believe it or not there's a boy in GUI Drautonomous region who has the ability to see clearly in the dark around 385,000 babies are born each day around the world each with its solitary identity yet there are people who make the world whisper behind their backs unique rare and exceptional let's meet these people who are only born once in a thousand years I was born with athor grap posis in the joints in my arms and legs they didn't develop all the way Ryan a 26-year-old born with arthrogryposis a condition causing joint Fusion in the arms and legs overcame his limitations and started to live independently as his joints are not fully developed he has creative ways to get done with his routine tasks as I got older I started figuring out how to do all these things although Ryan had problems growing up but as his life Journey began he mastered the ways to adapt to his surroundings Ryan is fond of using Tik Tok sharing his unique ideas and creativity with over 111,000 followers Ryan's philosophy centers on staying true to oneself amid life's challenges promoting self-acceptance in a world often marked by negativity Ryan has big plans of becoming the most successful human in the world and nothing in his way can stop it from happening only if he believes in himself Face Changer family the monang family born in Indonesia whose faces exhibit a unique genetic condition causing permanent alterations characterized by fragile skin and overgrown gums they face societal misconceptions and job discrimination due to their distinctive appearance the family refuses medical diagnosis leading to speculations about inbreeding and curses the Elder brother responsible for his siblings struggled with employment but found acceptance online gaining over 300,000 YouTube subscribers and 2 million Tik Tok followers this family highlights the importance of online Platforms in creating an accepting environment Joseph Williams Joseph born without a jaw due to a rare condition called autof facial Found Love and married Venia communicating through text to speech apps and in Sign Language the couples love blossomed he used the text to speech app and also to with sign language he taught me alphabet so I know from A to Z the alphabets leading to an immediate Courthouse marriage both families while initially skeptical now appreciate the unique qualities each brings to the relationship the couple challenges societal Norms emphasizing the importance of understanding and accepting differences in relationships vinia overcame social judgments and St stereotypes about their relationship their story underscores that love with its power and adaptability surpasses physical attributes offering valuable lessons on patience acceptance and embracing diversity claudo Vieira de [Music] Olivera in Brazil doctors were shocked when a baby was born with a head turned up upside down and severely disfigured limbs despite medical advice urging the parents to withhold nourishment they defied the advice of the Specialists and chose to conceal their child's [Music] disability and years later the child turned out to be an accountant and embarked on International Journeys delivering motivational speeches however all of this couldn't have been possible without the idea of having paternal support love and guidance his story tells us about the importance of Love regardless of the family going through a hard time Nadia Lorella Nadia Lorella a 26-year-old inspirational athlete from Sicily managed to embark on a motorbike ride as a form of therapy finding the purpose of her life and confidence despite being born with fol Amia syndrome this rare condition results in limb malformations causing the absence or extreme shortening of Bones during birth Nadia has faced Prejudice from strangers but regardless of all the negative comments she has managed to live her life to the fullest discovering the benefits of motorbike therapy for disabled individuals through a YouTube video Nadia found renewed confidence defying the odds now she's been planning routine motorcycle trips to get herself mes memorized by the beauty of the world Mona sing and Sona Singh they were born with one of the rarest medical conditions in the world Sona and Mona sing born with one of the rarest medical conditions share a stomach liver and bladder although their hearts lungs and brains are separate they coexist in a unique physical connection are you feeling this yes you're not feeling it who is feeling this despite this connection Sona and Mona maintain separate identities and express individual preferences do you have separate wallets no single wallet they entertain the idea of marriage with the same person and share common Hobbies do you guys want to marry the same person yes same person same such as playing mobile games on a shared phone the 19-year-old brothers raised by the pingalwara Association after being abandoned in Delhi India navigate life with two legs four arms and a shared identity they perform daily tasks with remarkable coordination including operating an electric vehicle where Mona controls the brake Sona manages the accelerator and they steer together Zion Clark the Foster system said hey we have this kid we're going to throw him out would you take him in born without legs due to a rare condition known as codal regression syndrome Zion has defied expectations to become an accomplished