In 2007, documentary filmmakers Lisamarie Costabile and Mark Larson followed Dr. Thomas Romo and the Little Baby Face Foundation as they treated Peyton Sherrill, a boy from Alabama who was born with microtia; he was born without his right ear.
The Little Baby Face Foundation is a New York City-based organization of surgeons and medical providers who volunteer their time and expertise to treat children from around the world born with facial birth defects. Dr. Thomas Romo, a renowned plastic surgeon, started the foundation in 2002.
This is the first half of Costabile and Larson's 20-documentary.
Can I have Dr. Address in details, please many thinks
sophearreal1 11 months ago
hey veryone that left positive comments thats my little brother we thank you just keep praying for him
ccs3rd 2 years ago
I love the little boy, he is sooo cute!!!
navywife1977 3 years ago
I wasn't born with it. I was born with NOTHING wrong with me, and i THANK GOD for that.
alecfrank21 3 years ago
wow there are alot of people with micrtrotia there should be like a web page or a chat room or something
hockychick1317 3 years ago
Hey, I have microtia too, but mine dont look like the ones on this video. Do yours? (I've never talked to anyone else with microtia, that's why I'm asking)
laluez 3 years ago
like 4 8" y?
sailrchix95 3 years ago
how tall r u sail95
2pc123 3 years ago
i have mocratia, and i had the surgery when i was 8, you should go to dr. brent in california, he is the #1 microtia surguan in the world.. im 14 now
marmarxox 3 years ago
omg i went 2 this doctor cus i have mictrotia. he told me i was too small 4 this surgery and he does it on kids who r like 5 and 6. im 13
sailrchix95 4 years ago