Inspiring: People with Disabilities News ArticlesExcerpts of key news articles on
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Special Olympics athlete Chris Nikic crossed the finish line on Saturday to become the first person with Down syndrome to complete an Ironman triathlon. Guiness World Records recognized Nikic's achievement after he finished a 2.4-mile swim, a 112-mile bike ride and a 26.2-marathon run at the Ironman Florida competition in Panama City Beach. "Ironman. Goal set and achieve," said Nikic in a post to Instagram. "Time to set a new and Bigger Goal for 2021." Nikic completed the race in 16 hours 46 minutes and 9 seconds - 14 minutes under the 17-hour cutoff time. Nikic fell off his bike and was attacked by ants at a nutrition stop, but he pushed on to finish the competition. "We are beyond inspired, and your accomplishment is a defining moment in Ironman history that can never be taken away from you," the Ironman Triathlon organization said. Nikic and his father Nik developed the "1 percent better challenge" to stay motivated during training. The idea is to promote Down syndrome awareness while achieving 1% improvement each day, according to Nikic's website. "To Chris, this race was more than just a finish line and celebration of victory," Nik Nikic said. "Ironman has served as his platform to become one step closer to his goal of living a life of inclusion and leadership." Nikic's accomplishment earned him congratulatory messages from celebrities, such as tennis great Billie Jean King and runner Kara Goucher, and people around the world, including 33,000 new followers on social media
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A Chilean start-up has been launched to open up some of the world's most iconic tourist attractions to disabled visitors. The idea for Wheel the World was borne out of an expedition three years ago to Chile's Torres del Paine National Park in Patagonia by a group of friends from the University of California at Berkeley. The group crowd-funded a special wheelchair for their friend, Ălvaro Silberstein, who was left quadriplegic following a car accident when he was 18. They documented their trip [and] began investigating other bucket-list vacations that could be adapted for the disabled. Since its inception last year, Wheel the World's seven-man team has arranged trips for more 900 people, including to Chile's driest desert, San Pedro de Atacama, scuba diving off Easter Island in the Pacific Ocean, ziplining in Costa Rica and a trek along the Inca Trail to Peru's Machu Picchu. Today, the group has 16 destinations both in Chile and four other countries on its online platform, and aims to increase that to 150 by 2020. Silberstein, the firm's chief executive, said the Patagonian trip had made him realize that nothing was impossible. "We realized that with the right equipment and the right information, we can help people with disabilities have these kind of experiences, to open their minds to see that we are capable of anything," he said. "There are many initiatives to make tourism more accessible ... but no one is doing it on a global level, matching tourism services with the specific needs of disabled people. That's what we do," he said.
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On Sunday night, Ali Stroker became the first person who uses a wheelchair to win a Tony Award. “This award is for every kid who is watching tonight who has a disability, who has a limitation or a challenge, who has been waiting to see themselves represented in this arena — you are,” Ms. Stroker said while accepting her statuette for her role as Ado Annie in the Broadway revival of the musical “Oklahoma!.” Ms. Stroker, a 31-year-old New Jersey native who lost the use of her legs in a car accident when she was 2 years old, also thanked her parents “for teaching me to use my gifts to help people.” Ms. Stroker accepted the award, for best featured actress, shortly after dazzling the audience with her saucy performance of the “Oklahoma!” song “I Cain’t Say No.” “I find it to be fascinating that often people don’t think I can dance,” she said. “Who says that dance isn’t turning on wheels? Who says dancing isn’t throwing your arms up in the air and grabbing someone else’s arms to be propelled across the stage?” She also spoke about what it is like to aspire to succeed in an industry where people with disabilities are not represented. “I’m very aware that when I was a little girl I wasn’t seeing anybody like me, and on days when I’m exhausted or discouraged about something, that lights a fire,” she said. “I hope that for young people in chairs who feel that this is too hard, that they see that being in a chair is like getting a secret key to an unknown door — that they ... are reassured that anything is possible.”
