Radio Station Of Giant Humans Of The Past

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    5 Extraordinary People That Actually Existed In The Past

    5 Extraordinary People That Actually Existed In The Past

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    5 Most Incredible Sideshow Freaks 2

    The most bizarre and talented people you've ever seen, Part 2! A four-legged woman, a three-eyed man, a fart-o-maniac and more! Subscribe to Dark5 ► And don't forget to check out part one: Follow Dark5 on Google+ ► Like Dark5 on Facebook ► Warning, text spoilers below... Presenting the weirdest, strangest, most incredible sideshow freaks to ever grace the stage and be caught on tape (part 2) including the "invincible" sword-swallower Mirin Dajo, Zip and Pip, the dwarf pinhead sisters, Le Petomane the professional fart impersonator, Bill Durks, the famous three-eyed man with his alligator-skin wife, and Myrtle Corbin, the original four-legged woman. Music: "Into The Heat" by Dhruva Aliman Intro: "The Machine Thinks" by Kevin MacLeod (incompetech.com) Licensed under Creative Commons: By Attribution 3.0

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    REAL HYBRID ALIEN CREATURES CAUGHT ON TAPE

    Presenting some of the best pieces of alien footage that’ll make you ask the ancient question: Do aliens exist? These are the best and eeriest alien videos from the internet. Could some be real? WEBSITE FACEBOOK Music Private Reflection by Kevin MacLeod (incompetech.com) Licensed under Creative Commons: By Attribution 3.0 Gathering Darkness by Kevin MacLeod (incompetech.com) Licensed under Creative Commons: By Attribution 3.0 Aliens, strange unknown creatures and eerie apparitions. Could they be real? (Watch more

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    Top 5 Most Shocking Pregnancy

    Counting down the top 5 most shocking pregnancies from the unsettling to the downright bizarre. 13 Year Old Father - Mother Forces Daughter To Get Pregnant - Pregnant Boys - Baby Born From Dead Mother - Woman Pregnant For 46 Years - ----------------------------------------­­­­­­­­­­­­­------------ CHECK OUT THE DAILY VLOG CHANNEL- P.O BOX # 14015 2408 Lakeshore Blvd W. Etobicoke, On M8V4A2 Connect With Me: Twitter- Facebook- Instagram- Order a LandonProduction T-Shirt- VIDEO EDITED BY: Sasha Wood:

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    5 People with Body Oddities

    5 People with Body Oddities. This video on people with body oddities is similar to 2 video's we have done before. This video looks at 5 special people with body oddities and it was inspired by some of the suggestions we got. Again: be respectful please. Find us on... -- -- -- --

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    10 PEOPLE You WONT BELIEVE Actually Exist Compilation

    10 Unbelievable people that are real. Men and Women survived the impossible or born extraordinary with no vagina, 2 penises or 2 vaginas. We are also Here: Twitter: Pinterest:

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    The Tiniest Girl In The World

    Two-year-old Charlotte weighs less than eight pounds and wears the clothes of a newborn baby. At 22 inches tall, she is half the height she should be and her sisters can dress her up in their dolls' clothes. While it is clear that Charlotte suffers from primordial dwarfism, the type of her condition is not yet known. MOPD Type 1 is a serious affliction marked by repeated strokes and seizures, and sufferers rarely live past their third birthdays. MOPD Type 2 patients often live to be 30, and great strides are being made in treating the condition. Discover how the world's leading authorities on the disorder are striving to help Charlotte cope with her extraordinary life. . JOIN QUIZGROUP PARTNER PROGRAM: .

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    Chinas Sexual Revolution Documentary 720p Channel 5 Extraordinary People Discovery & Documentary

    Revolution and its sizzling Economic Revolution. But you haven't heard about its other great social upheaval - the Chinese Sexual Revolution - and like everything in that country it's happening at warp speed. It's China's version of the 60s revolution - on steroids. China's Sexual Revolution is the world's first glimpse - often using secret cameras - into this forbidden new China. It's a surprising portrait of the Chinese today: the new free love generation that's left their parents in shock; the booming sex industry that's creating an HIV crisis; the new generation of career women and feminists that suddenly wants it all - while millions of men feel left out. This long untold story goes back to the days of Chairman Mao, who made sexuality a great taboo. He ordered everyone to wear unisexual Mao suits, and forbid women from wearing sexy clothing, getting stylish haircuts, or even wearing make-up. Men and women were expected to be comrades - not lovers - though Mao himself enjoyed an emperor's sex life, seeking virgins to retain his "youthö". China's sexual libido was bottled up for 50 years, but now itÆs bursting loose, with dramatic effects on marriage, personal freedom and the government itself.

