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No One Wanted to Adopt Her Until Someone Found Out What Made Her So Unique



all of us are born unique and we continue to be unique throughout our lives but some babies are born more unique than others and shock their families when they’re born they then go on to shock the world from the most beautiful child in the world to the smallest child here are 20 most unusual kids in the world number 20. buyers in Hussein in 2016 the world learned about bayazid Hussein a four-year-old boy who looked more like an 80 year old retired man the young boy is from magura in the south of Bangladesh and suffers from a rare condition called Progeria this condition ages the human body eight times the average rate which means viazid as features more typically seen on people several times his age his face is swollen his eyes are Hollow his joints ache his skin sags he has bad teeth and he even has challenges passing urine it’s believed that viazid’s condition inspired the novel and movie The Curious Case of Benjamin Button sadly those with this condition often die from Strokes or heart attacks at age 13 on average which means they never live a full life according to his mother tripty katun her son is clever and it breaks her heart that he has an unusual appearance she said she was terrified when he was born and the doctors didn’t know how to help or treat him foreign to their village news of their child spread and people lined up to see him however they never supported him and children were too afraid to play with him by as it doesn’t attend school but does spend time with his cousins one like this video smash the Subscribe button and click the notification Bell right now or this centipede will crawl on your face when you’re sleeping now it’s time for the star topic adopting children is a significant decision for any family to make and this baby struggled to find a family willing to take her apparently she was born with a condition that meant she didn’t have any pupils was blind and had vibrant blue eyes according to her caretaker while she couldn’t see she had incredible hearing and could hear the tiniest sounds no one wanted to adopt her until someone found out what made her so unique it was once this skill was realized that adoptive families were lining up at the door do you think her unique abilities really helped her to be adopted comment down below with the hashtag startopic and let us know your opinion in relation to what we just showed on screen with that said let’s keep things moving number 19. shin hyomyung many people call Shin Hyun Myung the Peter Pan of Korea he has a condition called Highlander syndrome which stops his body from aging and even slows down his growth in 2015 when the world learned about shin he was 26 years old however he looked like a school student who hadn’t yet reached puberty he had a quiet voice chubby cheeks and was short however Shin is very much a grown adult and enjoys doing grown adult things like drinking alcohol going to nightclubs and dancing the night away because of his condition nightclub workers can sometimes mistake him for a child and only let him in once they see his ID and learn that he was born in 1989. Shin developed normally as a child but his growth stopped once he became a teenager despite his condition he’s still in good health and wants to do everything other people his age want to do such as meet a beautiful woman to call his girlfriend Shin also appeared in a documentary that attempted to give him a makeover and make him appear older to go on a date however he still looked young and his date was shocked when she learned how old he was number 18. Shiloh Pepin Shiloh Pepin was born with mermaid syndrome or siren Emilia which meant her legs were fused together and she had no genital organs or lower colon she also only had one partially working kidney doctors thought she would only survive days after her birth but she shocked them all by being what her mother described as a tough little thing and living for an entire decade while many children are able to have surgery to separate their legs Shiloh wasn’t a candidate her blood vessels featured from side to side of her circulatory system and they would have been severed doctors were able to give her the best chance of Life by performing two kidney transplants and the last one was in 2007. Shiloh’s story was shared with the world on the Oprah Winfrey show and other TV shows sadly Shiloh came down with a cult that turned into pneumonia her parents acted quickly by taking her to the Maine Medical Center for antibiotics and to be put on a ventilator and things were looking up for Shiloh however sadly her condition deteriorated and she passed away number 17. Christina pimenova every child is beautiful but how many children do you know who get called the most beautiful girl in the world just one and her name is Christina pimenova Christina is from Moscow Russia and in 2014 at eight years old she was named the most beautiful girl in the world Christina’s Beauty was realized from a young age and she was presented with many modeling opportunities at only three years old before long Christina was working for big names in the industry like Roberto Cavalli Fendi and Armani even at eight years old she had already appeared on the cover of Vogue Bambini and had a Facebook presence with more than 2 million likes as a child Christina strictly wore children’s clothes and rarely wore makeup hello much time has passed since Christina was called the most beautiful girl in the world she now lives in the United States and previously got involved in gymnastics she competed in a gymnastics tournament in the Republic of todderstand and won a gold medal in her age group she also appeared on the cover of Vogue kids in 2015 and in that same year moved to California with her mother Number 16. Richard sandrak children aren’t generally considered strong at least not next to adults but Richard sandrak was an exception to that rule Richard who was born in 1992 had an incredibly muscular physique from a young age and even appeared in a documentary called the world’s strongest boy Richard is a ukrainian-born American actor martial artist and former bodybuilder he was born in Ukraine to a martial arts world