wrestler and motivational speaker through his accomplishments in wrestling and his impactful speeches he continues to break down barriers and motivate others to overcome challenges in their own lives his journey into wrestling began in high school where he not only overcame physical limitations but also emerged as an extraordinary athlete with unmatched determination and a passion for the sport Zion competed at a high level earning victories and inspiring others with his talent Zion's positive attitude and indomitable Spirit have garnered admiration and support I made it here to America's Got talent to show the world that anything is [Applause] possible Nick dism Nick was looked at in the hallways differently it was weird cuz I'm the younger brother but I'd try to be protective of him Nick dmic a social media influencer's life took an unexpected turn when he began noticing unusual swelling on his face after investigations he discovered that he was battling a genetic disease causing the growth of tumors along nerves enduring 100 80 stitches following two surgeries he now faces a pivotal third surgery aiming to alleviate the excess weight on his face determined to raise awareness he courageously shared his journey with his fans he hopes this procedure will contribute to NF1 research this influencer story underscores the resilience needed when confronting an obstacle in life emphasizing the power of sharing experiences to Foster awareness and support for medical conditions most to the surgeries Maybe spread the message I don't know Lindsay Hilton my name is Lindsay Hilton I was born missing both my legs and both of my arms born without limbs despite her physical challenges and facing doubts because of her appearance Lindsay Hilton has become well known on social media for her inspiring Journey as a rugby player and adaptive strength athlete my strong points are things like pulls and body weight exercises Hilton chose to be and competitive from a young age playing sports like soccer swimming rugby and field hockey for Hilton going to the gym is a way to stay healthy be part of a friendly community and eat snacks without gaining too much weight in her 20s she found CrossFit to get stronger for rugby even winning a gym contest in simple words she inspires others to keep going CrossFit contests are notoriously grueling but Lindsay just ranked second work through the paint and not give in to that little voice telling you to stop Abigail and Britany Hensel when I went into the hospital I was expecting one child they realize that they were conjoined twins Abigail and Britney Hensel born in 1990 embody an exceptionally rare case of conjoined twins with two distinct heads sharing a single body and vital organs remarkably each twin independently controls one arm and one leg necessitating coordinated efforts in their daily tasks with unwavering family support they successfully navigated School completed their education and now they work as instructors at a school their unity and overcoming challenges serves as an inspiration demonstrating that living a shared life is no longer a hindrance Abigail and Britney have become a beacon of motivation particularly for young children showcasing the notion that with determination anything is achievable Shiloh Pepin some people are short some people are tall look I'm not even quite the same than all the others but some people just like the way I am Shiloh Pepin renowned as Kenna bunk port's mermaid girl was one of three individuals globally living with mermaid syndrome born with fused legs only one partially functioning kidney and lacking a lower colon she defied expectations surviving past the few days initially predicted by doctors Shiloh underwent her first kidney transplant at 2 followed by a second in 2007 after enduring 2 years of painful dialysis despite being on the path to recovery she succumbed to pneumonia at the age of 10 her parents were told she would only live for days but nature had other plans giving her 10 years on our planet her story touched the hearts of millions Haram cow leave the Guinness World Record for being the youngest woman with a fully grown beard born with polycystic ovary syndrome or PCOS a condition causing excessive hair growth Haram made headlines when she entered the Guinness World Records as the youngest woman with a full beard she had broken the stereotypes about femininity and beauty standards her decision to keep her beard serves as a symbol of empowerment and Defiance against conventional Norms our nfac bullying and discrimination throughout her life I was just sick and tired of all the body shaming and bullying and people not letting me live my life through what I want to instead of succumbing to societal pressures she embraced her unique features and became a powerful advocate for body positivity as a public speaker she shares her personal journey to inspire others to embrace their individuality and challenge preconceived notions of beauty arnam Cowart is now known as a British seek model activist and motivational speaker for challenging societal norms and promoting self-love and acceptance and has helped in creating a better Community for females Isaiah aasta hey how you doing I'm missing a jaw a vocal voice I'm not missing a life born in 1999 in Arizona Isaiah faced a life-altering circumstance early on being born