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I Fell In Love With My Wife’s Girlfriend | EXTREME LOVE8m27s

I Fell In Love With My Wife’s Girlfriend | EXTREME LOVE

FINDING out your wife is in love with someone else would be cause for divorce for most couples. But when part-time police officer Joey Triplett’s wife Crystal told him that she had fallen for a younger woman, he gave his blessing to their relationship - and set in motion a chain of events that led to the three of them living together in a polyamorous 'triad'. Now Joey, 37, and Crystal, 35, share their lives with 23-year-old Jamie, with their 8-year-old son Jamison even calling her ‘mom’.

Meet The 10-Year-Old CrossFitter Aiming For The Olympics5m21s

Meet The 10-Year-Old CrossFitter Aiming For The Olympics

An amazing 10-year-old girl is weightlifting more than adults twice her age at her CrossFit gym - where she trains up to nine hours a day. Brooklyn Sittner, from Billings, Montana, started weight training at six-years-old after falling in love with the sport at her dad’s gym and can now lift 45 kgs (almost 100 lbs) - the equivalent weight of a teenage boy. The pint-sized weightlifter set three state records at the Montana State Weightlifting Championships - lifting a combined total of 74 kgs (163 lbs) - and is on her way to dominating at the Youth Nationals in June. Her ultimate goal is to compete in the Olympics when she turns 14. Her love for the sport developed when she set eyes on the rings. She would try to pull herself up on and on and nowadays she does it with an extreme ease. She is highly competitive and doesn’t mind challenging others twice her size and triple her age. She takes them on and wins almost every time. Even her father admits that she has mastered the sport to a point where now she is the one training him. Brooklyn is very happy doing what she does. She says that this way of living is giving her a purpose, and she wouldn’t have it any other way. She has dedicated a lot of her time to CrossFit, training 6 or 7 days a week and getting homeschooled so that she would have more time to do what she really loves. She admits that one of her favorite things about it is that she can travel a lot, something that her peers aren’t able to do.

I Have Half A Body | BORN DIFFERENT6m08s

I Have Half A Body | BORN DIFFERENT

DESPITE living with just half a body – inspirational Rowdy Burton is determined to not let his condition define him. 30-year-old, Rowdy, was born with a rare lower spinal disorder called Sacral Agenesis. Affecting only one in 25,000 births, the condition resulted in Rowdy having both of his legs amputated when he was just three years old – with doctors using pins to stop his bones growing any further. Rowdy, who resides in Alabama, USA, was left to live his life with two stumps positioned directly beneath his waist and now that he is older, he prefers to use his hands and elbows to get around rather than a wheelchair. After all the hardship Rowdy has faced over the years, he is still determined to live his life to the full – playing tennis with his friends and riding his skateboard.

Man Has His Hand Sewn Inside His Stomach In A Groundbreaking Surgery3m48s

Man Has His Hand Sewn Inside His Stomach In A Groundbreaking Surgery

A man whose hand was saved after it was sewed inside his abdomen is now set to have pioneering surgery, the first of its kind in the world, to restore full use of his fingers. Former machine operator Carlos Mariotti, 43, from São Ludgero in southern Brazil, lost all the skin from his hand and fingers in a horrific workplace accident in March 2016. However, quick-thinking surgeons decided that rather than amputate, they could salvage the totally mutilated hand by surgically tucking it into a soft-tissue pouch in his belly, where it stayed for 42 days. The doctor had never done that type of surgery and he had never seen it performed before. Carlos had two more surgeries in May 2016, which left his hand looking like a boxing glove, and despite of its gruesome appearance, he is lucky to have a hand at all. He had to remember every day that he cannot take his hand out of his body, which is a really strange sensation. Now, he is set to have two more procedures to radically improve the range of movement in his hand, by separating his fingers and repairing his nerves. He has not been able to work since the injury, but he started to pick up things and exercise, making small improvements, and now faces a financial battle to raise money for the surgery . Videographer / director: Janet Tappin Coelho Producer: Tom Midlane, Ruby Coote Editor: Joshua Douglas

