Inspiring Disabled Persons News StoriesExcerpts of Key Inspiring Disabled Persons News Stories in Major Media
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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 Ă‰lĂ©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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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, '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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By his own assessment, Dick Hoyt wasn't in racing shape the first time his teenage son Rick, a quadriplegic with cerebral palsy, asked if they could participate in a 5-mile fund-raising race – father pushing son in a wheelchair. "I said, 'Yeah, let's go down there and try it.' I had no idea what would happen, and nobody else did, either," Mr. Hoyt later recalled. "Most people expected us to go down to the corner and come back, but we ended up doing the whole thing." From those first racing steps, the two became legends in running circles and inspirational worldwide as they participated in more than 1,000 competitions, including dozens of marathons and multiple triathlons. Mr. Hoyt ... was 80 when he died of heart failure Wednesday. Though Mr. Hoyt and Rick posted a best time of 2:40:47 in the Marine Corps Marathon – a pace many marathoners will never touch running alone – the teaming of father and son was, for both, more important than all else. "When we're out there," Mr. Hoyt told the Globe in 1990, "there's nothing I feel I can't do with Rick." "Dick started this whole movement of duos, and Team Hoyt inspired thousands of people around the world," said longtime Boston Marathon race director Dave McGillivray. "He helped open the door to people believing in themselves, and the walls of intimidation crumbled." Most runners would be too intimidated to even try what Mr. Hoyt did over and over again – push a wheelchair carrying a boy, who became a grown man, up and down hills for 26.2 miles.
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Jordan Reeves is just an ordinary 14-year-old girl who has inspired millions of people with her extraordinary "superpower." The young inventor from Columbia, Missouri was born with a left arm that stopped developing beyond the elbow. Although some people would look at her under-developed limb as just a disability, Jordan used her condition to launch her superhero alter ego. When she was 10 years old, Jordan attended a STEM workshop that encouraged kids with disabilities to think creatively about their condition - so with a 3D-printer at her disposal, she designed her own prosthetic arm that could shoot glitter from the tip. Jordan's invention was so dazzlingly successful, she went on to talk about her horn-shaped "Project Unicorn" prosthetic design on the TEDx stage, Shark Tank, and even The Rachel Ray Show. With each appearance, she hoped that Project Unicorn would encourage other kids to view disabilities as gifts rather than hindrances. As Project Unicorn gained more traction, Jordan and her mother turned their labor of love into the Born Just Right nonprofit so they could continue advocating for inclusivity. In addition to publishing a book about her experiences in 2019, Jordan and her prosthetic were featured on Episode One of Marvel's Superhero Project - and earlier this week, she was featured on a new LEGO documentary miniseries that interviews young change-makers from across North America. More than 430 children from 30 different countries contributed.
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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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When Encinitas, Calif., teenager Ariella Pacheco was a little girl, her parents let her choose from a catalog the American Girl doll that most appealed to her. She picked the one with the hair color and style that matched her own. But what about children with rare medical conditions who don’t look like anyone else, including the mass-produced dolls on store shelves? Pacheco wanted to give these children the same gift she got as a child. So, over the past several months, she has designed and sewn cloth dolls for four local youth. “I really value the beauty in the little things,” Pacheco said. “Each of these kids are so unique, so special. I hope through these dolls they can see themselves in a new light and really embrace their beauty.” She ... designed her own patterns and figured out how to re-create the children’s differences. It was important to her that the children recognize themselves in the dolls but that their differences not be the most noticeable feature. “I hope they’re really excited with them,” Pacheco said. “The whole time I was trying to put as much love into it as I could and hoped they represented each child faithfully.” The inspiration for the four dolls are Felix, a 6-year-old boy with a large scar on his head from surgery for a skull fracture; Andrea, a 2-year-old with a port-wine stain birthmark on her face; Valeria, a toddler with Apert syndrome, which causes skull deformities, misshapen eyes and fused fingers; and Zulema Gillett, [who has] Goldenhar syndrome, which caused her to be born with a cleft lip, misaligned jaw, and only one ear.
