Inspiring: People with Disabilities Media ArticlesExcerpts of Key Inspiring: People with Disabilities Media Articles in Major Media
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Last Friday, 6-year-old Landon Johnson went to the RiverTown Crossings Mall in Grandville with his family. While there, the boy and his cousins took turns chatting with Santa. After telling the man in red he wanted a Wii, a toy dinosaur and a remote control car, Landon hopped off Santa’s lap to rejoin his family. But a few moments later, he raced back to Santa’s side: he’d forgotten to tell him something important. “He wanted to tell [Santa] that he has autism,” Landon’s mom, Naomi Johnson, said in a moving Facebook post about the encounter this week. Specifically, Landon shared his worry with Santa that his autism would land him on the “naughty list.” His mom explained ... that Landon is often told he’s “naughty” by people who mistake his autism [for] bad behavior. He’s been told by other people before, "You don’t need to be so naughty," or, "Why are you naughty?" Santa took the time to listen to Landon's worries, and held the boy's hands soothingly all the while. “Santa sat him next to him and took L's hands in his and started rubbing them, calming them down. Santa asked L if it bothered him, having Autism? L said yes, sometimes. Then Santa told him it shouldn't. It shouldn't bother him to be who he is,” Johnson wrote. Landon told Santa that he sometimes “gets in trouble at school and it's hard for people to understand that he has autism,” but that he's “not a naughty boy.” “You know I love you and the reindeer love you and it’s OK. You’re a good boy,” Santa told WOOD-TV.
Note: Explore a treasure trove of concise summaries of incredibly inspiring news articles which will inspire you to make a difference.
Most children want to dress up for Halloween, but for those confined to wheelchairs, it isn’t always that simple. Ryan Weimer understands that concept better than most. When his oldest son, Keaton, was 3 years old, he told his dad he wanted to be a pirate for Halloween. Instead of simply dressing him up, Weimer spent months building Keaton - who lives with muscular dystrophy - a pirate ship made of wood, tablecloth sails and specially-crafted cannons, all fitted to his wheelchair. Keaton was ecstatic - and his dad never forgot the feeling. "When you know that you have few memories to make with your kids, you want to make priceless ones," Weimer told NBC News, "and epic ones." His second son, Bryce, also lives with muscular dystrophy. Over the years, their wheelchair costumes have gotten more elaborate and attracted more attention. And this year, the Weimer family project became a hugely successful non-profit, called Magic Wheelchair. Volunteers from around the country donated their time, talents and resources to create dream costumes for eight lucky children — six from Weimer’s home state of Oregon and two from Georgia. "When we have challenges and trials and hard times, those are the things that define us," Weimer said. "It doesn’t' matter your circumstances, you can still make beautiful things ... and it's great to see other people get behind that."
Note: Don't miss this very touching video on Magic Wheelchairs.
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.
Note: Watch a great documentary on this most inspiring man. Explore a treasure trove of concise summaries of incredibly inspiring disabled persons news articles which will inspire you to make a difference.
Dan Nevins commands his yoga class with authority. For Nevins, teaching yoga is much more than a job. It actually saved his life. Eleven years ago, while serving in Iraq, an IED exploded under his Army vehicle. The blast destroyed both his legs. "I just remember having this revelation that I'm alive, I'm alive! That I better do something to keep it that way." Nevins spent 18 months at Walter Reed Medical Center. With the help of the Wounded Warrior Project, he learned to climb mountains and play golf. But two years ago, while recovering from another surgery, he was bedridden and started having flashbacks. "And those thoughts of the not-so-great experiences from combat just kept coming back. I didn't get to the point of suicide, but I finally understood in those 8 weeks at home and I knew that I needed help." A friend suggested yoga to Nevins. "I was like 'No. One, I'm a guy; Two, I'm an Army guy; Three, I don't own any spandex, and no.'" Despite his reservations, he finally relented and took the class. "I got into this Warrior One pose. I rooted down and I felt this real surge of energy from the earth up into my body like into my soul and I shot up like 'Oh my God, I get it,' like the earth was saying 'where have you been the last ten years.'" Last year, Nevins completed yoga instructor training. Now hundreds of people come to his classes. "I felt if he can do it without legs, what's my excuse," said one student. Nevins hopes to reach both veterans and non-veterans alike.