Real Life Vampires Find Love At First Bite: EXTREME LOVE5m05s

Real Life Vampires Find Love At First Bite: EXTREME LOVE

When fetish model Lea met tarot-reader Tim, it was love at first bite. The 20-year-old fanged beauty and the 31-year-old psychic are real-life ‘vampires’, from Austin, Texas, who have a passionate relationship based on sucking each other’s blood – and say it’s better than sex. ‘Countess Lea of House Van Doorn’ and ‘Count Tim of House Van Doorn’ met two years ago at a vampire festival and felt an instant ‘connection of darkness’, which quickly developed into a blood-sucking relationship. Now the pair, who care for Tim’s three-year-old son, Daedric, are planning to tie the knot in a vampire themed wedding ceremony next year. These people don’t have the supernatural abilities that we associate with the likes of Dracula, but are rather individuals who claim that they have a condition which requires them to drink blood for sustenance. Videographer / director: Ruaridh Connellan Producer: Emma Pearson, Ruby Coote Editor: James Thorne

I Want The World’s Biggest Hips Even If It Kills Me: HOOKED ON THE LOOK3m36s

I Want The World’s Biggest Hips Even If It Kills Me: HOOKED ON THE LOOK

Bobbi-Jo Westley is on a one-woman quest to have the world’s biggest hips - even if doing so KILLS her. Currently measuring 95 inches, she has her sights firmly set on the current record of 99 inches, held by LA-based Mikel Ruffinelli. And her supersized hips have already earned her a supersized following, with legions of fans from around the globe buying and trading her pictures online. Despite the warnings of doctors and nutritionists that her current lifestyle means she is a ‘ticking time bomb’, she is determined to keep on growing her hips until she sets a new world record - or die trying. Her super-sized hips have already garnered her a super-sized following; her fans are actually collecting and trading with her pictures online. They don't stop at pictures; people actually pay money for the New Yorker to sit on them and squash them. The dark side of her over-sized fame is that Bobbi-Jo is constantly on the sharp end of the hateful messages from Internet trolls. This doesn't make her want to quit though; in fact, she thinks that her hips are what makes her unique. "I want to be remembered for something, and I think having the world’s biggest hips is what I was meant to be remembered for.” says the SSBBW, which stands for “super sized big beautiful woman” Videographer / director: Carlos Chiossone Producer: Tom Midlane, Ruby Coote Editor: Marcus Cooper

700lb BBW to 465lb Proud Mum | HOOKED ON THE LOOK7m53s

700lb BBW to 465lb Proud Mum | HOOKED ON THE LOOK

WHEREAS she once drank 3,500 calorie milkshakes through a funnel to intentionally gain weight, new mum Monica Riley has now swapped funnel feeds for bottle feeds. Dining out on up to 10,000 calories a day, Monica Riley, 29, of Fort Worth, Texas, dreamed of being the fattest woman in the world and of being “immobile”. She ballooned to over 700lbs and set her sights on becoming so large that she would be bedbound, but the 29-year-old decided to change her life – and her body – after discovering she was pregnant in March 2017. Determined to ensure a healthy pregnancy after two previous miscarriages, Monica dropped to 520lbs through healthy eating and gentle exercise, and gave birth to baby Michelle in October 2017 by C-section. Though Michelle initially had trouble breathing and had to be kept in hospital for observation for six weeks due to reflex and four small holes in her heart, she is now back home with her besotted parents, and Monica is now planning gastric bypass surgery in a bid to lose even more weight.

Model Promotes Psoriasis Positivity | SHAKE MY BEAUTY5m30s

Model Promotes Psoriasis Positivity | SHAKE MY BEAUTY

A YOUNG model is spreading a message of body positivity by embracing the severe skin condition that at one point left 90% of her entire body covered with painful scabs. Celia Martinez from Guadix, Spain, was diagnosed with psoriasis aged 16 when she discovered small red dots on her stomach that eventually spread everywhere, including parts of her face. But rather than airbrushing or Photoshopping away her imperfections, Celia has amassed an online following of more than 10,000 followers on Instagram by confidently displaying some of her worst outbreaks to help encourage others to be comfortable in their own skin.

