Inspiring: People with Disabilities News Stories
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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 dont 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 childrens 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 theyre 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 citys 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 laws 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 Heumanns 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.
Note: Listen to a BBC interview with this courageous, pioneering woman. Explore a treasure trove of concise summaries of incredibly inspiring disabled persons news articles which will inspire you to make a difference.
When Trinity Jagdeos 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 couldnt 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. Trinitys 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 didnt 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 Trinitys 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 Amazons publishing tools. I put the entire thing together, and theyd 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 Alexuss 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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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 wasnt 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 USAs 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 didnt 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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There is something different, and a little special, about Universo Santi, a restaurant in the southern Spanish city of Jerez. People dont come here because the staff are disabled but because its 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 Fundacin 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 Bazn, head of human resources, who has cerebral palsy. Its 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 Gimnez, 23, has Downs syndrome and is a commis chef. Its given me the chance to become independent doing something Ive loved since I was a kid, says Gimnez, 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 didnt even know how to take a train by myself because Id just miss my stop. Since it opened in October 2017, Universo Santi continues to win plaudits for its cuisine.
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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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When Charles King went blind at 39, he gave up on life, on his pregnant girlfriend, and on himself. I said OK God, thats 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 wasnt the toughest battle King would have to face. In 2000, after he got clean and was reunited with his family, Kings 14-year-old daughter died. Five years after that, he was diagnosed with cancer. And yet, somehow hes 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 hed 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 its too hard, but after watching you, Im regenerated, King recalled. I said, Son, God blessed both of us today.
Note: Watch a moving video of this inspiring man talking about his profound transformation. Explore a treasure trove of concise summaries of incredibly inspiring disabled persons news articles which will inspire you to make a difference.
[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 troupes 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 Devices creative director and choreographer, told NBC News. Before Downs 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 didnt plan to work with artists with Downs 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 whats 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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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 Caint Say No. I find it to be fascinating that often people dont think I can dance, she said. Who says that dance isnt turning on wheels? Who says dancing isnt throwing your arms up in the air and grabbing someone elses 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. Im very aware that when I was a little girl I wasnt seeing anybody like me, and on days when Im 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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Two pedals, one leg - the bicycle and Emmanuel Ofosu Yeboah werent exactly made for each other. He got on one anyway, and it changed his life. Changed other peoples 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 werent making fun of him. They were cheering. By the time he was done, hed 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, Emmanuels Gift, narrated by Oprah Winfrey. And then the publics attention moved on, as it always does, to other dreams, to other dreamers. Except Yeboah isnt finished with his. He wants to build a school in Ghana for the disabled. So hes formed a nonprofit organization, Emmanuels Dream. But he also knows what got him noticed in the first place. Hes 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.
19-year-old Gabe Adams was born with Hanhart syndrome, a rare medical condition characterised by underdeveloped limbs, mouth and jaw. In Gabes 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 handicappedand 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. Im Palestinian, Muslim, Im a woman of color, Im 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 countrys 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 Zayids show could crush enduring stigmas disabled people face.
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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. Thats 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. Thats what I really loved about it. You can feel all these little knobs and cracks and fissures and little dishes in the rock. So youre 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 youre trying to solve this puzzle thats 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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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.
Note: For more on the incredibly inspiring story of this great man, read this engaging article. Explore a treasure trove of concise summaries of news articles on incredibly inspiring disabled persons.
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.
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.
Note: Don't miss the incredibly inspiring one-minute video of this inspiring blind artist.
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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If you had asked me 20 years ago where I would be, I never would have imagined I would be a physician working at UCLA Health, one of the best medical centers in the country. For over 25 years, my physical disability threatened to define who I was and what others thought I could become. I contracted meningococcal disease at 8 years of age. The infection overwhelmed my body's defenses, and I became a triple amputee. The disease left me with just enough to survive and carry on: two full fingers of the left hand, the thumb and ring finger. The first few years were physically and emotionally grueling; I was in and out of the hospital for surgical procedures to make my lower limbs fit better into prosthetic legs. I couldn't walk for nearly three years. I grew so quickly, my prosthetic legs could not keep up. My father would give me piggyback rides from the car to our house. My mother, who became blind as a teen, learned how to help me dress and put on my prosthetic legs every morning for school. My younger brother, Tarring, would help bring things to me since my mobility was limited. And my older sister, Nellie, was and is my inspiration and role model. I have been extremely lucky to have a strong and resilient family. I was lucky to be in a place where I had great medical care and where I had a community of friends and schools that supported my recovery and believed in my ability to succeed despite my disability. But luck is only part of my success; it takes courage, determination, honesty and integrity to pursue your dreams.
Note: Dr. Kellie Lim, author of this article received her medical training from the David Geffen School of Medicine at the University of California, Los Angeles. After getting her medical degree, she completed her residency in pediatrics before pursuing fellowship training in allergy & immunology and pharmacology. Today, she works as an allergist-immunologist at UCLA Health. Explore a treasure trove of summaries of news articles on incredibly inspiring disabled persons.
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