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    Is he truely having supernatural powers Watch Completely Before Commenting

    Please watch the complete video before posting your comments India is a country with people who make a small swamiji in to gods,they are not truly gods , they are perfect magicians , with perfect timing Video is from 2006 this video is not about Religions or any creed, Its just a way to show how superstitious beliefs are still Present in today's rural India, The people who you see in the video are just educating local villagers about How GOD People play tricks in disguise as a Saint I hope you all are Educated Share the video if you really like it . powered by

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    COBRA GYPSIES - full documentary

    An adventure with the indian gypsies, the new movie of Raphael Treza - Follow me: - Support me: Paypal donation: - French version here: - Listen to the soundtrack: www.soundcloud.com/treza/sets/cobra-gypsies-soundtrack - watch my first movie "Hallucinogen Honey Hunters ": - and "Night" Ghat", the prequel of Cobra Gypsies:

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    The Little Mermaid

    Little Shiloh Pepin has sirenomelia or "mermaid syndrome", a rare birth condition where her legs have been fused together at birth. In most cases, persons born with sirenomelia die at birth, or get surgery to separate the fused legs. Shiloh has defeated the odds in making it to her eighth birthday. Sirenomelia, alternatively known as Mermaid Syndrome, is a very rare congenital deformity in which the legs are fused together, giving them the appearance of a mermaid's tail. This condition is found in approximately one out of every 100,000 live births (about as rare as conjoined twins) and is usually fatal within a day or two of birth because of complications associated with abnormal kidney and urinary bladder development and function. More than half the cases of sirenomelia result in stillbirth and this condition is 100 times more likely to occur in identical twins than in single births or fraternal twins. It results from a failure of normal vascular supply from the lower aorta in utero.

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    Jeune Thaïlandaise La Plus Poilue Du Monde By .FM.

    L'hypertrichose est une maladie congénitale très peu répandue dans le monde, touchant une vingtaine de personnes seulement. Sous la forme de dérèglement hormonal, cette maladie se manifeste par une pilosité envahissante sur une partie du corps ou la totalité, comme c'est le cas pour la jeune Supatra Sasuphan. Âgée de 12 ans, cette petite thaïlandaise est entrée dans le livre Guinness des records, ce qu'elle explique avec une certaine fierté : « Je suis très heureuse d'être dans le livre Guinness des records. Certaines personnes travaillent très difficilement pour y parvenir, alors que j'ai seulement répondu à quelques questions ». Malgré son handicap, Supatra est l'une des meilleures de sa classe et souhaite devenir médecin : « Quand je serai grande, je veux devenir médecin, pour aider et soigner les gens ». Certains spécialistes pensent que la légende des loup-garous vient des personnes atteintes d'hypertrichose, leur visage étant souvent entièrement recouvert de poils .FM.

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    11 Men You Wont Believe Actually Exist!

    Men you won’t believe exist! These unbelievable photos will make you question your belief in what's actually real vs fake. World's most hard to believe people ever! This is Tom Staniford who has been diagnosed with an extremely rare condition called MDP syndrome (only affecting 8 people in the world). His condition causes him to be unable to store fat underneath his skin. In contrast to what you might think, he has high levels of fat in his blood which caused him to develop Type II diabetes. Tom is an avid Cyclist and is a British National Paracycling champion. At 453 body piercing, Rolf Buccholz has the world record for the most number of piercings. Before you say you’ve seen people with more piercings, you should know that 278 of them are in his genitals. Interestingly the only other rolf I know is the dog from the muppets. Mr boo choltz did not start piercing until he was age 41. He says his palm tattoos were some of the most painful. He was actually denied entry into Dubai because based on his appearance he was suspected of black magic. This is Jeremey meeks aka Hot Felon. This guy is almost as hot as me. Jeremy Meeks was arrested on Felony weapons charges and when the police posted his mug shot he became an internet sensation. He will be sentenced on January 22, 2015 Patrick Deuel was once one of the heaviest men in the world. Weighing 1072 lbs (486kg) he was know as the half ton man. After a gastric bypass surgery he lost 570lbs (260 kg). What I never understand about these cases is how the people are getting food. Who is the person that is providing them with like 20 big macs? It turns out he is married and his wife did the shopping. This is Arlindo de Souza who injected his arms with synthol. Synthol, or site enhancing oil, is a mixture of oil and alcohol that can be injected into muscles to give them a greatly inflated appearance. Sort of like stuffing a sock down your shorts. Synthol does not translate into any increased strength. Also unlike real muscle, synthol muscles can droop excessively. While we’re on the subject of muscles here's another image. Now some websites suggest that this is another case of synthol and/or anabolic steroids but I don’t buy it this image looks photoshopped to me. Furthermore many suspect that Moustafa Ismail, who holds the Guiness book of world records for the biggest arms may have used synthol. Do you think he has? This is Amoo Hadij an 80-year old Iranian man who claims he hasn’t bathed in 60 years. He fears that cleaning himself will make him sick. To be honest besides the dirt he looks pretty good for 80, maybe he’s been in like a 60 year mud bath. In addition he says he smokes animal poop… clearly Amoo doesn’t give a shit...he smokes it. You maybe looking at this photo and thinking well that’s a tiny cell phone. Nope it’s actually a normal sized cell phone and this guy just has a really big hands. This was (Leonid Stadnyk) who was reported to be the tallest main at 8’5” or 2.57M making him taller than Bao Xishun of china who stands at 7’ft 9 (2.36M). however he refused to be measured by the Guiness book of world records. By the way The tallest man to ever live was Robert Wadlow who was officially recorded at 8ft 11in (2.72M) On the opposite end of the spectrum we have Chandra Bahadur Dangi (dangee). who is the shortest man to ever life. He is 1ft 9 ½ inches or 54.6 cm tall and is currently 75 years old. His condition is called Primordial dwarfism. This is Yu Zhenhuan (jen juan) who is listed as the hairyest man in the world. He does looks quite hairy although I seem to remember some mexican children who had hairer faces. As you might imagine dating is difficult. He did have a girlfriend for over two years but apparently her family objected to them getting married. This is Paul Karason aka papa smurf. The reason his skin was blue is that consumed an excessive amount of colloidal silver in order to treat dermatitis on his face. He admitted that the silver didn’t actually solve his dermatitis condition. But he said it helped with his acid reflux and arthritis. The bluish tint of his skin is a condition called Argyria (r-geeria). He died at age 62 of a heart attack but his death is not believed to be related to his silver consumption. Apparently Silver has antibacterial properties and before the introduction of Penicillin used to be used to fight infections. Kaleem is not a man yet but his pictures are some of the most unbelievable. At 8 years old, His hands have grown enormously measuring 13 inches from palm to his middle finger tip. He has difficulty dressing and feeding himself. As you might imagine he has had to deal with bullying in schools and he does not attend school because the teachers have told his family that the other children are scared of his hands. Unfortunately because his family earns only $23 month, it is difficult for him to even get a diagnosis.