without a jaw despite this rare condition he has emerged as a source of inspiration for many through his unwavering Spirit Isaiah communicates using a text to speech device and his story gained widespread attention when he collaborated with rapper trap house for the song oxygen to fly which sheds light on his experiences and aspirations he wishes to use music as a medium for conveying messages for hope I more so feel that he's a poet he's writing poetry he's talking about his experience Beyond his musical Endeavors Isaiah aasta has become an advocate for those with disabilities working to break down societal barriers and challenge perceptions by being a motivational speaker he encourages others to see beyond physical differences and recognize the shared Humanity that unites us all Lett padar a resilient 17-year-old student from the small village of Nanda in Mia Pradesh has faced a lifetime of challenges due to an extremely rare condition known as Hyper chosis often referred to as werewolf syndrome born with a rare congenital condition known as Hyper chosis this genetic condition results in excessive hair growth all over the body however this is an exceptionally rare condition with only around 50 documented cases since the Middle Ages Lett padar maintains a remarkably positive outlook on life in the face of Relentless bullying he vows to always be happy and keep others happy lett's optimism in the face of such challenges serves as an inspiration to the strength of the human Spirit Luna Fenner South Florida mom whose daughter was born born with a disfiguring and potentially cancerous condition I have the latest on the ongoing effort to remove a Batman birth mark from a little girl's face Luna Fenner was a baby girl from Florida whose birth brought joy to her parents however Luna was born with a rare skin condition known as congenital melanocytic neas presenting as a large birth mark covering her nose and eyelids resembling a Batman mask sadly for Luna she had been the center of ridicule and was called ugly but most people weren't aware that Luna was grappling with a severe form of skin cancer she was born with the giant neous like that birth mark and that can become to a melanoma like a bad cancer in a series of courageous Journeys to Russia with her mother Luna underwent six groundbreaking medical procedures that successfully eliminated her pigmentation giving her a new life and hope for a better future Samuel man we were being told that Samuel would only have a little time possibly after he was born and even if I had just that little time I wanted that with him Samuel man is an 11-year-old boy living through the harsh realities of life with his unshakable smile and High Spirit Samuel has a rare form of dwarfism called thanatophoric dysplasia it's a known fact that his parents were multiple times urged for a therapeutic adoption but they chose to stick with their beautiful child Samuel has his own way of communicating with others and always keeps his smile on his face his parents consider him a gift from the Divine and he's only strengthen their family Samuel has taught the world that every life is worth saving whether there are challenges or not we should never stop celebrating the good things Epiphany a 17-year-old girl living with kyphosis a rare condition that normally occurs in curved spine faces a challenge in the form of bullying she has earned herself the title of the world's thinnest girl despite the hardships in life Epiphany is determined to excel academically using her studies as a form of revenge against those who bully her epiphany's mother a single parent raising seven children struggles to provide for the family's needs an epiphany aspires to become a doctor and plans on advocating for the individuals who have dealing with similar problems on their own she wishes to start an NGO that will help donate for good causes Nick voic it was like a light bulb when you know just flashed in my brain I'm like Hey Now life I see as an opportunity Nick voic is an Australian motivational speaker and author born on December 4th 1982 in Melbourne Australia he gained worldwide recognition for his inspiring story of overcoming Tetra Amelia syndrome a rare disorder characterized by the absence of all four limbs from a young age Nick encountered numerous obstacles and endured bullying but he learned to adapt to his circumstances he started speaking publicly at the age of 19 sharing his views and spreading a message of Hope in addition to his motivational speaking Nick vichich is a successful author having written several books including Life Without Limits and Unstoppable am my life there's hardly anything I found that I can't do Isa Kil Patrick screeton um that she had a condition called mandulo aqual displasia but the mutation that they'd found they'd never seen before Isla is a unique 4-year-old born with a rare mutation called mandibular Aqua dysplasia she's had to face problems like bone growth and premature organs from an early age furthermore it's recorded that she happens to be the only person in the world world with this condition although it puts her life at a significant risk despite having her checked by various doctors her family strives for her to have a normal life Isa along with her sister gained popularity on Tik Tok earning the nickname Benjamin Button due to her premature aging in