EAST SETAUKET - A 2-year-old girl from Ecuador who was born with a rare facial deformity is undergoing life-changing surgery here on Long Island. Angie Barreto had a birth defect that left her very disfigured, and back in Ecuador, her family didn't think anything could be done. But Blanca's House, a nonprofit group that provides free medical care, brought Angie to Long Island for help.
6 г. назад
a small montage of Eli's first year! Music written and performed by Morgan Andersen
3 мес. назад
Tres was born with Diprosopus, which is Greek for "Two Faces". He may look different on the outside, but Tres still likes to make friends just like most people. Follow Tres on IG at https://www.instagram.com/diprosopusdiaries/. SBSK's Socials: https://www.instagram.com/specialbooksbyspecialkids https://twitter.com/chrisulmer https://www.facebook.com/specialbooksbyspecialkids
4 г. назад
Violet Pietrok was born with a Tessier Cleft, a rare defect that left a fissure in her skull. Surgeons at Boston Children’s Hospital, aided by 3-D prints of her skull, hope to repair the damage. Produced by: Kassie Bracken Read the story here: http://nyti.ms/1D3MDQQ Subscribe to the Times Video newsletter for free and get a handpicked selection of the best videos from The New York Times every week: http://bit.ly/timesvideonewsletter Subscribe on YouTube: http://bit.ly/U8Ys7n Watch more videos at: http://nytimes.com/video --------------------------------------------------------------- Want more from The New York Times? Twitter: https://twitter.com/nytvideo Facebook: https://www.facebook.com/nytimes Google+: https://plus.google.com/+nytimes/ Whether it's reporting on conflicts abroad and political divisions at home, or covering the latest style trends and scientific developments, New York Times video journalists provide a revealing and unforgettable view of the world. It's all the news that's fit to watch. On YouTube. A New Face for Violet | The New York Times http://www.youtube.com/user/TheNewYorkTimes
8 мес. назад
Meet Kat. She's battling gastric cancer, but that hasn't stopped her passion for food. Watch her get an awesome surprise from her favorite restaurant. Tune in to the CW on May 25 to watch the newest season of My Last Days. Director JUSTIN BALDONI Producer SAGE PRICE Featuring KAT LAZO Created by JUSTIN BALDONI Executive Producers RAINN WILSON JUSTIN BALDONI SAM BALDONI AHMED MUSIOL FARHOUD MEYBODI Director of Photography JESSICA YOUNG Editor KEVIN FILIPPINI Hosted by JUSTIN BALDONI Composer JAMEY HEATH Post Production Producer REBECCA JAMESON Re-recording Mixer JOHN-THOMAS GRAVES Production Executives for SoulPancake SHABNAM MOGHARABI GOLRIZ LUCINA Production Coordinator ALEX ISOM Camera CODY SMITH TODD KELLSTEIN First AC & Camera Operator EMERSON BOERGADINE DIT ZACH WITHERSPOON Sound KYLE MCLANE PRODUCTION ASSISTANTS Janay Coplon Jacquline Fransway Caroline Grell Steven Ledezma Justin Madsen Kristen Stangas Moriah Stapf Joey Zeidan Post Production Geiger Post Sound Design and Mixing Services King SoundWorks, Inc. Special Thanks: Angenieux a Thales Group Brand Nissan North America, Inc EAT/Chef Natalie Young Hampton by Hilton FreeFly Systems Canon USA AbelCine On The Mark Media Charome Kaocharoen Amanda Slavin COPYRIGHT © MMXVI ALAMEDA PRODUCTIONS LLC. We love to connect with YOU, no matter what language you speak. Help SoulPancake create captions in your language by clicking here: http://bit.ly/27FqhGH ▃ ▅ ▆ SUBSCRIBE to SoulPancake ▆ ▅ ▃ http://bitly.com/SoulPancakeSubscribe THE SPOONFUL, our weekly dose of good stuff from across the web: http://ow.ly/t7K7p Buy our BOOK: http://book.soulpancake.com Follow us on FACEBOOK: http://facebook.com/soulpancake TWEET us at: http://twitter.com/soulpancake Visit our WEBSITE: http://soulpancake.com
5 г. назад
How surgeons at Riley Hospital for Children at IU Health are enabling Christian to achieve major milestones. Born with a rare facial defect--Tessier cleft--little Christian is one of only about 60 documented cases worldwide.
3 г. назад
CNN Newsroom live from LA Feb 05, 2016
5 г. назад
Before and after pictures of cinema star's teeth! See what improvements their teeth brought to them. Subscribe and like.