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The stand-up comedian Maysoon Zayid likes to joke that if there were a competition called the Oppression Olympics, she would win gold. “I’m Palestinian, Muslim, I’m a woman of color, I’m disabled,” Zayid, who has cerebral palsy, tells audiences, before pausing a beat to hang her head, her long dark hair curtaining her face, “and I live in New Jersey.” The joke lands laughs whether Zayid tells it in red states or blue. She told it near the beginning of her 2014 TED Talk, which drew nearly 15 million views. She now has a development deal with ABC to create a ... sitcom called “Can-Can,” starring her. If “Can-Can” makes it ... it may push two populations, one widely ignored, the other demonized, from the country’s margins into the mainstream. People with disabilities make up nearly 20 percent of the population yet account for about 2 percent of onscreen characters, some 95 percent of which are played by able-bodied stars. And it is hard to imagine a group more vilified in the United States than Muslims or Middle Easterners. Zayid is a vociferous part of a small, dedicated movement calling attention to disability rights in entertainment, which are consistently overlooked in the quote-unquote diversity conversation. Jay Ruderman, president of the Ruderman Family Foundation, a philanthropic and advocacy organization for disability rights ... said Zayid’s show could crush enduring stigmas disabled people face.
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[Otto] Baxter, 31, is part of an art collective called Culture Device — a group of approximately 12 performers that experiment with contemporary dance and theater, pushing the boundaries of the cultural arena by changing perceptions of what it means to be an artist today. This is because of the sheer talent radiating from the small troupe’s repertoire, one that has tackled the likes of haute couture photography and stage classics such as "Waiting for Godot," but also on account that all the performers share the genetic condition Down syndrome. “The starting point is the art,” Daniel Vais, Culture Device’s creative director and choreographer, told NBC News. “Before Down’s syndrome, before extra chromosome, before disability, before anything.” Culture Device has slowly built up a reputation for its high-quality work in a sector not known for its inclusivity. A 2018 report by Arts Council England, for instance, found that most art forms and institutions generally had less than 5 percent of disabled persons working in them. “I didn’t plan to work with artists with Down’s syndrome,” said Vais. “It found me.” While considered a disability that has varying levels of severity, Vais dismisses what he calls a bias-ridden label, preferring to uphold the notion that individuals with Down syndrome have a mindset akin to what’s needed for outstanding artistic creation. “I use improvisation in all of my choreography,” he said, “and artists with Down syndrome are the masters of improvisation.”
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The newest resident of "Sesame Street" has orange hair and a fondness for her toy rabbit. She also has autism. Julia has been a part of the "Sesame Street" family via its storybooks and was so popular that the decision was made to add the character to the TV series. "I think the big discussion right at the start was, 'How do we do this? How do we talk about autism?,'" one of the show's writers, Christine Ferraro, told "60 Minutes" correspondent Lesley Stahl. Over the almost five decades "Sesame Street" has been on the air, it has established a reputation for inclusion with its characters. Joan Ganz Cooney, one of the founders of the Children's Television Workshop which developed "Sesame Street," said it has also not been afraid to deal with real life issues. Julia's debut episode will deal with what autism can look like. The brain disorder can make it difficult for people with autism to communicate with and relate to others. The character of Big Bird talked to Stahl about his first interaction with Julia in which she ignored him. "I thought that maybe she didn't like me," he said. "Yeah, but you know, we had to explain to Big Bird that Julia likes Big Bird," the Elmo character added. "It's just that Julia has autism. So sometimes it takes her a little longer to do things." Ferraro hopes that along with educating viewers about autism the new character will settle in as a part of the neighborhood. "I would love her to be not Julia, the kid on Sesame Street who has autism," the writer said. "I would like her to be just Julia."
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Andrew Short lives with spastic cerebral palsy, which he contracted during birth. Cerebral palsy is a disorder that effects muscle tone, movement and motor skills, but despite impaired speech Andrew’s disability doesn’t impair his mind, and he learned to read early. “I speak three languages,” said Andy. “English, German, and spastic. Spastic is my mother tongue." Andrew is currently completing a Masters Degree in Disability Studies, but his most impressive achievement has been walking the Kokoda Trail, which he describes as “the toughest physical challenge of [his] life”. In Andy’s late twenties, his motor function appeared to begin deteriorating. “We were told to accept that that's what it would be,” said [Andrew's father] David. Instead, David and Andrew began researching the emerging field of neuroplasticity ... inspired by the seminal [book], “The Brain That Changes Itself: Stories of Personal Triumph from the Frontiers of Brain Science”. Andrew’s physical condition is due in part to his trainer, Lee Campbell, a former army trainer and Sydney Swans team member. The two have been training together for five and a half years, and in that time Lee estimates that his physical condition has risen from 2.5 to a 7 or 8. “You watch Andy pull a sled with 20 or 30 kilos of weights in it, he stands up, his posture is corrected,” said Lee. “His finer motor skills now are getting refined. He can hold things, he can cook, he can do his buttons up.” Right now, they’re training together for Andy’s next endeavour, walking the Great Wall of China.