Disabled Sisters Are Queens Of Beauty Pageant | BORN DIFFERENT8m30s

Disabled Sisters Are Queens Of Beauty Pageant | BORN DIFFERENT

THE world of beauty pageants has helped two disabled sisters find their confidence and, for one of them, her first words. From a young age, both Ava, 9, and 4-year-old Jessa struggled with their confidence, with Jessa unable to speak at all. Ava was born with achondroplasia, the most common form of dwarfism, and Jessa has spina bifida milamidiseal - one of the most complex forms of spina bifida. Parents Jacqueline and Jason Whipple turned to beauty pageants to see if they could bring the girls out of their shells. Between them, Ava and Jessa have appeared in 40 beauty pageants, winning several crowns along the way, not to mention the hearts of everyone who meets them - and their parents couldn’t be prouder.

Woman With Past Eating Disorders Inspires Others To Start A Recovery8m07s

Woman With Past Eating Disorders Inspires Others To Start A Recovery

This is the emotional story of a 28-year-old woman, whose weight dropped to 88lbs due to her eating disorders, leaving her with anorexia and bulimia. She decided to share her story with the world and show other sufferers that recovery is indeed possible. Listen to her inspirational story! Meet Lindsey Hall, from Fort Worth, Texas, whose teenage eating disorders caused her serious health problems, leaving her struggling with anorexia and bulimia. She would drink wine on an empty stomach just to curb her appetite. How horrible! Four years ago Lindsey went to an eating disorder treatment centre and is now still in recovery, which according to her is a process that will last for the rest of her life. In addition, she writes about her recovery on her blog ‘I Haven’t Shaved In 6 Weeks’, trying to inspire others who are struggling with eating disorders to seek treatment and feel better. Lindsey, now lives in Denver, Colorado, and doesn’t think that anybody ever fully recovers from eating disorders . She will have to live with it and fight against this awful health condition for the rest of her life. It is interesting that this condition develops early in life, and it is boosted by the unhealthy eating habits . Lindsey explains that even as a child, her relationship with food ‘was always tumultuous’. She restrained herself from certain foods and ate only about 12 or 14 items of food. She fancies French fries, breakfast food, waffles, oatmeal, eggs and cereal. Can you imagine living on these foods only, for the rest of your life? Surprisingly, these early eating patterns weren’t about counting calories and carbs, but sure contributed for Lindsey to establish a distorted relationship with food throughout the teen and adult years. The cycle of food restriction and bulimia continued throughout the years. Alongside her exercise addiction, Lindsey was suppressing her hunger by drinking. When Lindsey started drinking alcohol to mask her appetite her condition was referred to as drunkorexia which refers to those who save all their calories for binges. However, she knew she had a problem and agreed to spend six weeks as an inpatient at the Renfrew clinic in Florida and continue as an outpatient at the Renfrew Centre in Dallas. She now exercises and eats in moderation and blogs and speaks publicly about her recovery journey in an attempt to inspire others to do the same and tackle this disease.

Car Crash Scars Won’t Kill My Modelling Dreams | SHAKE MY BEAUTY6m29s

Car Crash Scars Won’t Kill My Modelling Dreams | SHAKE MY BEAUTY

A TENACIOUS model has learnt to show-off her scars after a tragic car accident left her fearing for her future. When she was just 23 years old, Neli Zuma was fighting for her life in ICU with internal bleeding after her friend’s car span out of control and hit a wall. Neli, now 25, was left with a gaping hole in her stomach and doctors had no choice but to remove skin from her thigh and sew it to the open wound to prevent her bleeding out. Unfortunately, there was nothing they could do for her close friend who passed away two days later. Neli, who had just started out with her modelling career, was left with unusual scarring on her stomach and thigh and she had to use a colostomy bag for 10 months. Her body-confidence had hit an all-time low. But after months of trying to improve the way she saw herself, Neli from Durban, South Africa, decided it was time to show the world that she is no longer ashamed of her scars.