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    The 46 Year Pregnancy - Extraordinary People Documentary

    The 46 Year Pregnancy - Extraordinary People Documentary This episode is about Zahra, a 75 year old woman from Morroco, admitted to the hospital for abdominal pains. To the surprise of the doctor, the pain was due to a baby, mummified in her womb from a pregnancy 46 years earlier. The second part of this episode is about Jane Ingram...who gave birth to a baby that developed outside of the womb, in her abdomen.

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    10 HUMANS WITH REAL SUPER POWERS IN THE WORLD

    WORLD'S 10 HUMAN WITH REAL SUPER POWERS, These are 10 extraordinary people/ human with super power or in short super human!!! Enjoy THANKS FOR WATCHING PLEASE SUBSCRIBE TO MY CHANNEL FOR MORE TOP 10S "SHARE & LIKE IT" music:Music4YourVids.co.uk SUPER POWERS list: michael lotito,can eat anything, kim peek :remembers everything, thai ngoc: the insomniac;staying awake forever, wim hof:withstand extreme cold, ma xian:electric man, masutatsu oyama:god hand natasha demkina:xray girl, isao machi :samurai man, liew thou, magnetic man PHOTO ATTRIBUTION wim hof Aad Villerius (www.flickr.com/photos/daaynos )1 kim peek Dmadeo1 isao machii 2008kgu 1 natasha 1 scott flanzburg Attribution: Scott Flansburg 1 humans with supernatural abilities!! Do human have supernatural powers? is it possible for humans to have supernatural powers? check this out thanks

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    The Woman Who Dives The Deepest - Extraordinary People - Documentary

    New Video: Most people can hold their breath for forty seconds, Tanya Streeter can hold her breath for over six minutes. Diving to the ocean floor on a single breath is an ancient skill among pearl and sponge fishermen, but only in the last 20 years has it become an internationally competitive sport. It requires superhuman levels of stamina and fitness.

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    40 Year Old Child: A New Case . - the little girl who doesnt grow.

    40 Year Old Child: A New Case - TLC revisits the Williams family in Billings, Montana, whose 8-year-old daughter Gabby suffers a mystery medical condition that slows her rate of aging. The Williams along with a handful of other families are facing the unknown when battling against this bizarre and inexplicable syndrome that affects the growth and overall development of their children, from blindness and deafness to the inability to walk, eat or even speak on their own. Following the everyday lives of these families and the doctors who have dedicated their careers to studying the signs of aging and are determined to find an answer. 40 Year Old Child: A New Case Air date: Aug 19, 2013 | TLC Specials Genre: Documentary, Family

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    The Tiniest Boy In Britain - Extraordinary People - Documentary

    New Video: The story of two-year-old Alex Connerty, Britain's only primordial dwarf. Alex was born with an extremely rare condition that has stunted his development and means that he will grow to be no taller than three feet. This film follows Alex and his family as they travel to the US to meet the world's only expert in primordial dwarves, in the hope that he can tell them what their son's future holds.

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    Hope For Hayley

    Progeria sufferer Hayley Okines and her family search for a cure for her debilitating disease. Hayley's story was catapulted into the limelight after she starred in documentaries called The Girl who is Older than Her Mother and World's Oldest Teenager. Her family is hoping a breakthrough in science might help her live a long and better life than previous sufferers who have died of the disease. Hayley said: 'I feel like I have a future to plan. I think that maybe when I grow up, I will get married. Mum says it will have to be someone very special to see beyond my progeria.' Last year Hayley's mum told it was hard letting go of the reins as Hayley grows up: 'It is difficult. She obviously wants to go out and I do let her go down to the local shops and go on sleepovers. She also goes to the local shopping centre with her friends but I like to be somewhere in the centre at the same time and I make sure she has her mobile on her in case she needs me.' The internet has opened up a whole new world for Hayley, who loves the social-networking site Twitter. It was thanks to her Twitter followers that she achieved a lifelong dream of meeting the pop singer Justin Bieber. Hayley's younger brother Louis and sister Ruby consider her to be a 'celebrity' because she's been on Blue Peter and met famous people. But she is increasingly aware that she has a terminal illness and has been shown laying flowers for a family friend with progeria who died at 14.

