Home | myFace

OUR MISSION

myFace is a non-profit organization dedicated to transforming the lives of patients with facial disfigurement. With a special focus on children and their families, myFace funds medical, surgical, dental and psychosocial services as well as research and public awareness.
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There are many ways you can fundraise on our behalf to make an impact on urgently needed medical surgical & psychosocial care.
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Your support enables us to continue to provide comprehensive treatment to craniofacial patients in need.
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Start a student club, present myFace to your class, or develop a crowdfunding campaign. There are many ways to contribute greatly craniofacial patients.

TAKE ACTION

GET INVOLVED WITH OUR ACTIVE CAMPAIGNS

MYFACE EVENTS

UPCOMING EVENTS & GROUPS
UPCOMING EVENT
February 26, 2017 at 12:00 pm 333 East 30th Street, Lobby Office NEW YORK, NY

myFace WORKSHOPS

Join us for our next Sibling Workshop under the theme “Choose Kindness”

March 6, 2017 New York, NY

myFace PANEL LUNCHEON

March 16, 2017 New York, NY

YLB – A Night at The Gem

March 26, 2017 Brooklyn, NY

myFace Bowling Party

TESTIMONIALS

WHAT OTHERS ARE SAYING ABOUT MYFACE

myFace is the light in our long journey through darkness. For Hadi, it was a miracle. A smile so bright, nothing could wipe it off his face. For that, our whole family thanks myFace for all the joy they brought to us.

Rabah

myFace Parent

myFace has a loving and dedicated staff that directly help people throughout the journey of craniofacial reconstruction. Our family is forever grateful to their incredible support.

Lisa Pleasants-Smith

myFace Parent

I’ve never seen such an amazing organization. “myFace” is pure compassion, empathy, hope, and love.

Melanie Solis

myFace Parent

OUR LATEST GEAR

RAISE CRANIOFACIAL AWARENESS, IN STYLE

DO GOOD

BECOME A VOLUNTEER

Volunteer at an upcoming event or support group. You can help impact the craniofacial community by spreading awareness & becoming a myFace ambassador!

MYFACE NEWS

LATEST UPDATES AND PATIENT STORIES
EACH YEAR, AROUND
0
CHILDREN ARE BORN WITH A
CRANIOFACIAL CONDITION IN THE U.S.

Your support is extremely important and makes an immediate impact on urgently needed medical,
surgical and psychosocial services for all members of our craniofacial community.

NEWSLETTER SIGN-UP

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