champion father and aerobatics competitor mother and moved to Pennsylvania with his family at age two not long after they arrived his training began his father introduced him to lightweight training and stretches using his knowledge of Taekwondo shortly after they moved to California to try and break into the show business here they met trainer Frank giardina and they hired him to help give their son some publicity by age six Richard can lift 180 pounds on a standard bench press which earned him the title of the world’s strongest boy by the time he was eight years old he was bench pressing 210 pounds and people were calling him Little Hercules I’m very proud of my past it’s not something that I don’t want Richard worked out with his father most days performing up to 600 push-ups and sit-ups and 300 squats with so much training he didn’t get to play with his friends or have a normal childhood he wasn’t even able to eat sweets or junk food due to the strict diet his father enforced so Richard’s childhood was Rocky to say the least and he quit bodybuilding in 2015 after becoming bored with it number 15. Ben Underwood Ben Underwood was an incredible young boy he was a blind American born in 1992 who sadly was diagnosed with retinal cancer at age two doctors had to remove his eyes to save his life when he was just three years old Ben could have let his lack of eyesight ruin his life but he didn’t he taught himself echolocation at just five years old and was able to detect the location of objects by making clicking noises with his tongue his story was told on the TV show 2020 medical Mysteries human echolocation describes a human’s ability to find objects in their environment by creating sounds to sense them some people tap their canes or stomp their feet While others might snap their fingers or use their mouths to make clicking noises Ben was a master at it and he used it to have a normal childhood doing things like riding a bike skateboarding playing basketball running and playing football he never let a lack of eyesight get in the way of doing what his friends did sadly Ben died in 2009 just one week shy of his 17th birthday the same cancer that took his eyesight returned and took his life number 14. John Chris kirante most people have a set of 20 baby teeth that start growing in from a young age as you get older they fall out and 32 adult teeth take their place but John Chris kirante from the Philippines is not like most people when we first learned about John Chris at nine years old he had 300 teeth he had already had 40 extracted and would need several more operations to remove the remaining excess ones eventually he would also need to wear corrective devices to fix his bite as unusual or unbelievable as it sounds to have 300 teeth it’s entirely possible John Chris has hyperdontia which describes having extra teeth that appear in addition to the standard number that he’s supposed to have they can grow anywhere in the dental Arch not just where teeth would grow but anywhere else often this condition goes hand in hand with another condition like Gartner syndrome or a cleft palate Gardener Syndrome causes non-cancerous tumors to grow while a cleft palate is a birth condition resulting in an opening or split of the lip and roof of the mouth John Chris never let his excess teeth affect him he goes to school where he excels and he has dreams of becoming a civil engineer number 13. Charlotte Garside Scott Garside and Emma Newman are just like any other parents in the respect that they want their children to have normal childhoods and even though their daughter Charlotte Garside was born with a rare form of primordial dwarfism they were determined to make sure she wasn’t an exception to the rule Charlotte’s condition is so rare that doctors haven’t even created a name for it at five years old she was just 26 inches tall and weighed 9 pounds basically she was around the size of a baby and her favorite teddy bear was bigger than her when she was born her doctors didn’t think she would live past age one and even though she has Health complications she was a happy five-year-old in 2012. her mother Emma said Charlotte was not the type of person who would Fade Into the background and had a massive personality she wanted to do everything like a normal five-year-old and was extremely inquisitive her learning age at age five was believed to be that of a three-year-old which was higher than they thought Charlotte has continued to surprise her family and exceed medical professionals expectations when she was warned she weighed less than two pounds measured just 9 9.8 inches and was dressed in doll’s clothing Emma used to carry her around in the front pocket of her hoodie and had a purchase credit card sized Diapers at age five Charlotte still wore clothes for newborn babies and was smaller than their family cat number 12. moon but jonav when zydullo bachonev saw his son for the first time he and his wife were stunned even as a newborn baby his eyelashes reached his lips that’s definitely not something you see every day doctors assured the couple that their baby was healthy but the gene responsible for eyelash growth wasn’t the same as most peoples now as a child moon is registered in the Russian book of records for having the country’s longest lashes something he’s okay with moon can’t walk down the street without people paying him attention for his long lashes but he’s not bothered by it Moon even says he lives like everyone else and doesn’t have to take special care of his eyelashes he said he’s comfortable with them and doesn’t have any difficulties in 2018 moon was 11 years old and his eyelashes were 1.7 inches long the average lash length is around 0.39 inches but Moon’s not alone with his long lashes you jingxia from China currently holds the world record his eyelashes were measured in Shanghai China at eight inches long number 11. Ava Clark when Ava Clark was just months old it became apparent to her parents that there was something different about her they were both brown-eyed African-Americans but Ava had blue green eyes bright pink lips fair skin and light blonde hair doctors diagnosed her with albinism which is a genetic disorder resulting in lack of skin eye and hair pigment it could affect anyone of any race