Don’t miss your last chance to donate by midnight on May 17 to our Match Grant Challenge and double your impact. But first, please read this special story from one of our cleft patients’ moms. It will inspire you, warm your heart, and show you the impact YOUR gift can have!
SPOTLIGHTS
Families in Crisis Need Your Help Today.
With the world turned upside down in just a few weeks, I need to ask you for your support. Many of the myFace craniofacial families have been hit hard by the COVID-19 crisis and are experiencing tremendous financial stress. Some have recently lost their jobs. Two-thirds of the families we
2nd Annual myFace Talent Show Brings the House Down!
On Sunday, March 1st, myFace hosted its 2nd Annual Talent Show – this year at Merkin Concert Hall in NYC. This show, made possible in part by generous support from The Warner Fund, provided a wonderful opportunity for a dozen of our myFace Stars – all impacted by craniofacial challenges
A Special Panel Discussion on Helping Parents to Advocate for Their School-Age Child
“Feed the attention of the child… Starve the attention of the bully…” – Lilliana Díaz-Pedrosa, Esq. Advocates for Children of NY Director, AFC Parent Center In January 2020, we held our first panel discussion on a very important topic: “Advocating for Your School-Age Children.” It was an invaluable program we put
It’s a new world… and myFace is always here for you.
Only a few short weeks after taking on the role of Executive Director with myFace in January, we find ourselves faced with an unprecedented pandemic. Each day we ask ourselves, “Where is the good in all this? How do we cope? When will it end?” We are deeply grateful to
Kyle’s Story
As told by Betsy, Kyles’s Mom: “Our son has a rare condition (we don’t like to use the word “disease”) called Nablus Syndrome. It is a micro deletion of the chromosome at 8q22 and is characterized as a mask-like facial appearance along with other distinct malformations of the body. As
Logan’s Story
As told by Leah, Logan’s Mom: “Logan as I named him was born with a bilateral cleft lip and aneterior palate. Ear pits. Anal stenosis. Oh and a very rare condition called microphthalmia / anophthalmia. This is the medical term for the absence of one or both eyes. Both the
Cameron Underwood – Face Transplant Patient
NYU Langone Health patient and myFace Star, Cameron, had a face transplant in January, under the leadership of Dr. Eduardo D Rodriguez, MD, DDS. myFace supported Cameron throughout this journey by providing travel and housing for his many trips back and forth between CA and NYC and more than 150
myFace Star: Gospel
Meet Gospel. Gospel is a beautiful, vibrant and determined 13-year-old – wise beyond her years. Her home is in Kingston, Jamaica, but she has spent the last couple of years in the US living with a host family so that she could undergo the special reconstructive surgeries she desperately needed
Actor Christopher Stadulis shares his inspirational story about defying odds & accomplishing his dreams
Hello, My name is Christopher Stadulis and I was born with a cleft lip and palate. Like so many of the kids that myFace helps, I know all too well the difficulty one can have growing up with a birth defect, disability or some sort of physical difference. Within the
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.