This Fitness Fanatic Won't Let Her Brittle Bones Stop Her5m31s

This Fitness Fanatic Won't Let Her Brittle Bones Stop Her

She is young and brimming with vigor - and she won’t let her brittle bone condition get in the way of her fitness goals! Jasmine Manuel is only 22 years old, but she suffers from Osteogenesis Imperfecta Type 3, a severe type of disorder of the bones, making them incredibly susceptible to fractures. That is the reason why she is much shorter than other women her age. The severely brittle bones are not her only issue. Jasmine also suffers from severe scoliosis and has to move around in a power chair. But the fitness fanatic, who is also a student at Kennesaw State University and produces music under the pseudonym “Mini Producer”, uses her condition and stoic mental attitude to advocate for disabled fitness. “I like working out because it’s proving that I can do it. A lot of doctors have said different things about what I was going to be capable of, and every day I am just proving that I got this. I can do whatever.” Jasmine says. “I don’t have time to pity myself because there is nothing to feel sorry for, this is what it is… I don’t really have a choice but to be positive and live my life.” The heroine says she has broken anywhere between 100 and 200 bones in her lifetime and has undergone 22 surgeries. Still, these setbacks have not slowed her down - she has even taken on Fitness guru Shaun T’s Insanity Max 30 workout regimen. Her program has her doing push-ups , crunches and using all sorts of gym equipment on her university campus. She admits she was just curious if she could do it. But after seeing how she could work out without her bones breaking, she kept persevering and now has even started training another woman who is also in a chair, which she says gives her a great sense of pride.

I Won’t Hide My Vitiligo With Makeup | SHAKE MY BEAUTY7m07s

I Won’t Hide My Vitiligo With Makeup | SHAKE MY BEAUTY

A STUDENT has finally embraced her vitiligo after years spending hundreds of dollars a month on make-up to disguise it. Up until a year ago, 21-year-old Mariah Perkins, from Timonium, Maryland, would hide the white patches on her face with thick make-up. Vitiligo is caused by a lack of the pigment melanin and the criminology student would spend hundreds of dollars a month on her heavy-duty foundations. By the time she got to college she would even sleep in her make-up. But a year ago Mariah grew tired of caking her face in foundation and decided to go “cold turkey”. Posting pictures of her natural beauty on social media, Mariah was amazed by the positive comments and finally stopped disguising her vitiligo with make-up, even when performing with her dance group.

Couple Build World’s Biggest Bunny Collection5m33s

Couple Build World’s Biggest Bunny Collection

A MARRIED couple have demonstrated their undying love by amassing the world’s biggest bunny collection. And their colony of rabbits has grown so vast they’ve housed it in a museum. Located in Altadena in Los Angeles, The Bunny Museum is a huge collection of more than 35,000 items of bunny memorabilia which tell a decades-long love story. The museum was co-founded by husband and wife team Candace Frazee and Steve Lubanski, and includes rabbit-related art, literature, figurines, games, and even Candace and Steve’s former real-life bunnies, who have been taxidermied and preserved for future visitors to enjoy.

Brazilian Woman Is Using Her Unique Birthmark To Launch Her Modelling Career6m06s

Brazilian Woman Is Using Her Unique Birthmark To Launch Her Modelling Career

Mariana Mendes, 24, was born with congenital melanocytic nevus, a type of birthmark that occurs in an estimated one percent of infants worldwide. Mariana’s unmissable birthmark covers the center of her face and, while many struggle to accept their birthmarks, Mariana has always fully embraced hers and encouraged others to do the same. Instead of being ashamed of the way one looks, they have to be fully aware of their ‘drawbacks’ and turn them into something powerful to make them feel special and unique. Because everybody is beautiful in their own way and this is just a different kind of beauty. As she says women do not need to fit into conventional beauty standards to be models. Neither do they have to be thin and tall with all the characteristics that the media now demands. Everyone has their own type of beauty even if you have characteristics out of the normal beauty standard, that’s your own kind of beauty. People have to accept themselves as they we are. And that is the only standard. This brave woman has chosen not to cover it up and she never uses makeup to do that because she knows that the birthmark is part of her and part of her personality. She has also never considered removing it. Now Mariana works mostly as a print model for clothing designers and she has launched a career as a digital influencer with 21,000 Instagram followers.The Brazilian beauty hopes her boldness will help break down barriers in the fashion industry and inspire more people to proudly bare their birthmarks.