5 г. назад
On February 26, 2002, twins Kendra and Maliyah Herrin were born sharing a large intestine, bladder, liver and a single kidney. When they were 4 years old, their parents made the difficult decision to separate the twins—never before had doctors performed surgery on conjoined twins sharing the same kidney. Five months later, in 2005, these healthy girls traveled to Chicago to meet Oprah. Today, the twins are 11 years old. Watch to find out how they're doing and why they're no longer the only twins in their family. For more on #WhereAreTheyNow, visit http://www.wherearetheynow.buzz Find OWN on TV at http://www.oprah.com/FindOWN SUBSCRIBE: http://bit.ly/1vqD1PN Download the Watch OWN App: http://bit.ly/2hr1nX2 Download the OWN Bold Moves App: http://bit.ly/2hglOIa About Where Are They Now: Their stories made headlines across America. Now, the original series Oprah: Where Are They Now? tracks down the Oprah Show guests who made you laugh...and made you cry. Find out where they are now, plus see what happened to the biggest newsmakers of all time and how their lives changed after sudden fame and notoriety turned their worlds upside down. About OWN: Oprah Winfrey Network is the first and only network named for, and inspired by, a single iconic leader. Oprah Winfrey's heart and creative instincts inform the brand -- and the magnetism of the channel. Winfrey provides leadership in programming and attracts superstar talent to join her in primetime, building a global community of like-minded viewers and leading that community to connect on social media and beyond. OWN is a singular destination on cable. Depth with edge. Heart. Star power. Connection. And endless possibilities. Discover OWN TV: Find OWN on your TV!: http://bit.ly/1wJ0ugI Our Fantastic Lineup: http://bit.ly/1qMi2jE Connect with OWN Online: Visit the OWN WEBSITE: http://bit.ly/1qMi2jE Like OWN on FACEBOOK: http://on.fb.me/1AXYujp Follow OWN on TWITTER: http://bit.ly/1sJin8Y Follow OWN on INSTAGRAM: http://bit.ly/LnqzMz Follow OWN on PINTEREST: http://bit.ly/2dvfPeN How the Conjoined Herrin Twins Are Doing Today | Where Are They Now | Oprah Winfrey Network http://www.youtube.com/user/OWN
3 г. назад
Follow us on Instagram: https://www.instagram.com/isaiahs_journey2015/ Isaiah had gotten off the city bus and was crossing the road when he got hit by a truck. He was airlifted to Sunnybrook Health Sciences Center. As soon as he got there he had his spleen removed. He spent the next 3 weeks in a coma. He had many injuries that include Shattered cheekbone, fractured orbital bone, shattered gums, broken jaws, fractured ribs, punctured lung, broken arm and a severe TBI. The excellent team at Sunnybrook saved his life. He spent the next 2 months recovering. Doctors did not give Isaiah very good odds. He was not moving his left side, talkin or even really communicating. He would give the thumbs up and thumbs down but it was not consistent. All he could really do was lay in bed. He was sent to Holland Bloorview Kids Rehabilitation Center November 26th 2015 where I believe his true recovery started. The first day there he rolled over for the first time and by the end of that week he gave us his first smile. I could not praise the staff enough for how amazing they all were. After Christmas it was like a spark happened with Isaiah. He said his first word December 28th and a week later he was speaking full sentences. He started moving his left side New Years Eve and a week later he was moving his own foot to take a step. He was a totally different kid. He is a very strong and determined guy. He worked so hard and pushed through even on the painful days. My son is pretty incredible. First song: Hallelujah by Imogen heap Second song: Life of Riley Kevin MacLeod (incompetech.com) Licensed under Creative Commons: By Attribution 3.0 License http://creativecommons.org/licenses/by/3.0/
4 г. назад
A new dad with a severe facial disfigurement has defended his decision to have a baby daughter with the same condition. Simon Moore, 30, who's also profoundly deaf, has always been bullied and would hide indoors to avoid the stares of strangers. His life changed when his hearing dog Foggy, introduced him to Vicky, 36, at a sign language class five years ago and the pair married in 2012. The wanted a family so started IVF and made the decision to keep baby Alice when tests showed she also had the condition known as Treacher Collins Syndrome (TC). They had been offered a special IVF process which included state-of-the-art preimplantation genetic diagnosis to screen for the TC gene that Simon carried. The treatment would search for and destroy any embryos that carried the faulty gene.
3 мес. назад
Sophia is a 9 year old girl who likes to make new friends. She is diagnosed with Rett syndrome and lives with a facial deformity. Sophia hopes others will understand that inside she is just like everyone else. Follow Sophia's family on Twitter at https://twitter.com/Nataliew1020. SBSK's Socials: https://www.instagram.com/specialbooksbyspecialkids https://twitter.com/chrisulmer https://www.facebook.com/specialbooksbyspecialkids