Note: Don't miss the pictures of this inspiring yoga practice available at the link above.
Kanya Sesser, 23, skateboards, models lingerie and surfs – and she does it all without lower limbs. Sesser, who was born without legs, was adopted from an orphanage in Thailand before moving to Portland, Oregon, with her new family. Now, she earns more than $1,000 a day working as a model. "I enjoy making money from it and I love showing people what beauty can look like," Sesser told the Daily News. "These images show my strength." The 23-year-old, who uses a skateboard instead of a wheelchair, began modeling for sports brands when she was 15. The Huffington Post UK reports that the Los Angeles-based model has reportedly posed for brands like Billabong, Rip Curl Girl and Nike. "I was mainly doing athletics shoots then as I got older I got into lingerie modeling," Sesser told the Daily News. "It's something fun and it shows my story – I'm different and that is sexy, I don't need legs to feel sexy." Now, the model hopes to compete in the 2018 Winter Paralympics in Pyeongchang, South Korea, as a mono-skier.
Note: Don't miss this inspiring seven-minute video of Kanya's courage and fascinating life.
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.
Note: Read another great piece on this inspiring woman.
John Bramblitt of Denton, Texas, lost his vision 13 years ago due to complications with epilepsy and plunged into a deep depression, feeling disconnected from the world around him. He found a new way to express his experience of the world around him in painting however. Bramblitt learned to distinguish between different coloured paints by feeling their textures with his fingers, taught himself how to paint using raised lines and harnessed haptic visualization, enabling him to "see" his subjects through touch. While many of his portraits are taken from events in his life he experienced while sighted, he has also produced life-like paintings of people he's never actually seen, including his wife and son. Art was always a big part of his life but took on a new importance following his blindness. "Art reshaped my life," he said. Whilst continuing to create new works, Bramblitt teaches art workshops focusing on adaptive techniques for young artists with disabilities, for which he has received three Presidential Service Awards. You can buy originals and prints of John's work here.
Note: Don't miss the incredibly inspiring one-minute video of this inspiring blind artist.
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.
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."
Note: Don't miss the most awesome video of Richie at the link above. For a treasure trove of great news articles which will inspire you to make a difference, click here.
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.
Note: For the CBS 60 Minutes piece on this child genius, click here. For a treasure trove of great news articles which will inspire you to make a difference, click here.
Jessica Cox was born without arms as a result of a rare birth defect. That has not stopped her from living her life to the fullest. In fact, Ms Cox has experienced and achieved more than most people do in a lifetime. She can drive a car, fly a plane and play piano - all with her feet. In 2012 she married Patrick, her former Taekwondo instructor (she has two black belts). They live in Tucson, Arizona. Ms Cox, 30, travels around the world as a motivational speaker, using her own life as an example of what one can achieve if one wants it enough. This month she visits Ethiopia to help promote disability rights.
Note: Don't miss the inspiring video on the BBC webpage. And for another incredibly inspiring man born without arms or feet, learn about Nick Vujicic at this link.
In 1978, 5-year-old Frank "Bopsy" Salazar was diagnosed with leukemia. A woman named Linda Pauling ... had lost her 7-year-old son, Chris, to leukemia that spring. But before Chris passed, the Arizona Department of Public Safety had fulfilled the little boy's dream of becoming a police officer. DPS officers Jim Eaves and Frank Shankwitz had met Chris with a patrol car and motorcycle and made him the only honorary Arizona Highway Patrol Officer in the department's history. The incredible effort inspired Pauling and Shankwitz to start the Make-A-Wish Foundation. "[Pauling] told me that instead of letting the kids just feel sorry for themselves, they wanted to grant wishes, to do something every kid would benefit from, to fulfill their dream while they're still a part of this world," Trujillo said. Shankwitz took over from there, and he went to visit Bopsy to find out more about the boy's dreams. After learning that he'd be granted a wish, the 7-year-old mulled it over. "I want to ride in a hot air balloon," he told Shankwitz. Then he thought about it some more. "No, I want to go to Disneyland." He paused again. "No, I want to be a fireman." But Shankwitz didn't make him pick. All of Bopsy's wishes would be granted. He got his balloon ride and his trip to Disneyland. Fireman Bob - whose real name is Bob Walp - did more than was asked of him to help the sick boy. "We didn't want to just give him a tour," Walp [recalled]. "We decided to give him a badge and a jacket. We let him use the hose. We took him in the truck."
