myFace Star Nicholas Zollo wrote a piece for the Future of Personal Health, a Mediaplanet site focusing on health insights and news, patient stories, and the latest in diagnostic and treatment options. In his piece, Nicholos writes about his experience of living with a cleft lip and palate, and the
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myFace Star Ava Beeler was featured in the Future of Personal Health, a Mediaplanet site focusing on health insights and news, patient stories, and the latest in diagnostic and treatment options. In this article, Ava opens up about her experience living with Pfeiffer Syndrome and maintaining a positive outlook despite
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myFace Executive Director Stephanie Paul sat down with the Great.com Podcast to spread the word about the comprehensive work we do to support and uplift members of the craniofacial community. Read more about the interview here, listen to the podcast on your favorite platform, and/or
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Every year, myFace helps hundreds of children born with craniofacial disorders, and supports thousands of procedures and consultations. It can be incredibly difficult for everyone: the parents, the medical team, and of course, the children themselves. Meet Flossy, one of our myFace Heroes. Her bravery and resilience are an inspiration
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Every year, myFace helps hundreds of children born with craniofacial disorders, and supports thousands of procedures and consultations. It can be incredibly difficult for everyone: the parents, the medical team, and of course, the children themselves. Meet Jahzara, one of our myFace Heroes. Her bravery and resilience are an inspiration
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Meet Wyatt, a member of the myFace Community Meet Wyatt, one of our myFace Heroes. His bravery and resilience are an inspiration to us all! Wyatt, 13 At the time he was born, his was the widest cleft that the myFace Center’s Craniofacial Team at NYU Langone Health had seen
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See the full PRWeb Release Here MYFACE IN PARTNERSHIP WITH RANDOM HOUSE CHILDREN’S BOOKS CELEBRATES THE DECADE LONG IMPACT OF R.J. PALACIO’S WONDER ON THE CRANIOFACIAL COMMUNITY AND READERS WORLDWIDE New York, NY (February 14, 2022) — Over the past ten years, since its original publication on February 14, 2012,
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myFace launched a new monthly podcast in June 2021 hosted by Dina Zuckerberg, Director of Family Programs. The series – myFace, myStory: Voices from the Craniofacial Community – aims to inform and educate the general public about craniofacial differences and the issues that individuals and families of the community face;
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Kelly Vurinaris is an international, bestselling children’s book author. But first and foremost, she is mom to beautiful 6-year-old daughter, Zoe, who was born with Treacher Collins Syndrome, a rare craniofacial syndrome that affects the formation of the ears, eyelids, cheek bones, and jawbones. Because Zoe was also born with
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On August 10, 2021, myFace presented a free educational webinar as part of our Transforming Lives series focused on helping parents create the building blocks for a successful school year, home life, and social interactions for children with craniofacial diagnoses. Below are some of the questions posed during the live
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By making a donation to myFace, you enable us to continue our mission of providing quality comprehensive craniofacial care and support, as well as education and information that empower patients, families and the greater craniofacial community, enabling them to lead full and productive lives.
