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Glenn Cunningham, a former world-record holder in the mile run who in 1979 was named the greatest track performer in the history of Madison Square Garden, died yesterday. He was 78 years old. That Mr. Cunningham could win 21 of 31 mile races on the indoor track at the Garden during his prime in the 1930's was impressive. More significantly, he did it after suffering life-threatening burns on both legs as a 7-year-old when a stove in a school classroom in Everetts, Kan., exploded, killing his older brother Floyd. After being told there was a strong possibility he would never walk again, he spent seven months in bed, and then received daily massages from his mother, who kneaded his damaged muscles and sped his way to walking, and then running. In high school, he played baseball and football and boxed and wrestled. At 13, he entered his first high school mile race and won easily. Using running as therapy for the burn injuries, he found that middle distances suited him. At a sophomore at the University of Kansas, Mr. Cunningham set an American record for the mile with a time of 4 minutes 11.1 seconds. He was selected as a member of the United States team for the 1932 Olympic Games in Los Angeles, and finished fourth in the 1,500-meter run. In 1933 he won the Sullivan Award as the nation's top amateur athlete. In his competitions at Madison Square Garden, Mr. Cunningham set six world records in the mile and the 1,500 meters and another at 1,000 yards.
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Judith Heumann, who had polio as a baby and uses a wheelchair, started her activism early. After graduating from college, she applied for a teaching license but was rejected by the New York City board of education, which called her a fire hazard. Heumann sued for discrimination and won in a landmark case, becoming the first wheelchair user to teach in the city’s schools. That victory put Heumann in the spotlight. She founded her own disability-rights group in 1970 and became an advocate for the independent-living movement. She successfully pushed Richard Nixon to sign the first federal civil rights legislation for disabled people. But when regulations for the Rehabilitation Act of 1973 were stalled, Heumann helped organize more than 100 disabled activists to stage a sit-in, named for the law’s section on disabilities, at a San Francisco federal building in 1977. The 504 Sit-in, which lasted 28 days, challenged the perception of people with disabilities as helpless or objects of pity. In Heumann’s words: “We demonstrated to the entire nation that disabled people could take control over our own lives and take leadership in the struggle for equality.” The 504 Sit-in accomplished its goal, and those protections laid the groundwork for the Americans with Disabilities Act. Heumann, who served in the Education and State departments of the Clinton and Obama administrations, has continued to advance the rights of disabled people around the world.
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Completing two marathons on crutches while partially paralyzed is a testament to the resilience of the human spirit. Three years after a spinal cord injury that left her without full mobility of her lower body, Hannah Gavios completed her second New York City Marathon - crossing the finish line on crutches in just over 11 hours, 18 minutes faster than last year. The sun had gone down by the time she reached the end of the 26.2-mile course. But achieving that milestone yet another time was a powerful reminder of everything she had overcome. In 2016, Gavios took a vacation to Thailand from her job teaching English in Vietnam. On her way back to her hotel one night, she feared she had gotten lost and asked for directions. But the person who had been guiding her ended up leading her to a dark, wooded area and attacked her, Gavios told CNN. While running away from her attacker, she fell off a cliff, tumbling 150 feet. The fall left her with a spinal cord injury that has affected muscles in her lower body. But it hasn't stopped her from living her life to the fullest. "I always knew I was a strong person," the 26-year-old Queens, New York, resident said. "But I didn't know I was that strong. I also didn't realize how much of a fighter I was." Then she learned about Amanda Sullivan, who had been completing marathons on crutches after an auto accident left her disabled. If someone with a similar condition could finish a marathon, Gavios thought to herself, then she could, too.
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A Paraguayan father of two with no arms or legs found the strength and determination to raise both his girls, despite his limitations, when their mother abandoned them. Pablo Acuña was born with a limb deformity, causing his arms and legs to not grow properly. Yet he's a happy, grateful man who lives in the city of Son Pedro del Parana, Paraguay. At 63 years old, he's a proud father of two daughters in their twenties, whom he has raised since they were babies with the help of his mother, Ignacia del Valle. Although Pablo has suffered from his condition since his birth, he said it has never affected him. Apart from not being able to attend high school and having his parents take care of him, he had a pretty normal childhood. His youngest daughter, Elida, 26, sings his praises for providing a "very nice" childhood despite him not having arms and legs. "I was raised by my dad and grandmother," Elida said. "My dad is incredible. He is a very wonderful person, he is always seen with a smile; never have I seen him depressed." Since Pablo cannot walk, he has used a wooden wheelbarrow as a sitting and sleeping platform for decades. He is known locally as "El Hombre Carretilla," or "The Wheelbarrow Man." According to Elida, Pablo's greatest wish is to own his home. Elida [said] that her family, who "lives for rent," is desperately saving to this end. Since her grandmother turned 93, Elida has returned to the family home ... to help take care of her father.
