У нас вы можете посмотреть бесплатно Hemifacial Microsomia: Meet Connor and Laura (5 of 9) или скачать в максимальном доступном качестве, видео которое было загружено на ютуб. Для загрузки выберите вариант из формы ниже:
Если кнопки скачивания не
загрузились
НАЖМИТЕ ЗДЕСЬ или обновите страницу
Если возникают проблемы со скачиванием видео, пожалуйста напишите в поддержку по адресу внизу
страницы.
Спасибо за использование сервиса ClipSaver.ru
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.