft lip, cleft palate, and other craniofacial conditions.
https://www.childrens.com/specialties-services/specialty-centers-and-programs/plastic-craniofacial-surgery
"As soon as we met her surgeon, we knew she was in the best hands possible," Manuel says. James Seaward, M.D., plastic and craniofacial surgeon at Children’s Health and Assistant Professor of Pediatric Plastic and Craniofacial Surgery at UT Southwestern, met Manuel and his wife, Belinda, after an ultrasound revealed the cleft lip and palate.
https://health.ucdavis.edu/children/clinical_services/cleft_craniofacial/resources.html
The Cleft and Craniofacial Program has identified numerous support groups and organizations that can be helpful for pediatric patients with cleft and craniofacial problems.
https://www.craniofacial.com.au/
The Foundation, established some three decades ago, has throughout its history provided support and care for cranio-facial health services across the Women’s and Children’s Hospital and the Royal Adelaide Hospital, and to patients around the world. We continue to support patients of clinicians working at those hospitals. to this day.
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