Note: After reading this article, one man spearheaded a campaign which enabled this amazing dad to buy his own home. Explore more stories like this in our inspiring disabled persons articles archive.
When Trinity Jagdeo’s best friend was diagnosed with Spinal Muscular Atrophy Type 2, a rare and serious degenerative disease, Trinity wished her friend had a hero she could relate to, someone to inspire her. She couldn’t find one. So she created one. “Seeing what my best friend was going through, I wanted to do more for others like her.” In 2014, her friend Alexus Dick was hospitalized for six months. “I took note of how drained she was. She had nobody to look up to while she was going through that battle.” Trinity’s first instinct was to reach out to Disney, asking for more characters with disabilities or special needs. “I wrote them letters, made Youtube videos. I didn’t receive a response, so I decided to create my own non-profit, and I began writing and illustrating my own books that featured local special-needs kids.” Alexus was thrilled when she saw Trinity’s comic books starring heroes with disabilities. “I was excited when I realized what she was doing. She was right, there were no characters with disabilities.” Trinity ... found an inexpensive drawing pad that connected to her computer, and she began to use Amazon’s publishing tools. “I put the entire thing together, and they’d print it out for me.” This was when Trinity was 17. Trinity has written and illustrated three books so far. “I love all of the kids I write about, and they all inspire me. I actually illustrated Alexus’s brother, who also has spinal muscular atrophy.” His book is titled “Zappy Zane.” Her other two titles are “Alice the Ace” and “The We Can Squad Saves the Day.”
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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.
In most people, speech and language live in the brain's left hemisphere. Mora Leeb is not most people. When she was 9 months old, surgeons removed the left side of her brain. Yet at 15, Mora plays soccer, tells jokes, gets her nails done, and, in many ways, lives the life of a typical teenager. "I can be described as a glass-half-full girl," she says, pronouncing each word carefully and without inflection. Her slow, cadence-free speech is one sign of a brain that has had to reorganize its language circuits. Yet to a remarkable degree, Mora's right hemisphere has taken on jobs usually done on the left side. It's an extreme version of brain plasticity, the process that allows a brain to modify its connections to adapt to new circumstances. People like Mora represent the upper bounds of human brain plasticity because their brains were radically altered very early in life – a period when the wiring is still a work in progress. During an interview with Mora, both her abilities and deficits were apparent. So was her outgoing personality and curiosity about the world. Mora began by telling me a joke: "How do you make a hot dog stand?" she asks. "You take away its chair." What scientists still want to know is precisely what allowed Mora's brain to rewire so extensively. One thing is clear: Understanding the basis of this sort of extreme plasticity, they say, could help millions of people whose brains are still trying to recover from a stroke, tumor, or traumatic injury. And Mora is helping scientists deepen their understanding, simply by being herself.
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Thomas Panek has completed 20 marathons, however, he made history on Sunday at the New York City Half Marathon. While visually impaired runners usually use human guides, Mr Panek became the first person to complete the race supported by guide dogs. A trio of Labradors - Westley, Waffle and Gus - each accompanied him for a third of the race. The team finished in two hours and 21 minutes. Mr Panek, who lost his sight in his early 20s, told CNN that while he appreciated the support of human volunteers, he missed the feeling of independence. "It never made sense to me to walk out the door and leave my guide dog behind when I love to run and they love to run," he said. "It was just a matter of bucking conventional wisdom and saying why not. In 2015, Mr Panek established the Running Guides programme which trains dogs to support runners. "The bond is really important. You can't just pick up the harness and go for a run with these dogs," Mr Panek told CNN. "You're training with a team no matter what kind of athlete you are, and you want to spend time together in that training camp." Each dog wears a special harness and set of running boots, to protect their paws. Before the race, Mr Panek told Time magazine that guide dogs give visually impaired people the freedom to "do whatever it is a sighted person does, and sometimes, even run a little faster than them".