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    Top 5 People you Wouldnt Believe Exist

    Top 5 People you wouldn't believe exist. The dirtiest man, the women with the widest hips, turtle boy. These people are all very unique and special to say the least. 5. Dirtiest Man Alive The 80 year old Amoo Hadji is known as the dirtiest man alive. He has not bathed or showered in 60 years. He looks like a troll or maybe a creature from The Lord of the Rings. His skin is scaly, you can barely see his eyes and he smells to high heaven. He doesn’t have a skin disease or a terrible condition. For unknown reasons, he has simply refused to take a bath for the last sixty years. 4. Turtle Boy Didier Montalvo was born with a rare birthmark: congenital melanocytic nevus. Which means that his mole grew so big that by the age of six it covered his entire back like a turtle’s shell, earning him the nickname of Turtle Boy. 3. Sain Mumtaz Sain Mumtaz is known to have the biggest head in the world. When he was a boy he was told it was Proteus Syndrome and nothing could be done to help him. However, it is still not sure that Proteus is the correct diagnosis for his condition, but if it is there is nothing that can be done to reduce the weight of his massive head. 2. Most Pierced Woman Elaine Davidson is the most pierced woman in the world. She holds the world record for most piercings, over 9,000 and counting! An interesting fact: she has 500 piercings in her genitalia alone - both externally and internally. 1. Worlds Widest Hips Mikel Ruffinelli currently holds the record of having the widest hips in the world. Her weight is more than 420 pounds (190 kg) and her hips measure an unusual 8 feet (2.4 m) in circumference, even though her waist is only 3 feet 4 inches (102 cm). Find us on... -- -- -- --

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    15 People with Extra Limbs & Body Parts

    From third nipples on celebrities to unborn siblings growing limbs all over your chest and back, we count 15 of the most bizarre appendages ever to sprout on the human body. Facebook: Twitter: Gaming Channel: For my gaming livestream where I typically play retro console games like NES, Gameboy, Atari, PSX, etc, visit (and click FOLLOW to be notified for when I go live) Click here for the written version of this video: Come work for PLANET DOLAN! You can find job listings here: Legal notes ---------- Background audio copyright Kevin MacLeod (incompetech.com) Licensed under Creative Commons: By Attribution 3.0

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    10 Year Olds - Terri Calvesbert: Extraordinary People - Documentary - My Shocking Story

    New Video: Terri Calvesbert suffered 85% burns as a 2 year old. This film explores Terri's past, present and future, now she is aged 10.

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    Top 10 Amazing Places On Earth You Wont Believe Are Real

    The world is home to some truly surreal places that we must experience first-hand to believe its authenticity. We take a look at the top 10 amazing places on earth you won't believe are real! Subscribe! (new video every 2 days) -

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    The Worlds Oldest Conjoined Twins

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    The Woman With Half A Body - Extraordinary People - Documentary

    New Video: Rosemarie Rose Siggins Born with a rare genetic disorder known as Sacral Agenesis, Rose had severely deformed legs with feet pointing in opposite directions. There was no feeling in the legs and, as a child, she was in danger of harming herself. When she was two years old her mother, after consulting with the doctors at the hospital, decided that the best course of action was to have the legs amputated. This insightful decision by her mother allowed Rose to lead a fairly normal childhood. Rose grew up, with her mentally handicapped brother, in Pueblo, Colorado. Rose believes her parents made the right choice as she cannot imagine being confined to a wheelchair. She describes her physical condition in her own way "If you take a Barbie doll and remove it's legs, the region you are left with is what I have. I have all the female working organs, the only reason I sit shorter or more compact, as people say, is because I'm missing four sections of my spinal column". Rose's great passion in life is cars. All things automotive, cars, trucks and V-8 engines have been a big part of her life since she started playing with her father's toolbox at the age of 3. When she was sixteen, her parents bought her a car. A used car which Rose and her father adapted with hand controls so that Rose was able to drive herself around. She is rebuilding a 1968 Mustang which she plans to race. For years, the administrators at the local school forced Rose to wear artificial legs, they wanted her to look like everybody else. When she was in eighth grade she rebelled and refused to wear her prosthetic limbs, turning up for school on her skateboard. She wanted to be normal, and her normal is Rose who walks on her hands and has no legs. After meeting with her parents who were being very supportive, and realising that Rose was very stubborn, the school relented and allowed her to return, without her prosthetics. In 1997 Rose met Dave Siggins who worked in an auto-parts store, they flirted over the phone and their relationship quickly blossomed, but it was going to put Rose's life in danger. When they decided to get married, Dave joked with her that she didn't have to worry about getting cold feet. Rose and Dave were married in 1999, it was her dream come true. It was a traditional white wedding and Dave, still joking, pointed out that the cake was bigger than she was. Rose and Dave lead a normal sex life, the only comment Dave has made are that the legs don't get in the way.

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    The Boy Who Lived Before - Extraordinary People - Documentary

    New Video: Ever since he was two years old and first started talking, Cameron Macauley has told of his life on the island of Barra. Cameron lives with his mum, Norma, in Glasgow. They have never been to Barra. He tells of a white house, overlooking the sea and the beach, where he would play with his brothers and sisters. He tells of the airplanes that used to land on the beach. He talks about his dog, a black and white dog. Barra lies off the western coast of Scotland, 220 miles from Glasgow. It can only be reached by a lengthy sea journey or an hour long flight. It is a, distant, outpost of the British Isles and is home to just over a thousand people. Cameron is now five, and his story has never wavered. He talks incessantly about his Barra family, his Barra mum and Barra dad. His Barra dad he explains was called Shane Robertson and he died when he was knocked down by a car. He has become so preoccupied with Barra and is missing his Barra mum so badly that he is now suffering from genuine distress. Norma considers herself to be open-minded, and would like to find out if there is any rational explanation for Cameron's memories and beliefs that he was previously a member of another family on Barra. Her first port of call is Dr. Chris French, a psychologist who edits The Skeptic magazine which debunks paranormal phenomena. Not surprisingly, he discounts any talk of reincarnation mooting that a child's over-active imagination can be fed by the multitude of television programmes available and the easy access to the Web. Norma is not convinced, she does not believe that Cameron has ever watched programmes that could have provided this information. Norma's next step is a visit to Karen Majors, an educational psychologist whose speciality is children and their fantasy lives. She considers that Cameron's accounts are very different to normal childhood imaginary friends. It has become clear to Norma that there are no easy answers to the questions thrown up by Cameron's memories. Cameron has asked, persistently, to be taken to Barra. Norma has finally decided to make that journey.