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People always say to me, Anyone who runs as much as you do deserves to be skinny. Of course, what they're really saying: If you do all this running, why are you still so fat? Early that morning [Mirna] Valerio had led a three-mile group run around the campus of Rabun Gap-Na-coochee School in the nearby town of Rabun Gap, where she serves as Spanish teacher, choir director, and head coach of the cross-country team. She's about to start her second run of the day. Every run, every race, every traverse of a mountain trail, every gym workout, Valerio begins by taking a photo. To prove that I was out here, she explains. Later, she will post the photos on ... her blog, Fat Girl Running, in which she both writes of the joys of the running life and thoughtfully, humorously, and sometimes angrily rebuts her doubters, who can't believe that a self-described fat person might discover - or deserve - this kind of joy. With a BMI ... above the National Institutes of Health-established line defining obesity, Valerio, a marathoner, ultramarathoner, and trail runner, has emerged as ... a living argument that it's possible to be both fit and fat. I'm pretty much in love with my body, she writes. Sometimes I get disappointed or angry with it, but like any long-term, committed relationship, it usually comes right back to love and respect. By making peace with her obesity - or, more accurately, by fighting her disease to a kind of enduring, vigorously active truce - Valerio draws kudos from a formerly skeptical medical community.
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The fact that Richie Parker can ride a bike doesn't sound impressive -- until you see him do it. Same goes for the car repairs he makes using power tools. Parker was born without arms, a disability he's overcome time and time again, ultimately leading him to his job engineering chassis and body components for Hendrick Motorsports, NASCAR's most winning organization. "Based on his resume, I knew he could do the things that I needed him to do, it was more a question of how,” Rex Stump, engineering manager at Hendrick, said of Parker. Just like every other hurdle in his life, Parker found a way, placing the keyboard and mouse on the floor, then operating both with his feet to build custom high-performance automotive parts. His story has also inspired countless others, not the least of [whom] is Magic Johnson. After watching [an] ESPN segment [on Parker], the retired NBA star tweeted, "Richie Parker's story proves that you can do anything you set your mind to. We should all stop complaining and giving excuses." Or, as Parker says, "I don't know there's a lot in life ... that I'd say I can't do. Just things I haven't done yet."
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When Jacob Barnett was 2 years old, he was diagnosed with moderate to severe autism. Doctors told his parents that the boy would likely never talk or read and would probably be forever unable to independently manage basic daily activities like tying his shoe laces. But they were sorely, extraordinarily mistaken. Today, Barnett -- now 14 -- is a Master's student, on his way to earning a PhD in quantum physics. The teen, who boasts an IQ of 170, has already been tipped to one day win the Nobel Prize. Since enrolling at Indiana University-Purdue University Indianapolis (IUPUI) at the age of 10, Barnett has flourished -- astounding his professors, peers and family with his spectacular intelligence. The teen tutors other college students in subjects like calculus and is a published scientific researcher, with an IQ that is believed to be higher than that of Albert Einstein. In fact, according to a 2011 TIME report, Barnett, who frequently tops his college classes, has asserted that he may one day disprove Einstein's Theory of Relativity. Outside of his rigorous university commitments, Barnett, who has Asperger's Syndrome, is also an entrepreneur and aspiring author. The teen, who, with his family, runs a charity called Jacob's Place for kids on the spectrum, has used his story to raise awareness and dispel myths about autism. In April, [his mother] Kristine Barnett's memoir about her family's experience with autism, The Spark: A Mother's Story of Nurturing Genius, was released. A movie deal is said to be in the works.