and can sometimes result in Sun sensitivity and vision problems Ava has undergone several tests and exams since she was a baby and doctors were sure she’d be blind by age four [Music] she was even examined by the School for the Blind thinking she would need to go there although she surprised Everyone by attending a regular school and simply needing to wear glasses Ava is a beautiful young girl and her looks have put her in demand for modeling she has appeared in magazines like VIP Denim and boom and has also worked with celebrity photographers even casting directors have been seeing Ava’s potential but she’s otherwise an ordinary child and enjoys running ballet reading gymnastics and playing pretend sadly albinism can be life-threatening for many people especially those in Africa you see In some cultures the body parts of people with albinism are seen as magical so they’re kidnapped and killed grave robbers have even been known to dig up the corpses of people with albinism number 10. at least 10 Roberts in 2009 the world learned about a remarkable young girl called Elise tan Roberts at two years four months old she was called the cleverest child in Britain with an IQ nearly as high as Albert Einstein’s at 156. Einstein’s was 160. the average IQ is 100 and her IQ puts her in the top 0.2 percent range for children her age at just two years old she was also the youngest member of Mensa a high IQ Society for those who score in the 98th percentile or higher on an intelligence test elise’s parents knew there was something different about her at just a few months old she looked at her dad at just five months old and said Dada three months later she had mastered the art of walking and just two months later she was running before she even turned one she could recognize her written name and she could count to 10 by 16 months by two she was counting in Spanish when elise’s mother Luis saw a TV show about gifted children she decided to see if there was something extra special about Elise she called specialist educational psychologist Professor Joan Freeman to assessor and Professor Freeman said Elise was more than bright and capable she was gifted her parents aimed to keep her learning at an advanced pace and encouraged her not to dumb herself down to fit in by 2020 Elise was 14 years old and filming short educational films for schools she also worked as a news presenter for a children’s TV show called FYI number nine miliana Worthy some people think birthmarks are genetic While others say they’re random and the luck of the draw but it’ll be hard to debate genetics being involved when you see miliano worthy she has the same white patch of hair as her mother grandmother and great-grandmother miliana’s story came to light in 2016. the Ridgeland South Carolina baby was born with peliasis Lucid condition her family members have that results in a shortage of pigment in the skin and hair according to her mother Brianna she hoped miliana would have it but she wasn’t guaranteed to have it since her own sister born a few years after Brianna didn’t but she said as soon as miliana was placed on her chest she saw she had it and was so happy although she said it occasionally has its downsides they often get stopped in the streets when they are carrying out their daily routines while Brianna doesn’t mind most people asking questions she said it could be overwhelming at times especially when she’s in a rush she hopes her daughter will Embrace her unique hair as she gets older she also hopes that she won’t get called the same names that she used to such as Gunk she plans to raise her daughter to know she’s beautiful and special and not to listen to people who make mean comments number eight fiori yolana in 2018 five-year-old yaraelana from Nigeria was dubbed the most beautiful girl in the world after pictures of her went viral on social media photographer mofe bamoya shared official images of the young girl on Twitter and Instagram showing off her natural beauty she had piercing blue eyes a stunning complexion and Gorgeous Hair some people said she was a true work of art doll like and absolutely stunning most of the world agreed because the three photos uploaded to social media amassed almost 50 000 likes and thousands of comments according to mofa she took the images to portray the interception between childhood and adulthood the photographer also posed Yara as an adult so that the portraits would appear timeless it would seem that beauty runs in yara’s family but she’s not the only up-and-coming model her 7 and 10 year old sisters yomi and Yoba are also beautiful and have had their photos taken and shared online since then yari’s family has been in the spotlight Yara has appeared on the covers of multiple magazines and has even walked at pristine fashion shows number seven nariana in 2017 modeling agencies from around the world were tripping over themselves to meet and work with nariana noriana often called Siberian Snow White was an eight-year-old from yakusha Siberia with albinism she’s the only one in her family with blonde hair and the first family member on both sides with albinism according to photographer varim rufov she is the most unusual person he’s ever met he spent two hours with her taking photos even though her eyes don’t like bright light he managed to take some incredible pictures of her nariana’s family have received multiple offers from advertising and modeling agencies for her to work but given her young age they had turned them all down nariana’s family wanted to wait until nariana was old enough to make the choice for herself although it’s clear that nariana even at eight years old was more than willing to make the decision she said she wants to be a model when she grows up although for now she’s also just a normal kid who loves dancing and drawing number six Tessa Evans most of us are born with all necessary facial features like two eyes two ears a mouth and a nose but Tessa Evans from County Derry Northern Ireland wasn’t this young girl was born without a nose which is a condition called congenital orionia not only does she not have a nose but she also doesn’t have sinus cavities or a sense of smell according to Tessa’s parents grain and Nathan they struggled to come to terms with her condition when she was