Note: For more on this inspiring story, see this webpage.
When she was in high school, Lizzie Velasquez was dubbed "The World's Ugliest Woman" in an 8-second-long YouTube video. Born with a medical condition so rare that just two other people in the world are thought to have it, Velasquez has no adipose tissue and cannot create muscle, store energy, or gain weight. She has zero percent body fat and weighs just 60 pounds. In the comments on YouTube, viewers called her "it" and "monster" and encouraged her to kill herself. Instead, Velasquez set four goals: To become a motivational speaker, to publish a book, to graduate college, and to build a family and a career for herself. Now 23 years old, she's been a motivational speaker for seven years and has given more than 200 workshops on embracing uniqueness, dealing with bullies, and overcoming obstacles. She's a senior majoring in Communications at Texas State University in San Marcos, where she lives with her best friend. Her first book, Lizzie Beautiful, came out in 2010 and her second, Be Beautiful, Be You, was published earlier this month. She's even reclaimed YouTube, video blogging about everything from bullying to hair-styling tips to staying positive. Of course, the horrible comments left on that old YouTube video stung. "I'm human, and of course these things are going to hurt," she said. "Their judgments of me isn't who I am, and I'm not going to let these things define me. I didn't sink down to their level," she said in a follow-up video on YouTube last year. "Instead, I got my revenge through my accomplishments and determination. In the battle between the 'World's Ugliest Woman' video vs. me, I think I won."
Note: Though looking at this woman can be disturbing for some, consider that you can see beneath the surface to the beauty within. Watch Lizzie share some of her wisdom in a popular TEDx Talk at this link.
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.
Note: Don't miss the awesome three-minute video of Tim and his restaurant! Explore a treasure trove of concise summaries of incredibly inspiring news articles which will inspire you to make a difference.
Arthur Boorman was a disabled veteran of the Gulf War for 15 years, and was told by his doctors that he would never be able to walk on his own, ever again. He stumbled upon an article about Diamond Dallas Page doing Yoga and decided to give it a try -- he couldn't do traditional, higher impact exercise, so he tried DDP YOGA and sent an email to Dallas telling him his story. Dallas was so moved by his story, he began emailing and speaking on the phone with Arthur throughout his journey - he encouraged Arthur to keep going and to believe that anything was possible. Even though doctors told him walking would never happen, Arthur was persistent. He fell many times, but kept going. Arthur was getting stronger rapidly, and he was losing weight at an incredible rate! Because of DDP's specialized workout, he gained tremendous balance and flexibility -- which gave him hope that maybe someday, he'd be able to walk again. His story is proof, that we cannot place limits on what we are capable of doing, because we often do not know our own potential. Neither Arthur, nor Dallas knew what he would go on to accomplish, but this video speaks for itself. In less than a year, Arthur completely transformed his life. If only he had known what he was capable of, 15 years earlier.
Note: For an awesome, five-minute video on this inspiring transformation, click here. For a treasure trove of great news articles which will inspire you to make a difference, click here.
Think of it sort as an updated take on "Hoop Dreams," except that its basketball-playing dreamers use wheelchairs. And they live in Afghanistan, not the Windy City. Jess Markt, originally from the Portland, Ore. area, is ... at the center of "The League of Afghanistan," a new documentary film currently in development. In 2009, Markt, whose spinal cord was injured in a car accident at the age of 19 and [who] relies on a wheelchair to get around, traveled to northwest Afghanistan to coach a wheelchair basketball team hoping to create a nationwide league. When Aaron Cooley, a Los Angeles-based producer with Joel Schumacher's production company, caught wind of Markt's experience, he saw the seeds of a great film. Today, the documentary, which aims to tell the story of Markt's efforts to bring basketball to disabled men and women [throughout Afghanistan], is in its early stages of filming. From Jess' perspective, he is the outsider American who comes into a legitimately ... hostile situation. For the local players, we're looking at how the introduction of this game can help rebuild the hope and the purpose that is in their own lives, which were shattered by their own injuries.