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    The Girl Whos Older Than Her Mother - Extraordinary People - Documentary

    New Video: This is a story about Hayley Okines who has progeria, a very rare disease that causes rapid aging in children. Hayley Okines is an English girl with the rare aging disease progeria who is known for spreading awareness of the condition. Although the average life expectancy for sufferers is 13 years, Hayley is part of a drug trial that has seen her beat the doctors' predictions, and she is still alive and well. Diagnosed in 1999, being 2 years old, Okines was born with progeria, a genetic disease that causes her to age eight times faster than the average person. This puts her projected lifespan to age thirteen. She frequently travels from England to Boston to receive new treatments in the United States. Progeria (Hutchinson Gilford Progeria Syndrome) is an extremely rare genetic disease wherein symptoms resembling aspects of aging are manifested at a very early age. The disorder has a very low incident rate, occurring in an estimated 1 per 8 million live births. Those born with progeria typically live to their mid teens and early twenties. It is a genetic condition that occurs as a new mutation, and is rarely inherited. Scientists are particularly interested in progeria because it might reveal clues about the normal process of aging.

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    The Twins Who Share A Body Extraordinary People

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    The Girl Who Never Ate - Extraordinary People - Documentary

    New Video: The story of Tia McCarthy, a seven-year-old girl with a rare disorder in which her oesophagus and stomach are unconnected. Despite corrective surgery, she has never eaten a morsel. Tia McCarthy is 7 years old and she has never eaten anything. She is fed through a tube into her stomach and she never gets hungry or thirsty. Her mother Sue is desperate for a solution to be found to this puzzling problem before it is too late. With medical opinion in Britain unable to find a solution, Sue is preparing to submit Tia as a research case to the one of the world's leading specialists in the art of encouraging children to eat. This film follows Sue and Tia as they head to Austria to meet Dr Marguerite Dunitz-Scheer, whose programme of 'controlled starvation' boasts a near perfect success rate. The film follows Sue's emotional journey as she hands her child over to the woman who she hopes can do the one thing no one else has ever managed - teach Tia to eat. UPDATE : A ten-year-old girl has delighted her family by eating food for the first time in her life. Tia-Mae has spent a decade being fed through a tube because she refused to consume anything in the usual way. Despite being seen by a host of experts and flown to a specialist clinic in Switzerland the youngster refused to eat. Recently her mum Sue McCarthy, 44, offered her some yoghurt and was amazed when she accepted. Now Tia-Mae has soup for lunch, followed by custard or ice cream and the same again for dinner. She also consumes Angel Delight, mousse, custard and semolina. At night she is still fed nutrients through a tube, but her mum hopes that in time she will be eating like all her friends. Born three months prematurely with a large gap between her oesophagus and her stomach, Tia-Mae spent most of her first year in hospital. But there was no medical reason why she couldn't eat food and the condition baffled everyone. Now the family from Alderholt, near Bournemouth, Dorset, finally believe they are close to their daughter being able to eat enough to stop having to give her the extra nutirents. Mum Sue said: "It's lovely to see her eating. "We can go out for dinner now. I take a little pot of soup for her and she sits and eats with us. Then for pudding she chooses ice cream or custard. "I can't believe that just before Christmas, all she was eating was a few mouthfuls of yoghurt and now we have got this long list of things that she will sit down and happily eat. "I never thought it would happen. "I keep thinking of her future, when she's out and about, meeting friends, going to the pictures - normal stuff that children do. "I don't want her to miss out on all that. I think it bothers me more than it bothers her. "The specialist has been my light at the end of the tunnel. "Because no-one knew what was wrong with Tia, they didn't know how to help us. I was left on my own, with no idea what to do. "We've now got little steps that are achievable and we feel much more positive about everything."

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    The Musical Genius

    Derek Paravicini is autistic, blind, retarded, and yet, is a genius at the piano. He can play anything he hears just once. This reports follows him to a major concert where he teams up with another genius pianist...with the same handicap. Born three and a half months prematurely, Derek Paravicini miraculously survived, but his twin sister did not. Technically, he died three times in the hospital and his eyesight was destroyed by an oxygen overdose. He has been left completely blind, partly autistic, can't tell left from right and cannot count to ten, but despite his disabilities he has an incredibly acute sense of hearing, and is a musical genius.