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You've heard of the Rockettes, but have you heard of the Rollettes – a dance troupe of women in wheelchairs? The Los Angeles-based group was founded by Chelsie Hill, who always wanted to be a dancer, and wasn't going to let her paralysis stop her. "In high school, I got into a car with a friend who was drinking and we ended up hitting a tree head-on," Hill [said]. She decided that despite the tragedy, she was going to continue doing what she loved. She danced with her high school team in her wheelchair, and when she graduated, she was inspired to show other girls with disabilities they could dance, too. "I found this group of girls on social media who all had spinal cord injuries and I invited them to my hometown to dance with me. It was such an amazing experience," she said. The group put on a show in Monterey, California, where Hill grew up, and the Rollettes were born. Right now, there are six dancers on the team who perform competitively together. Not only does Hill coordinate this small group of dancers, but every year she holds a dance camp for women around the world. Girls of all ages attend the camp and learn how to dance in their chairs. For Hill, it's not just about teaching others the art of dance, it's about giving them a space where they feel like they belong. "I had a girl say it was the most empowering thing that she rolled into a room and everyone was at eye-level. I want people to come into that room feeling so normal, so empowered so that they can go out in the world and conquer anything," Hill said.
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The crowds that 25-year-old Nick Vujicic draws as an evangelist would have been unimaginable only a few years ago, and impossible had he been born under other circumstances. "In some third world countries ... I would be seen as cursed, a shame to the family," said Vujicic (pronounced VOY-chich). "The possibilities of me being killed at my birth would have been quite high." But Vujicic, who was born without arms or legs, does have one of the most powerful of all human attributes: a voice. Through the ministry he calls Life Without Limbs and a motivational program titled "Attitude is Altitude," Vujicic said he has made 1,600 speaking appearances in 12 nations. "No matter who you are, no matter what you're going through, God knows it," he said. "He is with you. He is going to pull you through." Like all skilled evangelists, he can imagine the deepest vulnerabilities of his listeners, especially among teenage audiences. "I used to think that I needed my circumstance to change before I had any hope," he said. "I wanted to know that there was someone else out there in my position, to know that there is hope, that there is more than just the little box that I see in my life." He cannot avoid the reasons why people are fascinated by his physical condition, and he uses it to his advantage in his speeches, often delivered from a tabletop in front of the audience. He says it lends credibility "to know that somebody has been through something, that they've learned something that you know you need to apply in your own life."
Note: Watch an amazing four-minute video titled "No arms, no legs, no worries," on this inspiring man. Nick has overcome challenges that are almost guaranteed to make your problems seem like nothing.
In 2011, [Ropert Kapen] suffered a brain stem stroke that left him paralyzed. Doctors told his family that he had a 1% chance of survival, and that if he lived, he'd likely be in a vegetative state. Kapen beat those odds. His mental faculties were unscathed, and he slowly regained some movement and speech through therapy. Eventually, he was able to communicate, eat, operate a motorized wheelchair and write a book. He had another big dream, too. "Growing up, I fell in love with hiking, being outdoors and the beauty of nature," he says. That was taken away from him for 10 years, Kapen says, but very recently, a new set of wheels has allowed for his return. It's called the AdvenChair [which] recently enabled Kapen to visit Machu Picchu. The orange, "all-terrain" wheelchair is human-powered and designed to help people with mobility challenges to venture into the wild. Its wheels, tires, brakes and handlebars are all premium mountain bike parts, and the large tires and suspension system offer a comfortable ride. Thanks to a versatile system of pulleys, bars and straps, teams of one to five people can assist in navigating the AdvenChair over just about any landscape. "It's rejuvenating to be outside, especially as a person with a disability, because these resources are not exactly the most accessible," [Isaac] Shannon says. "So when there is a tool that allows a person to be able to experience life in the most average way possible, I think it's healing, and it's nice to be out in nature where you're not around people."
