Inspiring Disabled Persons News ArticlesExcerpts of key news articles on inspiring disabled persons
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."
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.
Scaling Everest requires the enthusiasm and boosterism of a physical-education teacher combined with the survival instinct of a Green Beret. You have to want that summit. Erik Weihenmayer, 33, wasn't just another yuppie trekker. Blind since he was 13 ... he began attacking mountains in his early 20s. For Erik ... excelling as an athlete was the result of accepting his disability rather than denying it." Climbing with Erik isn't that different from climbing with a sighted mountaineer. You wear a bell on your pack, and he follows the sound ... using his custom-made climbing poles to feel his way along the trail. His climbing partners shout out helpful descriptions: "Death fall 2 ft. to your right!" Almost 90% of Everest climbers fail to reach the summit. Many – at least 165 since 1953 – never come home at all. When Erik and the team began the final ascent from Camp 4 ... they had been on the mountain for two months ... getting used to the altitude and socking away enough equipment [before they made the final, successful] summit push. "He was the heart and soul of our team," says Eric Alexander. "The guy's spirit won't let you quit." It could be called the most successful Everest expedition ever, and not just because of Erik's participation. A record 19 climbers from the N.F.B. team summited, including the oldest man ever to climb Everest – 64-year-old Sherman Bull. Perhaps the point is really that there is no way to put what Erik has done in perspective because no one has ever done anything like it. It is a unique achievement, one that in the truest sense pushes the limits of what man is capable of.
Note: Don't miss the entire inspiring blind to failure story at the link above. And check out an awesome video highlighting many of Erik's wild adventures.
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."
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.’
Note: Don't miss the incredibly inspiring video at the link above. Explore a treasure trove of concise summaries of incredibly inspiring disabled persons news articles which will inspire you to make a difference.
Seventeen-year-old Gabe Adams was born without arms and legs and suffers from a rare disease called hanhart syndrome, but that doesn't stop him from dancing. After spending most of his life in a wheelchair, he decided to join the dance team at Davis High School. During halftime at a basketball game Friday night, he performed in front of the whole school. Cheers rang out as Gabe put the word disability to shame. "I wanted to prove to myself and to others that there’s more to myself than just a kid in a wheelchair," Adams said. With practices three days a week, which last for more than three hours, dance team is no easy commitment. However, teammate Alexis Delahunty says Gabe makes it seem easy. "I can’t even imagine doing this without my arms and legs. It's so inspiring. He’s just amazing," Delahunty said. His dance teacher, Kim King, says Gabe has brought so much joy to the team and has pushed them all to work harder. "When they see him, they don’t realize how hard it is to get dressed, how hard it is to get in and out of his chair, but Gabe does everything by himself," King said. Gabe's father, Ron Adams, said Gabe is always pushing himself and taking each challenge in stride. "I don’t think everyone understands what it takes, the muscle coordination and development to balance when he doesn’t have limbs," Ron Adams said. He may not realize it, but Gabe is constantly inspiring the people around him.
Note: Note: Don't miss the amazing video at the link above. For more on this most impressive teenager, see this story. Explore a treasure trove of concise summaries of news articles on incredibly inspiring disabled persons.
Most children want to dress up for Halloween, but for those confined to wheelchairs, it isn’t always that simple. Ryan Weimer understands that concept better than most. When his oldest son, Keaton, was 3 years old, he told his dad he wanted to be a pirate for Halloween. Instead of simply dressing him up, Weimer spent months building Keaton - who lives with muscular dystrophy - a pirate ship made of wood, tablecloth sails and specially-crafted cannons, all fitted to his wheelchair. Keaton was ecstatic - and his dad never forgot the feeling. "When you know that you have few memories to make with your kids, you want to make priceless ones," Weimer told NBC News, "and epic ones." His second son, Bryce, also lives with muscular dystrophy. Over the years, their wheelchair costumes have gotten more elaborate and attracted more attention. And this year, the Weimer family project became a hugely successful non-profit, called Magic Wheelchair. Volunteers from around the country donated their time, talents and resources to create dream costumes for eight lucky children — six from Weimer’s home state of Oregon and two from Georgia. "When we have challenges and trials and hard times, those are the things that define us," Weimer said. "It doesn’t' matter your circumstances, you can still make beautiful things ... and it's great to see other people get behind that."
Note: Don't miss this very touching video on Magic Wheelchairs.
In 1978, 5-year-old Frank "Bopsy" Salazar was diagnosed with leukemia. A woman named Linda Pauling ... had lost her 7-year-old son, Chris, to leukemia that spring. But before Chris passed, the Arizona Department of Public Safety had fulfilled the little boy's dream of becoming a police officer. DPS officers Jim Eaves and Frank Shankwitz had met Chris with a patrol car and motorcycle and made him the only honorary Arizona Highway Patrol Officer in the department's history. The incredible effort inspired Pauling and Shankwitz to start the Make-A-Wish Foundation. "[Pauling] told me that instead of letting the kids just feel sorry for themselves, they wanted to grant wishes, to do something every kid would benefit from, to fulfill their dream while they're still a part of this world," Trujillo said. Shankwitz took over from there, and he went to visit Bopsy to find out more about the boy's dreams. After learning that he'd be granted a wish, the 7-year-old mulled it over. "I want to ride in a hot air balloon," he told Shankwitz. Then he thought about it some more. "No, I want to go to Disneyland." He paused again. "No, I want to be a fireman." But Shankwitz didn't make him pick. All of Bopsy's wishes would be granted. He got his balloon ride and his trip to Disneyland. Fireman Bob - whose real name is Bob Walp - did more than was asked of him to help the sick boy. "We didn't want to just give him a tour," Walp [recalled]. "We decided to give him a badge and a jacket. We let him use the hose. We took him in the truck."