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    The Girl Who Never Ages - Extraordinary People - Documentary - A Child Frozen in Time

    Brooke Greenberg (January 8, 1993 -- October 24, 2013) was an American from Reisterstown, Maryland, who remained physically and cognitively similar to a toddler, despite her increasing age. She was about 30 inches (76 cm) tall, weighed about 16 pounds (7.3 kg), and had an estimated mental age of nine months to one year. Brooke's doctors termed her condition "Syndrome X". Unexplained Conditions Over several years, the Greenbergs visited many specialists, looking for an explanation for their daughter's strange condition, yet there was no diagnosis of any known genetic syndrome or chromosomal abnormality. In 2001, when Dateline documented Brooke, she was still the size of a six-month-old infant, weighing just 13 lb (5.9 kg) at 30 inches (76 cm) tall. The family still had no explanation. Brooke's mother Melanie said, "They [the specialists] just said she'll catch up. Then we went to the nutritionist, the endocrinologist. We tried the growth hormone...". The growth hormone treatment had no effect. Howard, Brooke's father, said: "I mean she did not put on an ounce or she did not grow an inch ... That's when I knew there was a problem." After the growth hormone administration failed, the doctors, unable to diagnose a known condition, named her condition Syndrome X. The Greenbergs made many visits to nearby Johns Hopkins Children's Center, and even took Brooke to New York's Mount Sinai Hospital, searching for information about their daughter's condition. When geneticists sequenced Greenberg's DNA, they found that the genes associated with the premature aging diseases were normal, unlike the mutated versions in patients with Werner syndrome and progeria. Help share knowledge by sharing this video Have you heard of Brainwave Power Music? Check it out here Subscribe to the Youtube History Channel Documentary Some other great channels to check out Extraordinary People RC World Have you heard of Brainwave Power Music? This new trend of sound therapy is growing in popularity, from relaxation music and meditation tones to Lucid dreaming and astral travel. People are learning to unlock the power of their minds with the power of Brainwave Power Music. Click below to check out the channel

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    Strangest Birth Defects

    World's weirdest birth defects. These 5 Very Bizarre & Rare Birth Defects are so strange that they are often mistakes for hybrid creatures or alien beings. - There’s a condition called Fibrodysplasia Ossificans Progressiva - With this disease people grow bone in injured areas where we would normally grow back skin or tissue. - As they progress in life so much excess bone forms it begins to fuse their joints & become very debilitating. - Surgery isn’t an option because if the excess bone was removed even more bone would form in its place as their body heeled from the surgery. - Anencephaly is where a baby is born without a spinal cord or brain, and they typically die during childbirth - Some survive born with a basic brain stem but they are usually blind, deaf & unable to feel pain. - And without cerebrum they never gain consciousness, But they do have bodily reflex reactions to sound or touch & can breathe. - Cyclopia, named after the famous mythical creature, Is exactly what you’d expect. - A child is born with just 1 eye in the middle of their head. - As far as we know there were no cases in ancient Greece that started the mythology. - Cyclopia seems to be a modern defect believed to be caused as a side effect by certain cancer treatment drugs taken by pregnant women. - Craniopagus Parasiticus Is a condition similar to siamesee twins but in this case there is only an extra head from an unborn twin attached to the normally developed child. - Of 10 recorded cases only 3 survived birth. - And in only 1 case was the second head functional., able to suckle, blink, cry & even smile - Foetus in Foetu is a condition where a persaon is born with his twin inside of them, usually making them look pregnant. - The twin inside basically lives off it’s sibling like a parasite in the body. - Fortunately here surgery CAN usually remove the undeveloped twin with no lasting effects on developed sibling. Video Creative Commons Attribution Vimeo: 1) Growing the Brain Veins [Particle Flow Frost Tutorial] © Particle Skull (Vimeo) Find us on... -- -- -- --

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    5 People With Extra Body Parts

    Introducing 5 incredible people with extra body parts. Visit our site: Like us on Facebook: Follow us on Twitter: Song: MK2 - Dark Lotus 5 People With Extra Body Parts

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    The Boy With The Incredible Brain - Extraordinary People - Documentary

    New Video: This is the breathtaking story of Daniel Tammet. A twenty-something with extraordinary mental abilities, Daniel is one of the world's few savants. He can do calculations to 100 decimal places in his head, and learn a language in a week. He also meets the world's most famous savant, the man who inspired Dustin Hoffman's character in the Oscar winning film 'Rain Man'. This documentary follows Daniel as he travels to America to meet the scientists who are convinced he may hold the key to unlocking similar abilities in everyone.

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    Extraordinary People - Danielle Griffin - the worlds smallest girl

    Extraordinary People - Danielle Griffin - the world's smallest girl danielle griffin, danielle griffin 2013, danielle griffin part 1, danielle griffin part 3, extraordinary people, extraordinary people daniel griffin, extraordinary people daniel, small girl

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    5 Most Amazing Surgeries on People

    5 Most Amazing Surgeries on People. These are some of the most amazing surgeries ever performed. Xiaolian's surgery was in the news only recently. Other surgeries in the list are even more amazing! La mejor sirugia Find us on... -- -- --

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    Dangerous Growths - Extraordinary People Documentary Tanya Angus