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Reaching the summit of Mount Everest is a triumph for any climber, but for Erik Weihenmayer, the accomplishment is even more impressive. That’s because he is blind. Born with a rare eye disease, Mr. Weihenmayer lost his sight at age 13 and later discovered a sense of freedom through climbing. Over the years, the 50-year-old has reached the highest peaks on seven continents and also kayaked the Colorado River through the Grand Canyon. A former schoolteacher, Mr. Weihenmayer co-founded No Barriers, a nonprofit organization that teaches outdoor skills to those with physical challenges. "Growing up in Connecticut, my Dad would drive me three hours to Massachusetts once a month to this adventure program for the blind, [said Mr. Weihenmayer]. "They took us to New Hampshire and we rock climbed on these beautiful granite rock faces. It was very tactile. That’s what I really loved about it. You can feel all these little knobs and cracks and fissures and little dishes in the rock. So you’re problem-solving with your hands and feet as your eyes. You had to put your body in all these cool, acrobatic positions to get yourself from point A to point B and you’re trying to solve this puzzle that’s embedded in the rock. I loved the great adventure. I got to the top and I could hear the valley below me. I could hear the wind blowing through the trees. And I thought this is so stunning. This is what I want out of my life."
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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.
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When Charles King went blind at 39, he gave up — on life, on his pregnant girlfriend, and on himself. “I said ‘OK God, that’s it. I quit.’ I literally quit and just went out on the streets and joined the homeless,” he said. “I hoped that because I was blind, someone on the streets would kill me.” But going blind and becoming homeless wasn’t the toughest battle King would have to face. In 2000, after he got clean and was reunited with his family, King’s 14-year-old daughter died. Five years after that, he was diagnosed with cancer. And yet, somehow he’s lifted himself up — both mentally and physically. Today, the 69-year-old Philadelphian is one of the oldest blind powerlifters in the world, having finished first in his weight and age class last month at the United States Association of Blind Athletes National Powerlifting Championships in Colorado Springs, Colo., with a 248-pound squat, a 236-pound bench press, and a 341-pound dead lift. Now, King is inspiring other blind senior citizens. These days, when King feels the depression kicking in, he goes to the gym. Recently ... a student approached and asked if he could join him. After their workout was over, the young man confessed that he’d seen King around campus before but for some reason, was moved to approach him that day. “He says, ‘Mr. Charles, I thank God for meeting you today because I was ready to give up on my classes and goals because it’s too hard, but after watching you, I’m regenerated,’” King recalled. “I said, ‘Son, God blessed both of us today.’ ”
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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.
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Chris Nikic became the first athlete with Down syndrome to complete the Ironman World Championship when he crossed the finish line during Thursday's event in Kailua-Kona, Hawaii. The Ironman involves three events: a 2.4-mile swim, a 112-mile bike ride, and a 26.2-mile run. Nikic finished in 16 hours, 31 minutes and 27 seconds. He completed the swim in one hour, 42 minutes, the bike ride in eight hours, five minutes and the run in six hours and 29 minutes, placing 2,265th out of 2,314 athletes that competed that day. Nikic, who celebrated his 23rd birthday after crossing the finish line with his volunteer guide, accomplished the feat during Down syndrome awareness month. Nikic's perseverance has won him many admirers and his dedication won him the 2021 Jimmy V Award for Perseverance at the ESPYs after he became the first person with Down syndrome to finish an Ironman triathlon after completing the Florida Ironman in November 2020. In a video, Nikic explained his motivation in competing in the grueling events. "I rarely saw anyone who looks like me in mainstream sports. And now, we're changing that," Nikic said. "Running changed my life, but now I want everyone like me to see it's possible for them, too."