reference to the famous movie but other than the odd Outlook she happens to be the most Lively person on the inside zenana Ellie in Rwanda a woman who had lost her first five children found solace when Ellie a boy with unique features and learning disabilities was born the boy however depicted unusual characteristics and sadly villagers targeted him calling him bad names due to which he ended up spending a lot of time alone in the woods he also had a strange diet of eating leaves and grass instead of regular food following the viral spread of his story Global contributions poured in to support him and his mother with a newfound assistance Ellie attended school and also learned to communicate and has transformed into a local Superstar Dawning suits and designer clothes Tio satrio Tio satrio is another 15-year-old from West Java Indonesia he defies all the odds with his incredible human Spirit he was born with a rare condition that left him without arms and legs however regardless knowing that he was beyond being normal he didn't give up and instead chose to battle the hardship in his own unique ways he possesses a brilliant mind like he can use a pen with his mouth to write and he also loves football his idea of engaging into sports is through playing video games highlighting passion and adaptability his life is nothing short of a miracle boana danovich when visual information reaches her brain it is processed as an upside down image boana danilovich a 29-year-old from Serbia faces life with a rare neurological condition that causes visual information to be processed upside down in her brain she was diagnosed with spatial orientation phenomenon people normally approach her stating that she's been reading the newspaper upside down while this condition affects certain aspects of her vision she can perceive people normally despite this unique perspective spatial orientation poses challenges including discouragement from obtaining a driver's license and difficulties in education discourage from getting a driving license I had problems at school I could not get the education I wanted boana however hasn't allowed these challenges to hinder her progress working at the local Council she utilizes a special inverted screen and even at home medical science hasn't reached up to the point of identifying what could be the root solution for this issue jat [Music] Kumar jat Kumar an 8-month-old baby girl from Punjab India faced a health condition as she had a weight of 38 lbs which is equivalent to the weight of a 4-year-old the reason for the baby's weight gain is its diet however the medical professionals aren't able to find the probable cause for her disease the baby's excessive weight has led to breathing problems however the parents are still hopeful that one day their daughter will lead a normal life although the father earns limited resources he plans on taking help from the government and other private or state-owned institutions to help his child Byron schlecker my tongue's uh 8. 6 CM wide which is roughly a little more than 2 cm wider than the new iPhone 6 Byron schlecker was born in 1968 he achieved notable recognition for having the world's widest tongue he managed to become significantly widespread across social media this accomplishment had added his name to the 2020 Guinness World Records the total length of his tongue is measured to be at 8. 6 CM he has also been part of online memes however not only Byron but his daughter too also holds the record for whitest tongue for females it does feel a little weird like this is not really something that happens every day they both have a unique bond with each other worthy of being cherished by millions around the world it's always nice to have a world record running within the bloodline huh only the future will tell if another schlecker manages to hold the widest tongue title or not Adrien Lewis hi my name is Adrien Lewis I'm 19 years old I'm from M Michigan this American woman first rose to prominence in 2014 when her impressive tongue measurements went viral Adrien born in 1991 and hailing from Michigan gained attention for her unique talent as she claims to have the world's longest tongue her tongue measures around 4 Ines from the tip to the back of her throat and she showcases her unusual skill through videos and social media while Adrienne Lewis may be best known for her extraordinary tongue length she continues to navigate the online world with a positive outlook as in Beyond her viral Fame and popularity Adrienne has expressed her desire to use her platform to encourage body positivity and mental health awareness she promotes embracing one's unique qualities and challenging societal Norms congratulations Jeff da let's start with this let's turn so the camera can see my hand versus your hand hailing from Stacy Minnesota Jeff Dave was born in 1963 he's an arm wrestling competitor known for his unusually large hands and forearms he gained attention for their extraordinary size likely due to a condition called gigantism or acromegaly Dave's unique physical attributes became widely recognized when videos and images of his arm wrestling matches surfaced on social media his massive hands and forearms give him a distinct advantage in arm wrestling competitions despite his Fame in the arm wrestling Community Jeff Dave maintains a lowkey profile and there's limited information available about his personal life it just kind of stayed the same as I grew up I also grew up on a farm so I used to do a lot of farm chores Isaac Johnson I have the biggest mouth in the world Isaac Johnson of the United States managed to secure the Guinness world record for the largest mouth gape measuring at 10196 CM or approximately 4.