Note: Don't miss the inspiring video on this beautiful story. Explore a treasure trove of concise summaries of incredibly inspiring news articles which will inspire you to make a difference.
Amber Miller accomplished two monumental feats this weekend. Days from her due date, the 27-year-old joined 45,000 other runners to participate in Sunday's Bank of America Chicago Marathon and then gave birth to a baby girl named June hours later. Miller, an avid runner, said she signed up for the 26.2-mile race before finding out she was pregnant. She said she never expected to finish the race. "I was having a conversation with my parents and said, 'You know what? I have no plans of actually finishing,'" she told reporters at Central DuPage Hospital this morning. "I was planning on running half, skipping to the end, then walking across the finish line." But Miller and her husband started running, and just kept going. They ran part of the race and walked the second half as her contractions started. It took the couple 6.5 hours to finish. She said she grabbed something to eat and the two headed to the hospital. "It was very interesting hearing people's reaction," Miller said about crowds watching an extremely pregnant woman among the runners. "I've been running up to this point anyway, so I'm used to it." At 7 pounds, 13 ounces, baby June entered the world at 10:29 p.m. Sunday, just hours after her parents crossed the finish line.
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.
Carly Fleischmann has severe autism and is unable to speak a word. But ... this 13-year-old has made a remarkable breakthrough. Two years ago, working with pictures and symbols on a computer keyboard, she started typing and spelling out words. The computer became her voice. "All of a sudden these words started to pour out of her, and it was an exciting moment because we didn't realize she had all these words," said speech pathologist Barbara Nash. Then Carly began opening up, describing what it was like to have autism. Carly writes about her frustrations with her siblings, how she understands their jokes and asks when can she go on a date. "We were stunned," Carly's father Arthur Fleischmann said. "We realized inside was an articulate, intelligent, emotive person that we had never met. This ... opened up a whole new way of looking at her." This is what Carly wants people to know about autism. "It is hard to be autistic because no one understands me. People look at me and assume I am dumb because I can't talk or I act differently than them. I think people get scared with things that look or seem different than them." Carly had another message for people who don't understand autism. "Autism is hard because you want to act one way, but you can't always do that. It's sad that sometimes people don't know that sometimes I can't stop myself and they get mad at me. If I could tell people one thing about autism it would be that I don't want to be this way. But I am, so don't be mad. Be understanding."
Note: Read an excellent follow-up article in which Carly answers readers questions about autism. For more, see this webpage.
When I met 18-year old Patrick Henry Hughes, I knew he was musically talented. I had been told so, had read that he was very able for someone his age and who had been blind and crippled since birth. Patrick's eyes are not functional; his body and legs are stunted. He is in a wheelchair. When we first shook hands, his fingers seemed entirely too thick to be nimble. So when he offered to play the piano for me and his father rolled his wheelchair up to the baby grand, I confess that I thought to myself, "Well, this will be sweet. He has overcome so much. How nice that he can play piano." But then Patrick put his hands to the keyboard, and his fingers began to race across it -- the entire span of it, his fingers moving up and back and over and across the keys so quickly and intricately that my fully-functional eyesight couldn't keep up with them. I was stunned. The music his hands drew from that piano was so lovely and lyrical and haunting, so rich and complex and beyond anything I had imagined he would play that there was nothing I could say. All I could do was listen. "God made me blind and didn't give me the ability to walk. I mean, big deal." Patrick said, smiling. "He gave me the talent to play piano and trumpet and all that good stuff." This is Patrick's philosophy in life, and he wants people to know it. "I'm the kind of person that's always going to fight till I win," he said. Patrick also attends the University of Louisville and plays trumpet in the marching band. The band director suggested it, and Patrick and his father, Patrick John Hughes, who have faced tougher challenges together, decided "Why not?" "Don't tell us we can't do something," Patrick's father added, with a chuckle. He looks at Patrick with a mixture of love and loyalty and admiration, something not always seen in the eyes of a father when he gazes at his son. "I've told him before. He's my hero."
Note: For amazingly inspiring video clips of this unusual young musician on both Oprah and ESPN, click here and here.
Important Note: Explore our full index to key excerpts of revealing major media news articles on several dozen engaging topics. And don't miss amazing excerpts from 20 of the most revealing news articles ever published.