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At only 10 years old, [Devan Watkins] went from being an energetic sports-oriented kid to one with paraplegia navigating a new way of life from a wheelchair. It wasn’t long before he learned about adaptive sports from his physical therapist who suggested he try wheelchair basketball. Devan attended his first practice in his regular wheelchair, and for the first time since his surgery, he realized he was not alone with his new disability. Trooper Johnson coached the league along with Team USA’s Paralympic wheelchair basketball superstar, Jorge Sanchez. Jorge mentored Watkins on his new journey and introduced the Watkins family to the Challenged Athletes Foundation (CAF), the world leader in helping people with physical challenges lead active, healthy lifestyles. CAF has given over 26,000 grants to individuals with permanent physical disabilities. As a growing 12-year-old, Devan soon found it harder to fit in the borrowed basketball wheelchairs the league offered. His mom applied for a CAF grant. He was invited to attend the Golden State Warriors practice facility for a special surprise. What he didn’t know was that Jorge Sanchez and CAF had been working behind the scenes with the Warriors to orchestrate a surprise. Devan was escorted into Chase Stadium and ... Coach Steve Kerr rolled out a brand new customized PER4MAX® basketball wheelchair on behalf of CAF. “I was very shocked. This piece of equipment and all the tips from Jorge Sanchez are so helpful,” Devan said after shooting a few hoops.
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The 2,190-mile long Appalachian Trail is daunting even to those who have no trouble walking. That hasn't stopped Stacey Kozel. Her paralyzed body hasn't stopped her, either. The 41-year-old ... was always active until lupus stole her muscles and strength. Since her diagnosis at 19, she ... had always managed to get back on her feet - until a flare-up in March 2014. "I walked into a hospital, came out in a wheelchair," recalled Stacey Kozel. Although Kozel was able to walk stiffly with an old pair of braces, they wouldn't help her walk comfortably enough to embrace the outdoors. The chance finally came when she came across the Ottobock C-Brace. The brace functions essentially as the muscles and bones of a leg. The price tag for the technology was steep: $75,000 each. Kozel's doctors and therapists knew that getting these braces covered by insurance would be an uphill climb. When her claim was finally approved after 12 months, she was "in shock." Three days after Kozel got her braces, Joey Pollak, Kozel's orthopedist, got a call saying Kozel was in a 5K race. "To say Stacey is an overachiever is an understatement," said Pollak. What Pollak did not know was an idea forming in Kozel's head. She wanted to show insurance companies how useful the braces can be for those who have lost their mobility. She set her mind on the Appalachian Trail, just two months after she received her braces. Now, with support from her orthopedist, her mother and strangers along the way, she is slowly approaching her destination.
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One man is on a mission to become the first double amputee to sail around the world alone. Dustin Reynolds is currently docked at Bristol Marine. He refers to himself on social media as "The Single Handed Sailor," as he lost an arm and a leg in a tragic car crash in 2008. "I was trying to decide what to do next with my life," he said, "Randomly I was on the internet and I found a list of people who had set the record for sailing around the world alone. I was like, â€Well there's no double amputee on the list, I guess I'll just do that.'" And that's exactly what he's been doing for the past six years. He began his journey in June of 2014. Reynolds essentially taught himself how to sail through reading and watching videos on the internet. He mastered it single-handedly, literally, through trial and error. "Using one hand takes longer. You have to practice and sometimes use profanities. If that doesn't work you have to think of something else to do," said Reynolds. He started his circumnavigation from his home in Hawaii and so far has sailed through the South Pacific, Southeast Asia, and Africa. "It's a really meditative thing – spending that much time by yourself," he said. Reynolds actually went bankrupt trying to pay all his medical bills after the crash in 2008, so his entire adventure is funded through crowdsourcing. In each new place he stops, he tries immersing himself in the culture there, as well as shares his own story. His ultimate goal is to [complete] his circumnavigation in November of 2021.
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She didn't say a word – and that only made her message resonate more powerfully. Valedictorian Elizabeth Bonker recently delivered the commencement speech at Rollins College in Florida, urging her classmates to serve others and embrace the power of sharing. Bonker, who is affected by nonspeaking autism, hasn't spoken since she was 15 months old. But thanks to an accepting attitude from her peers and teachers and help from technology, she has overcome many challenges and graduated at the top of her class at the Orlando-area school. Bonker used text-to-speech software to deliver the commencement address – an honor for which she was chosen by her fellow valedictorians. "I have typed this speech with one finger with a communication partner holding a keyboard," she said. "I am one of the lucky few nonspeaking autistics who have been taught to type. That one critical intervention unlocked my mind from its silent cage, enabling me to communicate and to be educated like my hero Helen Keller." In her speech, Bonker also evoked another hero: Fred Rogers, the Florida college's most famous alumnus. Last year, the school unveiled a statue of the man widely known as Mister Rogers. And it has long embraced his lessons. "When he died, a handwritten note was found in his wallet," Bonker said. "It said, 'Life is for service.'" She urged her classmates to rip off a piece of paper from their program, write those words down, and tuck the message away in a safe place.
