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.
1 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
3 г. назад
CNN Newsroom live from LA Feb 05, 2016
8 г. назад
Chrissy Steltz' face was shot 11 years ago, now doctors have given her a new one. SUBSCRIBE for the latest news and updates from ABC News ► http://www.youtube.com/subscription_center?add_user=abcnews To read the full story and others, visit http://www.abcnews.com Watch more news stories from ABC News! More Nightline► https://www.youtube.com/watch?v=Dn3Ldv_mePs&list=PL31751769A1264A20 Similar headlines from ABC News► https://www.youtube.com/watch?v=IVGAI8o5i4o&list=PLQOa26lW-uI-OGtGrSH3xPaGciCMevaww For the past 11 years, Chrissy Steltz had been living without a face. After an accident with a shotgun destroyed her face and left her blind, Steltz made incredible strides toward living a normal life. She learned to read Braille and use a cane. She met her boyfriend in a school for the blind. And she gave birth to a son on July 23, 2009. --To read the full story and others, visit http://www.abcnews.com Follow ABC News across the web! Facebook: http://www.facebook.com/abcnews Twitter: http://twitter.com/ABC Instagram: https://instagram.com/ABCNews/ Watch as criminal investigations unfold, and witness the technology that helps the real life crime scene investigations (CSI) bring criminals to justice. Watch the stories of ordinary crime and the work of criminal masterminds. Advance through the justice system and the aftermath that follows a high profile investigation. From the start to finish ABC News is your source for the breaking stories of the rising crime rate in our nation. Stay informed on the latest crime news with abcnews.com. Nightline is a 30 minute late-night news program currently airing weeknights on ABC at 12:35am | 1:35am ET. Hosts Juju Chang, Dan Abrams and Dan Harris bring you in-depth reporting on the major stories, hot topics, and the day’s breaking news. You can catch Nightline every night just after Jimmy Kimmel Live! Make ABC News your daily news outlet for breaking national and world news, broadcast video coverage, and exclusive interviews that will help you stay up to date on the events shaping our world. ABC News’ show roster has both leaders in daily evening and morning programming. Kick start your weekday mornings with news updates from Good Morning America (GMA) and Sundays with This Week with George Stephanopoulos. Get your evening fix with 20/20, Nightline, and ABC World News Tonight with David Muir. Head to abc.go.com for programming schedule and more information on ABC News.
2 г. назад
R.I.P Cayden Wayne Quinlan...born on July 10th 2008 @ 2:32 am. 9 lb's & 21 inches long! Everyone wants to know why my son died only two days after his due date...?? %#@! And boy do I wish I had the satisfaction of knowing that 4 myself, but ONLY God knows that for now. What was supposed 2 be just another doctors appointment to check on my baby turned into THE worst day of my life! I had a totally normal & VERY healthy pregnancy. He was due July 7th! I went in for my routine weekly pre-natal check up on Wed-July 9th 2008, being just 2 days overdue & they couldnt find a HEARTBEAT! They sent me to the hospital to be induced, & in dis-belief of what I heard @ the Doctor's office, I kept HOPE alive 4 my BEAUTIFUL BABY BOY! I kept the same birth plan in place 4 him & I. And I labored & delivered NATURALLY with NO drugs. I just wanted to get him out as quickly as possible in hopes that we could revive him if needed! I asked if they could do a C-Section, but the Dr said that is a serious surgery & they only do it if something is wrong with the baby or mother...which #HELLO there WAS!! "But since you're fine and he's gone..we can't go that route!" Sooo...They started the pitocin drip @ 3:30 pm. & started contracting @ 6:50 pm. I only pushed for 16 min's & he came out @ 2:32 am. AS A "STILL BORN"..which is NUTS & drives me crazy because I felt him kickin me just the day before!!I signd off on a 3-way autopsy and it came back saying UNREMARKABLE.....UNREMARKABLE..UNREMARKABLE..on every square inch of him...UNREMARKABLE! A Picture Perfect #EarthAngel ..The only thing you will notice in some of the colored pictures is his skin peeling off. Kinda like when you take a long bath and your skin gets wrinkly...So when they wiped him down to clean him off some of his skin shed AND you'll see on his cheek it's in the shape of a HEART!! :( I thank you 4 all your prayer's NOW & 4 EVER!! *****Honestly I just feel honored & BLESSED that I was even able to carry him for nine month's and 2 know what it's like to be pregnant! I can't imagine the pain a woman must go through that cannot conceive at all. What a miracle birthing a child is..Angel or not! I AM WOMAN HEAR ME RAWRrrrrrrrrrrrrr!***** (((I Love You For 4EVER & EVER My Boy))) UPDATE: *Cayden is my one and only child *The baby and toddler in the video is my niece and nephew. *I still don't know what happened! (Stillborn is what the Dr's labeled this case as) *Everyone you see in the video is family or midwives/nurses. *Cayden's dad is not in this video. (The man I'm leaning on is my brother.) *Cayden would have been ten yr's old this July 10th 2018 and I still don't know why. I don't think I ever will know why...while I'm here on earth anyway, but I do believe one day I'll find out. That's for sure. And no doubt I got the best angel a girl can have!
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.
