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Hemifacial Microsomia: Meet Connor and Laura (5 of 9)

Connor and his mom, Laura, talk about growing up with a craniofacial condition and the care they've received at CHOP. For more, http://www.chop.edu/plasticsurgery. Connor was diagnosed with Goldenhar syndrome and hemifacial microsomia soon after he was born. His mom took him to Scott Bartlett, M.D., a pediatric plastic surgeon at The Children's Hospital of Philadelphia. Since then Connor has had a series of surgeries. With the support of his family and the team at CHOP, he's a thriving 12-year-old who travels to schools to talk to his peers about what it's like to be a kid with a craniofacial difference.

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