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From Hawaii to Bali and the ski-slopes of Perisher, 26-year-old Jimmy Antram has seen plenty of the world. But it has all been from the vantage point of his mother's back. Fulfilling a promise she made to herself as a 17-year-old first-time mum to give her disabled son the best life she possibly could, Niki Antram has spent years travelling the globe with Jimmy clinging to her shoulders. Jimmy was born with physical and mental disabilities, including blindness, and requires round the clock care from Ms Antram and his support workers. He has a wheelchair, but Ms Antram has never enjoyed using it. She's content to carry him while she's physically able and helps him walk short distances on his own. Incredible photographs taken around the globe show him clinging on as they hike through mountains and rainforests. 'Planning big holidays, I always make sure I have plenty of nappies, clothes, and even bed pads, sheets and pillowcases,' she [said]. Ms Antram plans a meticulous itinerary and calls ahead for every venue she wants to visit - whether it be a restaurant, hotel or daredevil adventure. 'Even if I know we will be okay I like to inform the companies to give them a heads up about us to make sure they understand and are okay with having us there,' she says. Sometimes, they can't accommodate. This is usually because of risks associated with Jimmy's condition or logistical difficulties. Ms Antram said the exception to this was in Hawaii, where 'everyone wanted [Jimmy] to join'.
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An autistic teenager has become an online sensation after a video demonstrating his unique technique as a barista - which involves plenty of dancing - went viral. Sam was filmed making a cup of coffee for a customer while working alongside his boss Chris at the Starbucks restaurant, believed to be in North America. The clip shows the teenager smiling and dancing while heating the milk and later pouring it into the cup of coffee, before adding whipped cream and sprinkles. Carly Fleischmann, who lives in Toronto, Canada, posted the video to YouTube and Facebook alongside a caption introducing Sam. Carly explained that when Sam was offered a position at Starbucks he told his parents that for the first time in his life he felt like he had real meaning. She added: 'Sam was diagnosed with autism and like some people with autism Sam has a movement disorder. Sam has a hard time keeping his body still. 'Sam never thought that he would be able to work behind the bar because of his sudden movements but his manager Chris believed in him and got Sam to channel his movements into dance.' The partnership was not an overnight success however and it has taken Sam and Chris many shifts and hours to get to the level demonstrated in the video. Sam is now known as the 'dancing barista' and Carly noted that if it was not for Chris believing in the ability of his employee then he would not have had the confidence to believe in himself.
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Two pedals, one leg - the bicycle and Emmanuel Ofosu Yeboah weren’t exactly made for each other. He got on one anyway, and it changed his life. Changed other people’s lives, too. Now the San Diegan wants to do it all again. Yeboah, 38, was born in Ghana without a shinbone in his right leg. The deformity set him up for life as an outcast. His mother believed he could be more than that. Her dream became his dream. After she died, he decided to honor her hopes for him by cycling one-legged across Ghana. He wanted to raise awareness for the plight of the disabled while setting an example for what was possible. He rode a mountain bike almost 400 miles in 10 days, clad in a T-shirt with “The Pozo” - disabled person - printed on the front. “Pozo! Pozo!” people yelled as he rode by, but they weren’t making fun of him. They were cheering. By the time he was done, he’d gone from curiosity to national hero. Government officials, their eyes opened, eventually passed legislation giving the disabled greater rights. In 2005, he was the subject of a documentary, “Emmanuel’s Gift,” narrated by Oprah Winfrey. And then the public’s attention moved on, as it always does, to other dreams, to other dreamers. Except Yeboah isn’t finished with his. He wants to build a school in Ghana for the disabled. So he’s formed a nonprofit organization, Emmanuel’s Dream. But he also knows what got him noticed in the first place. He’s getting back on the bike. The plan is to ride from San Diego to Oregon, 1,082 miles in 21 days.
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Before my freshman year of high school started ... my friend's car hit a guardrail with me inside. The railing amputated my leg instantly. Several years ago, more of my leg had to be amputated. Not only did this make it harder to wear a prosthetic, but it became a lot more expensive. In February of 2013, my life was forever changed when I attended the Executive Assistant Organization's Behind Every Leader event. During the conference, a sweet lady by the name of Alisson Frew dared to ask me why I did not wear a prosthetic. My short and simple answer was, "I don't have sixty thousand dollars. Do you?" The next morning I was in tears as I learned that Alisson had talked with Jeff Hoffman, founder of Priceline and mentor to GiveForward.com, along with a dozen other people, in order to help me get a prosthetic. From the first step, it was apparent to me just how much this would mean. A few days after I received the leg, I wrapped my son in my arms and experienced our first of many dances. This seemingly simple moment is forever ingrained into my heart. For the first time in my life, I was not only confident but I was empowered! I yearned to help those around me. In ... 2014, I started modelling. My dream is that one day a little girl will see me on a poster at her favorite clothing store and say, "Wow, she is beautiful, and she only has one leg. I could do that too someday, even though I have a disability." My dream is simple: to inspire every man, woman, and child into knowing and believing that they are beautiful just the way they are.