The Boy Who Can’t Stop Hurting Himself | BORN DIFFERENT8m30s

The Boy Who Can’t Stop Hurting Himself | BORN DIFFERENT

A young boy faces a daily battle with a rare condition which causes him to severely injure himself. Davey Wicklund, 11, from Renton, Washington, has a rare inherited disorder that affects his muscle control called Lesch Nyhan syndrome. Davey’s mother, Jaren explained: "Lesch Nyhan syndrome is basically cerebral palsy with self injury. Davey has got the extreme. He cannot stand, walk, he cannot pull his head up for long time, independently. He has got the muscle strength, but not the ability to control.” The parents have to take special measures daily to ensure that Davey doesn’t hurt himself; including arm braces, kangaroo-type pouches to tuck his legs in and a rubber mouth contraception to stop him biting his lip.

Father Finds Happiness After Suicide Attempt8m49s

Father Finds Happiness After Suicide Attempt

A MAN who tried to take his own life has finally found recovery after battling depression for years without a diagnosis, beginning his own mental health charity in the process. For Pat Lawson, growing up with depression wasn’t something he so much tried to hide as something he wasn’t even fully aware of. It wasn’t until he attempted suicide, age 30, that Pat sought the medical help he’d needed for so long - and finally shared with others the depression he had been battling alone all his life. The 32-year-old father of two, from Australia, set up an online group and charity to support men with mental illnesses called Three Words, named after the three most important words anyone with a mental illness can say: ‘I need help’.

Father Finds Happiness After Suicide Attempt8m49s

Father Finds Happiness After Suicide Attempt

A MAN who tried to take his own life has finally found recovery after battling depression for years without a diagnosis, beginning his own mental health charity in the process. For Pat Lawson, growing up with depression wasn’t something he so much tried to hide as something he wasn’t even fully aware of. It wasn’t until he attempted suicide, age 30, that Pat sought the medical help he’d needed for so long - and finally shared with others the depression he had been battling alone all his life. The 32-year-old father of two, from Australia, set up an online group and charity to support men with mental illnesses called Three Words, named after the three most important words anyone with a mental illness can say: ‘I need help’.

700lb BBW to 465lb Proud Mum | HOOKED ON THE LOOK7m53s

700lb BBW to 465lb Proud Mum | HOOKED ON THE LOOK

WHEREAS she once drank 3,500 calorie milkshakes through a funnel to intentionally gain weight, new mum Monica Riley has now swapped funnel feeds for bottle feeds. Dining out on up to 10,000 calories a day, Monica Riley, 29, of Fort Worth, Texas, dreamed of being the fattest woman in the world and of being “immobile”. She ballooned to over 700lbs and set her sights on becoming so large that she would be bedbound, but the 29-year-old decided to change her life – and her body – after discovering she was pregnant in March 2017. Determined to ensure a healthy pregnancy after two previous miscarriages, Monica dropped to 520lbs through healthy eating and gentle exercise, and gave birth to baby Michelle in October 2017 by C-section. Though Michelle initially had trouble breathing and had to be kept in hospital for observation for six weeks due to reflex and four small holes in her heart, she is now back home with her besotted parents, and Monica is now planning gastric bypass surgery in a bid to lose even more weight.

The Bodybuilder With Butterfly Skin | BORN DIFFERENT7m19s

The Bodybuilder With Butterfly Skin | BORN DIFFERENT

A SEVERE skin condition hasn’t stopped one man from becoming a bodybuilder and motivational speaker, despite doctors initially saying he wouldn’t live past the age of five. Dean Clifford, now 38, has become the oldest living survivor in the world of the most serious form of Epidermolysis Bullosa. The genetic condition causes the Queensland-native to have incredibly fragile skin, which blisters frequently and takes much longer than usual to heal itself. Despite this, Dean has transformed himself from a physically weak and sick child to a practiced bodybuilder with a successful motivational speaking business.

My Rare Dwarfism Makes Me 1 in 4 Million | BORN DIFFERENT9m05s

My Rare Dwarfism Makes Me 1 in 4 Million | BORN DIFFERENT

A LOVEABLE 8-year-old boy has a form of dwarfism so rare he is believed to be one of only 28 cases in the world. Three-foot-tall Landen Johnson, from Lincolnton, North Carolina, has primordial dwarfism, one of the rarest forms of dwarfism in the world, with experts estimating there are less than 100 cases worldwide. But Landen’s specific form of primordial dwarfism, DNA Ligase four deficiency or Ligase 4 deficiency, which also affects the immune system, makes him even rarer: his family say they know of only 28 other cases worldwide. Five months after having a bone marrow transplant Landen still has to go to hospital three times a week, can barely go outside and has to take multiple medications – but Landen’s spirit remains unbreakable.