a baby Tessa had to be tube fed and had a tracheostomy tube in her neck they were also afraid of the unknown because they knew she would face some dangers in her life with no sense of smell she wouldn’t be able to smell smoke in a dangerous situation or rotten food to know if it were safe to eat or not however technology is incredible at two years old Tessa had a 3D printed nose implant fitted under her skin at four years old she also had a larger one inserted to keep up with her growth sadly an infection meant it had to be removed medical professionals intend to install a new nose implant every two years until she stops growing at 8 years old Tessa said having a new nose would make her really happy number five Kumar obesity is a growing problem throughout the developed world but you usually only see it become an issue from late childhood into adulthood in the case of chihat it started as a baby at just eight months old in 2019 Chad Kumar weighed 17 kilograms or 37 pounds which is the average weight for a four-year-old shahad had been born weighing a regular amount but she started growing at an alarming rate by the time she was four months old according to her father siraj her weight increases daily and both he and his wife Rina are worried about her health and the cause of her insatiable appetite they say she doesn’t eat like an average child and eats all the time if they don’t give her anything to eat she starts crying she also cries to get outside but her weight means they aren’t able to pick her up easily so they only take her to nearby places while some people blame them for chihat’s weight Suraj says it’s not their fault and that God gave her this condition he feels bad when people laugh at her for being fat even at a young age her weight was causing her issues she has breathing and sleeping problems and Dr says she has abnormally hard skin this is meant they aren’t able to take blood samples to learn about her condition the family also didn’t have much money but they did their best to ensure she got well number four Madden Humphreys Madden Humphreys was often bullied for having a cleft lip and palate and different colored eyes called heterochromia iridium the Oklahoman seven-year-old often felt alone especially as he didn’t look like all of his peers but that all changed when Valentine entered the picture Valentine was a cat born with the same two conditions as Madden and it looked like it was meant to be the cat was being offered up for adoption in Minnesota so the family traveled from Oklahoma to get the kitty that Madden renamed Moon according to Madden’s mother generous friends and strangers made the road trip possible so that they could adopt the cat for Madden she said she knew they were destined to be best friends and how it was funny that a pet could make you feel less alone mending Spirits animal rescue who had rescued the cat said they were thankful they could enable such heartwarming connections number three Robert Hogue Robert Hogue has led an incredible life and is the very epitome of the saying that beauty is subjective Robert was Mary’s fifth child and was born with a tumor in the middle of his face and mangled legs doctors think the antidepressants Mary took while pregnant might have caused the deformities Mary didn’t want to take her baby home and was worried that Robert would affect her other children she even wrote in her diary that she wished she would go away or die or something she wanted to be finished with it all and told the hospital staff she didn’t want her baby she even said that under no circumstances would she take it home and didn’t feel anything so she and her husband returned home without Robert before long Mary started second guessing her decision and gave her other children a say she made them vote on whether to bring their new brother home they all said she should so Robert finally joined the rest of the family Robert was relentlessly bullied throughout his life and had to undergo multiple surgeries but despite everything that he has endured he has had a wonderful life Robert was the first member of his family to go to college and became became a journalist and spokesperson for an Australian politician he also had the pleasure of carrying the Olympic torch has been married twice and has two daughters number two Juliana stro Iana Stroh wasn’t like any ordinary child the boy from Romania was entered into the Guinness World Records at just five years old for being able to perform the fastest 33-foot hand walk with this act he became a global sensation and went on to break the world record for the most 90 degree push-ups just one year later Juliana was the musliest strongest five-year-old you would have ever seen and he had some impressive Feats throughout his life he started copying his brother’s training routine when he was just 18 months old he and his older brother would lift heavy weights and dumbbells to build their chest and bicep muscles they also did boxing however most people didn’t hear much about him after he broke the Guinness World Record at age 17 he shared a photo of himself holding a photograph of him as a child he looked far different while wearing loose-fitting gym clothing number one supatra susafan supatra once won the title of the world’s hairiest girl she suffers from Amber’s syndrome also called werewolf syndrome that causes excess hair growth on her body and face she was named the hairiest girl in the world by the Guinness World Records in 2010 and at this point she had thick hair covering her face ears back arms and legs she tried many different treatment options including laser treatment but it failed to stop the hair growth but her hair didn’t stop her from living a normal life the 17 year old shaved her face and uploaded pictures of herself and her husband onto social media she looked happy and very much in love we’re all unique but it’s hard not to see these people as among the most unique of all of us sometimes they’re born with medical conditions and other times they’re unique in other ways were you born with a unique trait that other people don’t have feel free to share your story in the comments also check out our other cool stuff showing up on screen right now see you next time

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