1 104 in from top to bottom this is equivalent to the size of a baseball Isaac initially held the record until it was briefly broken by another individual however he managed to reclaim it by extending his mouth another 021 CM Isaac gained widespread recognition amassing over 74 million Tik Tok views solidifying his status as an instant celebrity as he's been called upon numerous shows for portraying his talent f always get astonished to see his wide open [Music] mouth romesa geli it is so R and I am the first case diagnosed in Turkey born on January 1st 1997 romesa gilgi is a Turkish Advocate researcher and web developer gilgi lives in the kabuk province of turkey her height was caused by Weaver syndrome a rare condition which causes r rapid growth among other abnormalities it affects men three times more than women although because of her condition she usually uses a wheelchair to move but can walk for short periods of time with a walker due to this condition she cannot sit in seats under 50 to 55 cm tall on September 28th 2022 gilgi was able to fly on an airplane for the first time in her life Turkish Airlines had to place a stretcher on six chair rows in one of their planes to make her trip from Istanbul who looks theist you you of course Maas schit that's that's a good base but it's small and Maas schit from Halen's leban is a German arm wrestler who was born on April 2nd 1987 with a genetic defect called Clippo tranon Weber syndrome Mathias was born with a more powerful right arm he turned this imbalance to his Advantage though and chose a career as an arm wrestler since 2004 Maas Hellboy schit has been part of the competitive arm wrestling team at vfl wulfsburg after several successes in various amateur tournaments he won the German youth championship in the under 70 kilogram class in his first professional competition his impressive Journey includes undefeated victories in the German championships in 2008 and 2009 leading team north to the Bundesliga Team Championship winning silver at the 2010 German [Music] Championship Sam Burns I'm Sam and I just turned 17 and I have a disease called Progeria it affects only about 350 kids today Sam Burns a remarkable individual left an enduring impact on the world before his passing in 2014 at the age of 17 very sad day 17-year-old Sam Burns being laid to rest today he was born with progeria a rare and Rapid aging disorder Sam became an ambassador for Progeria awareness shedding light on this uncommon condition and fostering hope for affected families Sam's life was an inspiring Testament to resilience and positivity about all the positive things that are around and and uh try to make it better so despite basing physical challenges he embraced life with an infectious enthusiasm that touched Hearts globally Sam story gained prominence through the HBO documentary life according to Sam which chronicled his journey and advocacy efforts his tedx talk My Philosophy for a happy life garnered millions of views encapsulating his wisdom on finding joy in the face of adversity every time I see Sam it's sort of a moment he gets off the bus Mandy C my left leg has continued to grow at rapid pace Mandy entered the world with a genetic anomaly that led to abnormal development in both of her legs resulting in an extraordinary weight of 95 kg just for her lower limbs regardless of the obstacles in her life she chose to lead a life of autonomy relying on tailored supports specially crafted outfits and a customized handrolled vehicle to navigate her surroundings to add to her already complex circumstances Mandy underwent the difficult decision of a surgery striking instead of relieving her from challenges this decision brought forth a new set of complexities as her severed leg began to exhibit an accelerated growth rate in the midst of these trials Mandy maintains an unwavering hope her Story shows how strong she is as she keeps going with courage and a positive attitude I'm hoping to get a wheelchair and one that I can actually push myself around him which is something I've never Kim Goodman people are paying to see this Goodman is now Guinness certified for the world's longest eyeball Kim Goodman holds the Guinness World Record for the farthest eyeball protrusion with an extraordinary and somewhat puzzling Talent she distinguishes herself in a league of her [Music] own Kim can extend her eyeballs beyond the normal human capacity with her eyes popping out of their sockets by an impressive. 47 in this unique feet has captivated audiences globally making her a stand Ed personality Kim's Guinness World Record highlights the breath of extraordinary skills that individuals can possess turning her into a notable figure in the realm of unique and astonishing accomplishments going I have the talent because my I do a squint and they pop out Rodriguez Hernandez Rodriguez Hernandez achieved the Guinness World Record for having the largest feet his right foot measured one 1. 31 ft long however his left foot reached 1.
