In honor of Father’s Day, we want to recognize awesome fathers everywhere; in particular we would like to highlight Russel Newman, proud and dedicated father of Nathaniel. Nathaniel was born with Treacher Collins syndrome 12 years ago and has so far undergone 56 surgeries.
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The myFace Blog
Family Spotlight: The Pleasants-Smith Family
We are a family of five, with three terrific kids: McLaine, Jaimeson and Andy. McLaine is our 21-year-old college student. She was born without a facial difference. Our 18-year-old daughter, Jaimeson, was born with a severe expression of Treacher Collins Syndrome. Two years after Jaimeson was born, we adopted our
A life Changing Experience
The day after I was born, a geneticist was able to inform my parents that I had a rare congenital birth defect, though they were unsure how to proceed. The condition caused the bones of my skull, mid-face and spinal column to be malformed, causing a multitude of other medical problems.
9 Ways To Boost Your Child’s Self-Esteem
Every year, thousands of the children born with facial difference. Living with a craniofacial difference may create pressures and challenges that can affect one’s self-esteem. Here’s how you should know about these challenges so you can help empower your child to thrive in school. 1.Be prepared for transitions. Visit your
Why We Give
Several years ago, Nick O’Neill and Mary Valiante found themselves in the happy position of being able to increase their charitable donations. After researching myFace and the work the organization does, Nick and Mary felt myFace would fit perfectly with their desire to support patients in need of facial reconstruction.
A Father’s Reflection
I have a quick reflection about fatherhood and love that I’ve been meaning to write about for awhile. As a father one of the biggest things I learned about parenthood from my dad was to love and sacrifice. For different people those things manifest in an infinite number of ways.
Face-transplant recipient meets dead donor’s sister
myFace is honored to provide critical psychosocial services to Richard Lee Norris on an ongoing basis including speech therapy, nutritional support and psychological counseling. myFace additionally provides airline transportation and housing to Richard when he travels to NYC for his medical appointments. He has become an integral member of the
The Thing about Wonder
By: Eloise Diaries So I finally did it… I finally read Wonder. I just sat down on Sunday morning while Landon nuzzled next to me on the couch and read it. For years now, when folks hear about Landon’s syndrome, most people offer “have you heard about the book Wonder?!”.
Posada Delivers in Clutch
By: William Montgomery for Times Herald-Record NEWBURGH — A few hundred Yankees fans gathered at Orange County Choppers on Sunday to wait for an autograph and handshake from Jorge Posada. They brought bats and balls and posters. And it was all for a good cause. Posada was joined by his
Zen and the Art of Cleft Discovery Part 2
In my last piece, I wrote about the different feelings that we experience as parents after finding out our child will be born with a cleft. I mentioned that doing research and coming up with a plan was a crucial part of getting to that place where you can be
No matter how you give, your support has a direct and lasting impact.
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.
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