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The Little Baby Face Foundation: Part 1 of 2

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Uploaded by on Jan 20, 2008

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.

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  • Can I have Dr. Address in details, please many thinks

  • hey veryone that left positive comments thats my little brother we thank you just keep praying for him

  • I love the little boy, he is sooo cute!!!

  • I wasn't born with it. I was born with NOTHING wrong with me, and i THANK GOD for that.

  • wow there are alot of people with micrtrotia there should be like a web page or a chat room or something

  • 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)

  • like 4 8" y?

  • how tall r u sail95

  • 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

  • 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

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