Inspiring: People with Disabilities Media Articles
Below are key excerpts of inspiring news articles on people with disabilities from reliable news media sources. If any link fails to function, a paywall blocks full access, or the article is no longer available, try these digital tools.
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There was a lot that Army veteran Alex Dillman lost when he became a paraplegic after an IED blew up under his legs in Afghanistan, but now an unlikely activity has allowed him to take some of what he lost back. Hurtling through the air at 120 mph, Dillman doesn’t need his wheelchair to skydive; he doesn’t really need his legs either. In that unique state of concentration and freedom, he says he’s “expected to perform,” a do-or-die state of mind that he says he hasn’t felt since his old life on deployment. Dillman originally saw adventure therapy as a way to combat depression and PTSD he suffered from in the wake of his lost abilities, but he never imagined it would help him get some of those abilities back. Now he’s part of an adventure therapy non-profit called Skydive First Project, where he utilizes outdoor adventures to assist individuals suffering from PTSD and depression. Based in Tampa, activities encompass hiking, kayaking, rock climbing, horseback riding, scuba diving, and tandem skydiving. “[The] great thing about skydiving is that it gets me out of the chair,” said Dillman. “I don’t bring my chair with me, so I’m in a free state. I don’t need to be in the chair to perform the act of skydiving.” “I can feel my legs and my feet to a certain extent. I can get a better sense of my overall being, feel what my legs are doing, feel what my hips are doing. Having that feeling again ... even if it’s for 30 seconds or 60 seconds ... is enough for me!”
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Faith Snapp has never let her blindness get in the way of pursuing her dreams. A 22-year-old Texas native who is legally blind, Snapp was accepted into the Texas Tech University School of Veterinary Medicine. “My entire life, my family has raised horses and goats for as long as I can remember,” Snapp shared. “I always loved animals.” Snapp and her twin brother were both born prematurely — and with very limited vision. Snapp has had a guide dog since high school, but she has never let her disability come across as a limitation. She was in several clubs in high school and even worked at local animal clinics. While her blindness may have been a challenge at first, she “needed” people to come alongside her and support her dreams. “I just needed to find the people and the accommodations and the places that would be willing to help me,” the 22-year-old student [said]. “That was a little bit challenging because I think oftentimes people place limitations on somebody with a disability because they assume that they are limited.” Snapp will begin classes in August, and hopes to pursue a career as a mixed-animal veterinarian, working with both large and small animals. It doesn’t matter what challenges a person may be facing, Snapp said; people should not give up on their dreams. “No matter who you are or what your circumstances… anything is possible,” she said. “I just hope my story can help others realize that you can accomplish anything you set your mind to.”
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From a Tampa performing arts conservatory comes the story of a blind jazz saxophonist who uses his disability as a teaching tool. He encourages his students to act on instinct; to feel the music through their instruments, and not let the waking world deceive them. “Welcome to every day of my life,” says Matthew Weihmuller in his jazz improvisation class after turning the lights off. “Then we have a big laugh,” he adds. When Weihmuller started playing, he needed braille sheet music, and pieces would take months; even years to learn. As if that weren’t difficult enough, few people in the country were capable of providing braille music, so he started “brailling” his own, with the help of his mom. “They can’t look at their instrument. Now, they have to feel their instrument with their fingers and hands, right?” Weihmuller told Fox 13. “Now, we’ve got to listen to the music. We can’t read it. It forces the students to use their other senses.” During improvisational sessions, a musician has to be ready for sudden changes in time signature or key. This is nearly impossible to express through sheet music. At least in this regard, the children are learning in the best way for this unorthodox, yet traditional form of jazz music. As an educator with blindness, Weihmuller stresses turning any disadvantage into an advantage, a teaching philosophy that has led some students to tell the man that he has changed the way they look at life.
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On a sunny March morning in Bengaluru, Ayesha Banu and Noorunnisa walk up to the stage of Nitte Meenakshi Institute of Technology. Their white canes folded and held aside, they speak to a packed hall of students and teachers about their work as Medical Tactile Examiners (MTEs). "We assist doctors in detecting the early signs of breast cancer in women," Banu speaks into the mic. "Using the first two fingers of both hands, we examine women's breasts for abnormalities." She explains that blind women like herself and Noorunnisa are especially well-suited to this profession because of the "high tactile sense in our fingertips, which helps us find tiny lumps in the breast." Tactile breast examinations, or TBEs, are clinical breast examinations specially designed for blind women trained as MTEs. Employing MTEs for routine breast cancer screening – and reaching women in their communities and workplaces – could help in the early detection of cancer and save lives, says Dr. Poovamma CU, the breast specialist under whom Banu and Noorunnisa work. Studies prove that in the absence of sight, blind people's brains can develop a heightened sense of touch, as well as hearing. Through the MTE training, a woman with vision impairment is able to empower another woman, by offering her preventive health care. In a recent Indian study where two MTEs conducted TBEs on 1,338 women, their success rate of detecting malignant cancers was over 78 percent, and the miss rate, only one percent.