2 мес. назад
SUBSCRIBE to Barcroft TV: http://bit.ly/Oc61Hj An 11-year-old ‘diva' has become an Internet superstar and built up a vast following on social media - despite suffering from a super-rare ageing condition. Adalia Rose, from Austin, Texas, has racked up nearly 170 million views on YouTube and more than 13 million likes on Facebook with her hilarious videos showcasing her infectious personality. But Adalia has Hutchinson–Gilford progeria syndrome - a genetic condition characterised by the signs of accelerated ageing, which affects less than 500 people worldwide. In additional to premature ageing, other symptoms include dwarfism, lack of body fat and muscle, loss of hair, visible veins, a high pitched voice and stiffness in joints. For Adalia’s YouTube channel, check out: https://www.youtube.com/TeamAdaliaRose Video Credits: Videographer / director: Adam Gray Producer: Tom Midlane, Ruby Coote Editor: Sonia Estal Barcroft TV: https://www.youtube.com/user/barcroftmedia/featured Barcroft Animals: https://www.youtube.com/barcroftanimals/featured Barcroft Cars: https://www.youtube.com/user/BarcroftCars/featured For more of the amazing side of life: For the full story, visit BARCROFT.TV: http://www.barcroft.tv/ Like @BarcroftTV on Facebook: https://www.facebook.com/BarcroftTV Follow @Barcroft_TV on Twitter: https://www.Twitter.com/Barcroft_TV Check out more videos: https://www.youtube.com/user/barcroftmedia/videos Download Barcroft TV on iOS: https://itunes.apple.com/us/app/barcroft-tv/id1287734327?mt=8 Download Barcroft TV on Android: https://play.google.com/store/apps/details?id=com.recipe.barcroft&hl=en
7 мес. назад
http://beginnersmakemask.blog.fc2.com/ http://kumiko1.web.fc2.com/index.html I like making masks and this is Kyoko, my original character, I made with silicone, Platsil Gel-10. This is a tubby middle-aged man, changing into female. Am I looking a female?
4 г. назад
Before and after pictures of cinema star's teeth! See what improvements their teeth brought to them. Subscribe and like.
4 мес. назад
Please do not forget to visit the site http://scribol.com ************************************************************** Sometimes the most extraordinary events occur in the humblest of circumstances. Born in 1933, Lina Medina was brought up in the Peruvian village of Ticrapo. The town, perched at an altitude of more than 7,000 feet above sea level, was one of Peru’s poorest neighborhoods. Little is known of Lina’s very early years, but it’s easy to imagine that life in such a rural and impoverished area would have been basic. Apparently, she had eight siblings, and they were all raised by their mother, Victoria Losea, and father, Tiburelo Medina, who was a silversmith. Day-to-day life for the South American family would have probably been pretty uneventful. However, when Lina was five, something happened that would change her life – and her family’s – forever. Not only that, but it would shock the entire world. Concern for Lina started when the little girl began developing a bloated abdomen. Moreover, the swelling didn’t go down; on the contrary, it seemed to get bigger and bigger. Naturally very worried, Lina’s mother and father suspected that their daughter could be suffering from a tumor. But before heading to the hospital, they sought help from a curious source. The family reportedly asked local shamans to see if they could cure Lina of her problem, and the shamans apparently believed that her strange growth could be down to her being possessed. So Lina’s father, Tiburelo, granted permission for them to exorcise his daughter in a bid to remove “the snake under her belly.” Whether or not this “exorcism” actually took place is unknown. If it did, it clearly didn’t work – but what happened next is known to have occurred. With Lina’s ever-growing bump still present, it was time to see some professionals. According to a 1939 article in TIME magazine, one of the shamans was with the Medina family when they finally took the girl to hospital in Pisco, Peru. And apparently, the female shaman begged a Dr. Geraldo Lozada, one of the hospital’s surgeons, to “exorcise” the “possessed” girl himself. Clearly, though, a medical professional like Dr. Lozada was not going to do such a thing. Instead, he did what any regular doctor would do and gave the girl an examination. Yet what he discovered would surely have come as a complete shock. ************************************************************** ►You can support the channel: PATREON https://goo.gl/KtaKrp ►Image credits: Image: via Rare Historical Photos Image: YouTube/Jhordan Muñoz ►web: http://watchjojo.com ► SUBSCRIBE US: https://goo.gl/Z4nZcg ► Follow Us On Google Plus: https://goo.gl/JYf9Rr ► Like us Our Facebook Page: https://goo.gl/C5Rv92 ► Follow On Twitter: https://goo.gl/PZ2U1R ►For more articles visit: http://scribol.com ►Article link: https://goo.gl/Ak6YvP #watchjojo
11 г. назад
Child Foundation supports children worldwide born with birth defects. Meet Baby Miracletina from Samoa. She was born September 1, 2007 and not expected to live for more than a few hours. Her parents would not allow her to slip away and were able to sneak milk to her and she became strong enough to go home to her loving family and Samoan community. Since arriving in the US, Miracletina has defied odds that were against her from the beginning and is now facing her first round of multiple life changing surgeries. Miami Children's top surgeons will donate their services, but it is up to Miracle's supporters to raise the hundreds of thousands of dollars needed to provide her with the necessary hospital expenses involved in such delicate and life saving surgeries. Please visit our website for more information and how YOU can support this precious "Miracle" that we are honored to provide assistance to. www.childfoundation.com You can make a difference and show this loving child that she deserves the quality of life that ALL children deserve. http://childfoundation.com
1 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