Barbie Wannabe Has Eye Surgery To Look More Caucasian | HOOKED ON THE LOOK8m48s

Barbie Wannabe Has Eye Surgery To Look More Caucasian | HOOKED ON THE LOOK

A SELF-proclaimed ‘human doll’ has had eyelid surgery to make her appear more Caucasian - like her style icon Barbie. Ophelia Vanity, from Los Angeles, California, is half-Chinese by heritage - but spent $4,000 on a blepharoplasty to give her a higher, more western-looking eyelid crease and so more closely resemble the iconic western-looking fashion doll. The 30-year-old, who is half Chinese, has spent over $35,000 on achieving her doll-like appearance and is now planning further surgeries, including implants in her breasts and bum.

Rodrigo Alves Has FOUR Ribs Removed | HOOKED ON THE LOOK9m15s

Rodrigo Alves Has FOUR Ribs Removed | HOOKED ON THE LOOK

Rodrigo Alves has lost five inches off his waistline thanks to his controversial rib removal procedure - and he is hoping to shrink to a tiny 20-inch waist - if he keeps wearing corsets. The 34-year-old plastic surgery addict claims he had the $28,000 procedure not to match any conventional standards of beauty but so that he can look even more unique. Thanks to his rib removal surgery - where he had four floating ribs removed - and constant corset wearing Rodrigo, who has been dubbed the Human Ken Doll, has dropped from a 34 inch waist to 29 inches. Rodrigo finally has the coveted silhouette he’s wanted for so long – but admits he needs to wear a corset 24 hours a day to maintain his hour glass curves.

Boy Born With No Eyes Is Living His Life To The Fullest7m59s

Boy Born With No Eyes Is Living His Life To The Fullest

A mother and her inspiring six-year-old son who was born with a gap in his face is raising awareness of the treatment of people with facial differences. Christian Buchanan from Woodbury, Tennessee, was born with Tessier cleft lip and palate , a rare condition which has only been documented 60 times in medical history. Tessier cleft lip and palate is the result of the facial tissues not joining properly during development, causing a facial disfigurement and the inability to eat, speak and see. Lacey Buchanan from Woodbury, Tennessee shares the incredible story of her son Christian who was born different . The mother of two explains that her disabled child loves to wrestle with his younger brother, he is learning how to play the violin, he is taking karate lessons and he is mastering the sign reading technique. The biggest way this condition affects Christian’s life is his vision impairment, because he is completely blind and he has to learn to navigate the world in the dark. This boy is a real fighter, he has had seven surgeries so far, three reconstructive surgeries on his face to help close the gaps that the cleft left, so that he is able to speak and eat properly. He is going to have a lot more surgeries in the future, because that’s just the nature of his condition. There is a huge social stigma about being different, looking different that most people don’t know how to handle somebody with that kind of difference, or how to be around them. His mom describes Christian as one very independent little boy, he is curious and he likes to explore the world, and he is not afraid to do it. This mom wanted to share her family story in order to raise awareness for disabilities in general and specifically facial differences. She doesn’t want to hid her child, she wants him to be out in the world, he deserves to indulge in all things life can offer. Over the years Christian has grown independent and fearless, and we hope that he learns how to navigate through life properly. We support this brave fighter, good job buddy!

Twins With Albinism Wear Their Condition With Style | SHAKE MY BEAUTY5m56s

Twins With Albinism Wear Their Condition With Style | SHAKE MY BEAUTY

Fashion-obsessed twins who both have albinism want to inspire people to be proud of the skin they were born in. The chances of a child being born with albinism are one in 17,000 - but the chances of twins being born with albinism is far rarer - the odds are not even known. Identical twins Rosemary and Christina Alubankudi, from New York City, are part of this rare club. The 24-year-olds were born with the rare genetic condition, which is caused by a partial or complete lack of melanin, the pigment, which gives hair, skin and eyes their colour. The sisters aren’t just twins, they are best friends too and through their love of fashion, they want to inspire others to be proud of who they are.