    Dangerous Growths - Extraordinary People Documentary About video: A woman who suffered from a rare condition which made her grow into a 6ft 11ins giant has died suddenly at the age of 34. Tanya Angus, from Las Vegas, spent the last 12 years trying to find a cure for her acromegaly, which meant she couldn't stop growing. Until the age of 21, Tanya was just 5ft 8ins tall and weighed 130lbs. She rode horses, went dancing and had a boyfriend. Rare disorder: Tanya Angus was a slender 5ft 8 and 130lbs as a teenager, pictured here in 1995 (left). By 2010 (right), she was 6ft 6in and more than 400lbs. She died suddenly today at the age of 38 An inspiration: Tanya Angus celebrates her 34th birthday with a friend on November 27, 2012 Struggle: Miss Angus has died at the age of 34 after her heart failed due to her extreme size But a tumour became wrapped around her pituitary gland, causing massive amounts of growth hormone to be released into her body. Tanya, who became wheelchair-bound, had the most extreme form of acromegaly ever seen, growing to nearly 7ft tall, and more than 400lbs. Ms Angus, who had been working as a supervisor at a Walmart in Michigan, was fired from her post when her condition worsened, and was dumped by her boyfriend when his parents questioned whether she was a man. But she never gave up searching for a treatment to halt her incredible growth and hoped she could one day have a more normal life. In August last year, it seemed like Tanya and her family had finally seen a breakthrough, when a blood test revealed that her growth hormone levels had fallen at last. Tanya's mother Karen Strutynski said at the time: 'For the first time ever, Tanya's blood level for her disease is in the normal range. 'It gives us renewed hope and will give other people renewed hope. New treatment: The 34-year-old was given renewed hope for her condition last year but it was not to last The good news was short-lived. Tanya's Insulin-like Growth Factor levels, which had fallen from 3,000 at the worst of her condition to just 283, had started to creep back up into the 500's. The normal range for a healthy person is around 250. It is thought the extreme pressure on her body, caused by 12 years of coping with her huge size, caused her heart to fail. A notice on Tanya's website, which has inspired and helped acromegaly sufferers around the world, reads simply: 'It is with deep sorrow that we announce the passing on of our beloved Tanya Angus at 12.25am on January 14, 2013, due to her heart and TIA. RIP dear one' Transient Ischemic Attack (TIA) is a type of mini-stroke, caused when the blood flow to the brain stops for a period of time. Tanya had suffered a number of TIAs in recent years. Describing her acromegaly last year, Tanya said: 'Sometimes I feel really down about it but to me the most important thing is that I have to tell people about it. 'I read emails that people send in saying: ''You're my inspiration,'' or, ''You are so strong.'' 'If I am helping other people, I feel I can do anything.' Tanya, whose condition caused her to spend many hours sleeping, found her outlet through her website, which helped her gain friends around the world. Last year, she was able to meet some of them for the first time at an Acromegaly Conference in Las Vegas, where fellow sufferers told Tanya how hearing her story had caused them to seek early treatment, and possibly saved their lives. During the last 12 years, Tanya underwent three operations to attempt to remove her tumour, but several different surgeons were unable to reach part of the growth, as it was wrapped around her inner carotid artery. Her heart, lungs and the joints of her limbs continued to grow as she gained weight and height, causing huge strain on her body. Healthier times: Before her acromegaly diagnosis, Ms Angus was a keen horserider Her mother Karen and stepfather Allan continued to search for new ways of tackling her condition, and last year doctors finally agreed to double the dose of Tanya's growth inhibitor medication, which was administered by painful injections into her spine. The treatment seemed to finally be working, until the sad news in October that her growth hormone levels were rising again. Tanya, talking in 2009 about the slow onset of her growth said: 'I couldn't understand why, as I wasn't eating more. What was strange was that my feet seemed to grow as well. My face also started to swell and was changing. 'I felt unhappy with my appearance and spent a fortune on make-up. My figure also started to change and become more manly and my voice became deeper.' tags: Dangerous Growths,Extraordinary People Documentary,Full Face Transplant,tanya angus acromegaly,Extraordinary Story,Faces of Death,Mystery Diagnosis,jacqueline saburido,How To Lose Weight Fast and Easy,How To Lose Weight Fast,extraordinary people

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    The Woman Who Kept Falling Down - Extraordinary People - Documentary

    NEW VINES COMPILATION: Subscribe for more awesome documentarys! Extraordinary People, BBC, etc. This documentary as well as the rest of these documentaries shown here relate to important times and figures in history, historic places and people, archaeology, science, conspiracy theories, and education. The Topics of these video documentaries are varied and cover ancient history, Rome, Greece, Egypt, science, technology, nature, planet earth, the solar system, the universe, World wars, battles, education, biographies, television, archaeology, Illuminati, Area 51, serial killers, paranormal, supernatural, cults, government cover-ups, the law and legal matters, news and current events, corruption, martial arts, space, aliens, ufos, conspiracy theories, Annunaki, Nibiru, Nephilim, satanic rituals, religion, strange phenomenon, origins of Mankind, monsters " Drugs"ganglands,gangland chicago,gangs,what are gangs,blood gangs,chicago gangs,gang,la gangs,prison gangs,street gangs,white gangs,houston gangs,gangs in la,gangster,american gangsters,gangsters,rap,raps,rap songs,rap artists,American Gangster,Race War,Hate Nation,Blood Oath,Mongol Nation,Sin City,From Girl to Gangster,Latin Kings,Aryan Brotherhood,Gangsta Killers,Trinity of Blood,Capitol Killers,Valley of Death,Most Notorious documentary,hd documentary,documentary hd,full documentary,full documentary hd,documentary long,long,full,hd,the tribe that hides from man,the tribe that never was,the tribe that time forgot,tribe,south american tribes,tribes documentary,national geographic tribes documentary,native american tribes documentary,philippine tribes documentary,uncontacted tribes documentary,hunting tribes documentary,tribe documentary national geographic,tribe documentary part 1

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    Extraordinary People The Rainman Twins Full

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    Extraordinary People - The Girl Nobody Believed

    Young Kirsten Larson has always been a little heavier than most other girls, but at the age of eleven, she experiences dizziness and a burning sensation in her chest from even the slightest physical exertion. People believed she was suffering from simply being overweight, when actually, she suffers from primary pulmonary hypertension. Sean Keefer suddenly develops a sharp sensation in his eye, a fever, muscle aches, chronic diarrhea, and pain in his legs. Eventually, his muscles become so stiff that he can barely move at all. His doctor finds out that Sean has been suffering from Reiter's Syndrome the whole time.