Note: Watch Marina's inspiring thank-you video to Behind Every Leader.
Tim Harris was born with Down syndrome and his father, Keith, admits that acceptance didn't come easily at first. But over the years, Keith's attitude shifted. "Tim is the second of four boys, and when he was growing up, we saw the challenges that his disability presented socially,” Keith [said]. “We started to ponder when he was young about his future and made the choice that we wanted to create a life for him that was as close to typical as possible.” Thanks to his parents' faith and support, Harris has not only accomplished the typical, but he's also made the world a little bit more extraordinary. Today, Harris is the proud owner of Tim's Place, a successful -- and unique -- restaurant in Albuquerque, N.M. Other than selling regular New Mexican fare, Tim's Place has a trademark special. It's called the Tim Hug -— a "calorie-free" and "guilt-free" treat that, according to the menu description, guarantees to "improve your lease on life." "I love giving all the customers a hug because I want them to feel comfortable and connected and being around friends,” Harris told Albuquerque The Magazine. Tim's Place, which calls itself the "world's friendliest restaurant" opened its doors in 2010 and since then, Tim has given out more than 19,000 hugs. He keeps track using a Hug Counter. Only 26, Harris -- a college graduate -- is also an accomplished Special Olympian, an excellent sailor and an experienced offshore fisherman. In high school, Harris was also elected homecoming king and Student Of The Year.
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When Rick Hoyt was 15, he communicated something to his father that changed both their lives. "Dad," the mute quadriplegic wrote in his computer after his father pushed him in a wheelchair in a five-kilometer race, "I felt like I wasn't handicapped." Rick, now 37, has had cerebral palsy since birth. But he has always been treated simply as one of the family, included by his now-divorced parents in almost everything brothers Rob and Russell did. "They told us to put Rick away, in an institution, (because) he's going to be nothing but a vegetable for the rest of his life," his father remembers. "We said, 'No, we're not going to do that. We're going to bring Rick home and bring him up like any other child,'" says Dick Hoyt, 59, a retired lieutenant colonel with the Air National Guard. "And this is what we have done." For more than 20 years, Dick has either towed, pushed or carried Rick in a string of athletic challenges including every Boston Marathon since 1981 and, most recently, last month's Ironman Triathlon World Championships in Hawaii. But mental determination and physical stamina tell only part of the Hoyt story. A message of independence and acceptance typed by Rick on his computer complete the picture: "When I am running, my disability seems to disappear. It is the only place where truly I feel as an equal. Due to all the positive feedback, I do not feel handicapped at all. Rather, I feel that I am the intelligent person that I am with no limits. I have a message for the world which is this: To take time to get to know people with disabilities for the individuals they are."
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John Bramblitt believes he could draw before he could walk. Art was also his way of coping with spending much of his childhood in the hospital. After experiencing his first seizure at age 2, Bramblitt was diagnosed with severe epilepsy. After each seizure, his vision would remain blurry for a while, but then it would clear up. What neither he nor his doctors realized was that his vision was decreasing each time. In his mid-20s, while attending college for the second time at the University of North Texas in 2001, he received the news that he would lose the rest of his vision. There was nothing doctors could do to stop it. He was completely blind by the time fall semester began. When he was alone, he felt like he was losing his mind. That's when he remembered the joy he used to gain from creating art. He began by trying to draw simple shapes, but would feel his pencil run off the paper. Bramblitt realized he needed to create a structure to follow. Fabric paint, which would create raised lines as it dried, became his new pencil, and he used oil paints to bring the paintings to life. He used [touch] to "see" what he wanted to paint and to distinguish between oil paints, because each color had a different viscosity and texture. Encouraged by the way it made him feel, he would paint for hours every day. Over the years, Bramblitt has connected with charities and started a series of workshops for artists with and without sight, young and old. He believes art should be something everyone can connect with. After all, art changed his life.
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