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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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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.”
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.
There is something different, and a little special, about Universo Santi, a restaurant in the southern Spanish city of Jerez. “People don’t come here because the staff are disabled but because it’s the best restaurant in the area. Whatever reason they came for, the talking is about the food,” says Antonio Vila. Vila is the president of the Fundación Universo Accesible, a not-for-profit organisation dedicated to helping people with disabilities join the mainstream workforce. He has also been the driving force behind Universo Santi, the haute cuisine restaurant whose 20 employees all have some form of disability. “I always wanted to show what people with disabilities, given the right training, were capable of,” says Vila. “I feel really lucky to be part of this,” says Gloria Bazán, head of human resources, who has cerebral palsy. “It’s difficult to work when society just sees you as someone with a handicap. This has given me the opportunity to be independent and to participate like any other human being.” Alejandro Giménez, 23, has Down’s syndrome and is a commis chef. “It’s given me the chance to become independent doing something I’ve loved since I was a kid,” says Giménez, who lived with his mother until he was recruited. “Working here has transformed my life. So many things I used to ask my mother to do, I do myself. I didn’t even know how to take a train by myself because I’d just miss my stop.” Since it opened in October 2017, Universo Santi continues to win plaudits for its cuisine.
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.
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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[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.”
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.”
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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19-year-old Gabe Adams was born with Hanhart syndrome, a rare medical condition characterised by underdeveloped limbs, mouth and jaw. In Gabe’s case, none of his limbs grew at all. At school Gabe tried out for the dance team as a way of making friends – discovering he could use his limbless body to his advantage in the art of break dancing. After graduating from high school he has continued to prove his independence, moving out of the family home and embarking on a career as a motivational speaker. From a young age Gabe started using a wheelchair but his parents were determined that their son would be as independent as possible. At school Gabe would wedge a pencil or pen between his shoulder and cheek to write in class. ‘The day of the dance tryouts they called us all in a line and they said, “okay dancer remember to full out extensions and point your toes”. What am I gonna point? My nose!? ‘I am just standing there in front of the judges and then I see girls do the spins and I am like, “I can do that”, so I do the spins. ‘The next day at school and I hear two girls talking behind me and they say: “They are only gonna put him on the stage because he is handicapped’”and that crushed me. ‘I ran to the dance coach and I said “please do not put me on the team because you feel sorry for me”, and she said: “I would not put you or anybody else on the team because I felt sorry for them, you get a spot on this team because you deserved it”. ‘And that was just a huge opening moment for me.’
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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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Wilma Rudolph outran poverty, polio, scarlet fever and the limits placed on black women by societal convention to win three gold medals in sprint events at the 1960 Olympics in Rome. By the time brain cancer caught Rudolph, leading to her death Saturday at age 54, she had achieved a stature that made her legend and her sport greater in the long run. The 20th of 22 children of a porter and a cleaning lady, Rudolph lost the use of her left leg after contracting polio and scarlet fever at age 4. Doctors told her parents she never would walk again without braces, but she refused to accept that prognosis and began to walk unassisted at age 9. It wasn't long before she was outrunning all the girls and boys in her neighborhood. At 16, already under the tutelage of Tennessee State University coach Ed Temple, Rudolph won a bronze medal on the 4 x 100-meter relay at the 1956 Olympics in Melbourne, Australia. Four years later, when she was the mother of a 2-year-old, Rudolph won the three golds despite running all three events with a sprained ankle. After being voted Associated Press female athlete of the year in 1960 and 1961 and the Sullivan Award as the nation's top amateur athlete in 1961, Rudolph retired at 21, a decision that reflects an era in which lack of financial incentives kept most Olympic careers short. She turned to a variety of humanitarian projects, including goodwill ambassador to West Africa, coaching at DePauw University and working for underprivileged children through the Wilma Rudolph Foundation.
Note: The remarkable woman once commented, "My doctors told me I would never walk again. My mother told me I would. I believed my mother."
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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