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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.
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A patient who was left almost completely paralyzed from a rare disease is now walking and talking again, after a music therapist prescribed mindful listening to his favorite song every night–in this case, a tune by The Carpenters. 71 year-old Ian Palmer was struck down with Guillain-Barr© syndrome last June, forcing him to spend seven months in a hospital where he was unable to walk or speak properly. The rare condition happens when a person's own immune system attacks their body's motor nerves, causing muscle weakness and sometimes paralysis. But when Ian was transferred to Sue Ryder Neurological Care Centre, a state-of-the-art care unit in Lancashire, England, clinicians used music therapy techniques to overcome 'near total paralysis of his body'. His specialist, Clare, taught him mindfulness techniques using his favorite records–and he began listening to The Carpenters each night. Ian was admittedly skeptical, but he can now walk 2 miles a day (3k) and have conversations with his family after the exercises "opened up" his brain. He's never been very musical, so when Sue Ryder first suggested music therapy he said, 'What good is that going to do?' "I'm a typical Northern man, and I thought, 'What's a girl with a guitar going to do for me–get me to the gym.'" "But it really worked. Clare sat me down and explained the process. I learned that music is very unlike other therapies, as it opens up all of the brain."
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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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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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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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In 2011, [Ropert Kapen] suffered a brain stem stroke that left him paralyzed. Doctors told his family that he had a 1% chance of survival, and that if he lived, he'd likely be in a vegetative state. Kapen beat those odds. His mental faculties were unscathed, and he slowly regained some movement and speech through therapy. Eventually, he was able to communicate, eat, operate a motorized wheelchair and write a book. He had another big dream, too. "Growing up, I fell in love with hiking, being outdoors and the beauty of nature," he says. That was taken away from him for 10 years, Kapen says, but very recently, a new set of wheels has allowed for his return. It's called the AdvenChair [which] recently enabled Kapen to visit Machu Picchu. The orange, "all-terrain" wheelchair is human-powered and designed to help people with mobility challenges to venture into the wild. Its wheels, tires, brakes and handlebars are all premium mountain bike parts, and the large tires and suspension system offer a comfortable ride. Thanks to a versatile system of pulleys, bars and straps, teams of one to five people can assist in navigating the AdvenChair over just about any landscape. "It's rejuvenating to be outside, especially as a person with a disability, because these resources are not exactly the most accessible," [Isaac] Shannon says. "So when there is a tool that allows a person to be able to experience life in the most average way possible, I think it's healing, and it's nice to be out in nature where you're not around people."
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From Hawaii to Bali and the ski-slopes of Perisher, 26-year-old Jimmy Antram has seen plenty of the world. But it has all been from the vantage point of his mother's back. Fulfilling a promise she made to herself as a 17-year-old first-time mum to give her disabled son the best life she possibly could, Niki Antram has spent years travelling the globe with Jimmy clinging to her shoulders. Jimmy was born with physical and mental disabilities, including blindness, and requires round the clock care from Ms Antram and his support workers. He has a wheelchair, but Ms Antram has never enjoyed using it. She's content to carry him while she's physically able and helps him walk short distances on his own. Incredible photographs taken around the globe show him clinging on as they hike through mountains and rainforests. 'Planning big holidays, I always make sure I have plenty of nappies, clothes, and even bed pads, sheets and pillowcases,' she [said]. Ms Antram plans a meticulous itinerary and calls ahead for every venue she wants to visit - whether it be a restaurant, hotel or daredevil adventure. 'Even if I know we will be okay I like to inform the companies to give them a heads up about us to make sure they understand and are okay with having us there,' she says. Sometimes, they can't accommodate. This is usually because of risks associated with Jimmy's condition or logistical difficulties. Ms Antram said the exception to this was in Hawaii, where 'everyone wanted [Jimmy] to join'.
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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 Éléonore 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 Frédéric 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. “Eléonore 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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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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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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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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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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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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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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