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    The Mermaid Girl: The Last Six Months - Extraordinary People - Documentary

    New Video: Shiloh Pepin was born with Mermaid Syndrome, or Sirenomelia, one of the rarest conditions known to man. This condition means the foetus fails to develop normally below the waist, resulting in a fusion of the lower limbs. Of the few foetuses that actually make it to birth, most die within hours of leaving the womb. On October 24, 10-year-old Shiloh Pepin died after spending a week in the hospital with pneumonia. She stayed active and upbeat until the end.

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    Treeman The Cure Extraordinary People

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    The Twin Within The Twin - Extraordinary People - Documentary

    New Video: The twin within a twin is a reports on the phenomena of twin-to-twin transfusion syndrome, which occurs in developing twin fetuses, when one of the twins dies and is enveloped by the other or where both die because of unequal distribution of blood. New Video: This reports also looks at the case of Bengali farmer, Sanjay, who underwent an operation for what was believed to be a massive tumour in his stomach, but turned out to be the semi-formed fetal remains of his twin brother.

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    The Boy Who Sees Without Eyes - Extraordinary People - Documentary

    New Video: The story of Ben Underwood, a blind boy who has learned to develop skills which enable him to draw a detailed mental plan of his surroundings.

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    The Real Sleeping Beauty Extraordinary People

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    7 New Faces In 7 Days - My Shocking Story

    Vietnam has one of the highest incidences of birth defects in the world, which scientists have linked to the use of chemicals such as Agent Orange during the war. Children born today are still living with the legacy of the past, and, with expertise and facilities to help most of these patients sadly lacking, many families rely on the help of overseas charities and volunteer doctors. Facing the World is a United Kingdom-based charity that offers surgery to children with facial disfigurements. All the children offered surgery are from poor countries where they would have no other access to surgery to help them overcome their disfigurements. History: Facing the World was set up in 2003 by Norman Waterhouse and Martin Hirigoyen Kelly, two craniofacial plastic surgeons at the Chelsea and Westminster Hospital. Both had formerly volunteered their time and skills to medical outreach charities abroad, but had been touched by cases of children that they were unable to help because of the limited facilities and lack of expertise in the countries in which they were working. With Facing the World they determined to bring children to the UK for surgery, rather than attempting to perform the operations with the limited infrastructure of the children's home countries. Bringing the children to the UK allowed them to draw on the skills of other like-minded UK medical professionals. Sarah Driver-Jowitt was hired to manage the charity and in 2004 an office was established close to the London hospitals where the majority of the surgeries are performed. The charity was launched publicly on 15 February 2003 at a charity fund-raising premiere of the film Solaris attended by George Clooney and his co-stars. Operation: The charity provides treatment for children from poor countries who have severe facial disfigurements that have significant functional challenges or are likely to cause them deep emotional and psychological trauma as a result of community stigma. The children are assessed in their own country, so the doctors can ascertain whether the individual could be helped by surgery and what specialist care will be required. If the assessment is positive arrangements are made to fly the child to London for treatment. The medical team donate their services and the charity relies on fund raising and donations to fund the remaining medical costs, travel and accommodation for the child and a guardian.

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    The Baby With A New Face Extraordinary People

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    Extraordinary People: Help! Im 16 But Look 60

    When she was a young girl, Tracey was diagnosed with lipodystrophy, a condition that makes her look much older than she really is. It can also have potentially serious side effects, including diabetes and blocked arteries - increasing the risk of heart attacks, strokes and cirrhosis of the liver. Her daughter Zara inherited the same condition. Tracey, Zara and her 17-year-old sister Chloe (who does not have the condition) all travel to Texas. Zara wants cosmetic surgery advice from internationally acclaimed surgeon Dr Robert Ersek in Austin, and Tracey hopes to get a diagnosis from specialist Dr Abhimanyu Garg at the University of Texas Southwestern Medical Center in Dallas. Zara's dream of having cosmetic surgery comes true when Dr Ersek agrees to perform a facelift on his youngest ever patient. However, the news about their medical condition is far from clear-cut. Dr Garg informs them that they do not in fact have lipodystrophy, but an even rarer genetic condition called cutis laxa. This means that Tracey and Zara will not suffer the serious side effects of lipodystrophy, but cutis laxa is incurable and has serious medical implications of its own...

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    Human Mutations And Deformities TODAY

    Here are some of the most unusual genetic mutations and deformities TODAY

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    Killer Girls Documentary on Girls Turned Killers Extraordinary People New Documentary 2014

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    ▶ Maurice Tillet - NBC Sportsworld 1985 A Look at Professional Wrestling part 3 CUT YouTube 144p

    Maurice Tillet Speaks - Early 1940 at the Chicago Field Museum