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When Jonathan Tiong was an infant, a neurologist told his parents that he wouldn't live past the age of two. He was diagnosed with type two spinal muscular atrophy, a rare genetic condition that causes muscles to become weak and break down. It is also a progressive disease, meaning he has become ... weaker with time. But in October, the same day he turned 24 years old, he was crowned valedictorian for the National University of Singapore's (NUS) Class of 2021, with the equivalent of a first class honours. He has also landed a prestigious job at sovereign wealth fund GIC, where he currently works full-time as an editorial writer. Speaking to CNA in his home, Mr Tiong candidly described himself as "a very plain and average student" throughout university. In his spare time, he immerses himself in the online game Runescape and watches Twitch streams. He regularly pens columns and blogposts, owing to a love of writing sparked in recent years. "I didn't think I'd be valedictorian for the simple reason that I was not a typical valedictorian. I didn't lead a (co-curricular activity), I wasn't the captain of some sports team, that kind of thing. "I studied a lot, got good grades, but so did a lot of other people. So I didn't really feel outstanding." This is despite the extra challenges he had to grapple with throughout school – namely, fatigue and accessibility in a world mostly built for able-bodied people. Poking fun at NUS' infamously hilly terrain, Mr Tiong joked that the university is also known as the "National University of Stairs".
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For eight-year-old Toby, who is deaf, watching films or TV on streaming platforms can sometimes be a bit pointless - because so many of them don't have sign language versions. "We have captions but they don't really do anything for him because it goes quite fast. He would just watch and not get much from it," his dad Jarod Mills [said]. But now, Toby has some help thanks to an app developed by a 17-year-old A-level student. Mariella Satow, who has dual UK-US citizenship, lives in the UK but has been stuck in New York since summer 2020 because of Covid travel restrictions. In that do-something-new phase of lockdown, Mariella created a signing app called SignUp. She got the idea when she was teaching herself American Sign Language (ASL) - one of hundreds of sign languages used across the world. Mariella wanted to watch TV shows to help her learn, so was disappointed to discover how few had signed versions. It's taken a year for Mariella to develop the technology, with lots of help from ASL teachers and the deaf community. The app is available in the US as a Google Chrome extension - with an interpreter appearing in a box once the film starts playing. It only works on Disney Plus films at the moment, because that's where Mariella thought she could help the most children. Jarod, who works in Kentucky at a school for deaf children, says it was "exciting" watching Toby use Mariella's invention. "The app creates a level playing field," he says. "Kids are getting that understanding and information like any hearing child does."
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City council member ÉlĂ©onore Laloux barely fills out her desk chair but her persona and vision outsize any of the Arras giants. "I'm a very committed and dynamic person, and I like to be out working with people," says Ms. Laloux. She's become a household name in Arras and regularly receives congratulations from locals for her dedication to her work. Ms. Laloux is the first and so far only person with Down syndrome to be elected to public office in France. Last year, she was put in charge of inclusion and happiness in Arras, bringing an effervescent energy to city decisions. Alongside Mayor FrĂ©dĂ©ric Leturque, Ms. Laloux has utilized her lived experience and innovative ideas to make sure inclusion and accessibility are a part of every city initiative – from education to transportation to tourism. Ms. Laloux is not just helping the city rethink what inclusion means, but also changing minds about what it's like to live with a disability as well as what those with cognitive disabilities are capable of. "Inclusion isn't something that we just think about; it's not a generous act. It's our duty," says Mr. Leturque, who put forward Ms. Laloux as a candidate last year. "ElĂ©onore has helped the entire town progress in terms of how we see disability." France doesn't take census-type statistics on people with disabilities, but Ms. Laloux is one of the few French people with a visible disability to hold a political position here. Her mere presence has transformed Arras into a model of accessibility and inclusion, and can have an impact on towns across France.
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