Our mission

Transforming the lives of children

Transformative reconstructive surgeries worldwide for anyone who qualifies.

Our mission

Transforming the lives of children

Transformative reconstructive surgeries worldwide for anyone who qualifies.

About us

Expert Care for Every Case

From single-surgery cases to multi-year treatment plans, we offer comprehensive care to all our patients, regardless of the complexity of their situation.

Our achievements

One in every 1,100 children are born with facial deformities like atresia, cleft lip/palate, facial paralysis, and microtia.

Despite the impact on the child’s health, treatment of facial birth defects is often not covered by Medicaid and other low-tier insurance plans in the United States. In many low and middle-income countries, care options are severely limited or nonexistent.

700

Surgeries performed since 2002

16+

Conditions treated since 2002

Our achievements

One in every 1,100 children are born with facial deformities like atresia, cleft lip/palate, facial paralysis, and microtia.

Despite the impact on the child’s health, treatment of facial birth defects is often not covered by Medicaid and other low-tier insurance plans in the United States. In many low and middle-income countries, care options are severely limited or nonexistent.

700

Surgeries performed since 2002

16+

Conditions treated since 2002

What we do

We’re here to help

Our dedicated team of surgeons donates countless hours of time and expertise to provide the best corrective surgery to children in need of care. The Foundation covers expenses associated with treatment and travel, at absolutely no cost to our patients or their families.

Innovation

Our medical team pioneers cutting-edge research and techniques.

Help us make miracles

You too can be a part of transforming the life of a child and their family.

Patient stories

Transforming Faces,
Building Futures.

Dylan’s Journey with Goldenhar Syndrome and Hemifacial Microsomia

Dylan from Virginia Beach arrived at our offices for the first time in 2023. Dylan, born with Goldenhar Syndrome and hemifacial microsomia with microtia, is so inspiring because he researched and sought out help on his own.


Goldenhar Syndrome, hemifacial microsomia with microtia

Condition

Virginia Beach

Patient Origin

Seng Ly’s Journey with Venous Malformation

We want to introduce you to this sweet 3 year old boy from Cambodia, Seng Ly. He has been on quite a journey, not only traveling to New York City for the first time, but also in completely transforming his health and his face.


Venous Malformation

Condition

Cambodia

Patient Origin

Reena Returns for Venous Malformation Treatment

Reena, age 11 from the Philippines, came back to us recently to continue her treatment for the venous malformation on her lower lip, chin, gum, and tongue. Reena flew to New York City with her father for the first time in 2017 to have her first surgery with the Little Baby Face Foundation, and has had several trips back since.


Venous Malformation

Condition

Philippines

Patient Origin

From our patient stories

“I felt alone and lost in a maze of medical jargon and treatment options until I found the Little Baby Face Foundation...”

“I felt alone and lost in a maze of medical jargon and treatment options until I found the Little Baby Face Foundation. Bjorn is now receiving the specialized care he needs to not just survive, but thrive. He now has full hearing in both ears and we are eternally grateful to the Foundation for their care.”
Vinola
Parent

Blog

Transforming Faces,
Building Futures.