Note: For more on this inspiring story, see this webpage.
When she was in high school, Lizzie Velasquez was dubbed "The World's Ugliest Woman" in an 8-second-long YouTube video. Born with a medical condition so rare that just two other people in the world are thought to have it, Velasquez has no adipose tissue and cannot create muscle, store energy, or gain weight. She has zero percent body fat and weighs just 60 pounds. In the comments on YouTube, viewers called her "it" and "monster" and encouraged her to kill herself. Instead, Velasquez set four goals: To become a motivational speaker, to publish a book, to graduate college, and to build a family and a career for herself. Now 23 years old, she's been a motivational speaker for seven years and has given more than 200 workshops on embracing uniqueness, dealing with bullies, and overcoming obstacles. She's a senior majoring in Communications at Texas State University in San Marcos, where she lives with her best friend. Her first book, Lizzie Beautiful, came out in 2010 and her second, Be Beautiful, Be You, was published earlier this month. She's even reclaimed YouTube, video blogging about everything from bullying to hair-styling tips to staying positive. Of course, the horrible comments left on that old YouTube video stung. "I'm human, and of course these things are going to hurt," she said. "Their judgments of me isn't who I am, and I'm not going to let these things define me. I didn't sink down to their level," she said in a follow-up video on YouTube last year. "Instead, I got my revenge through my accomplishments and determination. In the battle between the 'World's Ugliest Woman' video vs. me, I think I won."
Note: Though looking at this woman can be disturbing for some, consider that you can see beneath the surface to the beauty within. Watch Lizzie share some of her wisdom in a popular TEDx Talk at this link.
When I met 18-year old Patrick Henry Hughes, I knew he was musically talented. I had been told so, had read that he was very able for someone his age and who had been blind and crippled since birth. Patrick's eyes are not functional; his body and legs are stunted. He is in a wheelchair. When we first shook hands, his fingers seemed entirely too thick to be nimble. So when he offered to play the piano for me and his father rolled his wheelchair up to the baby grand, I confess that I thought to myself, "Well, this will be sweet. He has overcome so much. How nice that he can play piano." But then Patrick put his hands to the keyboard, and his fingers began to race across it -- the entire span of it, his fingers moving up and back and over and across the keys so quickly and intricately that my fully-functional eyesight couldn't keep up with them. I was stunned. The music his hands drew from that piano was so lovely and lyrical and haunting, so rich and complex and beyond anything I had imagined he would play that there was nothing I could say. All I could do was listen. "God made me blind and didn't give me the ability to walk. I mean, big deal." Patrick said, smiling. "He gave me the talent to play piano and trumpet and all that good stuff." This is Patrick's philosophy in life, and he wants people to know it. "I'm the kind of person that's always going to fight till I win," he said. Patrick also attends the University of Louisville and plays trumpet in the marching band. The band director suggested it, and Patrick and his father, Patrick John Hughes, who have faced tougher challenges together, decided "Why not?" "Don't tell us we can't do something," Patrick's father added, with a chuckle. He looks at Patrick with a mixture of love and loyalty and admiration, something not always seen in the eyes of a father when he gazes at his son. "I've told him before. He's my hero."
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.
Amber Miller accomplished two monumental feats this weekend. Days from her due date, the 27-year-old joined 45,000 other runners to participate in Sunday's Bank of America Chicago Marathon and then gave birth to a baby girl named June hours later. Miller, an avid runner, said she signed up for the 26.2-mile race before finding out she was pregnant. She said she never expected to finish the race. "I was having a conversation with my parents and said, 'You know what? I have no plans of actually finishing,'" she told reporters at Central DuPage Hospital this morning. "I was planning on running half, skipping to the end, then walking across the finish line." But Miller and her husband started running, and just kept going. They ran part of the race and walked the second half as her contractions started. It took the couple 6.5 hours to finish. She said she grabbed something to eat and the two headed to the hospital. "It was very interesting hearing people's reaction," Miller said about crowds watching an extremely pregnant woman among the runners. "I've been running up to this point anyway, so I'm used to it." At 7 pounds, 13 ounces, baby June entered the world at 10:29 p.m. Sunday, just hours after her parents crossed the finish line.
Reaching the summit of Mount Everest is a triumph for any climber, but for Erik Weihenmayer, the accomplishment is even more impressive. That’s because he is blind. Born with a rare eye disease, Mr. Weihenmayer lost his sight at age 13 and later discovered a sense of freedom through climbing. Over the years, the 50-year-old has reached the highest peaks on seven continents and also kayaked the Colorado River through the Grand Canyon. A former schoolteacher, Mr. Weihenmayer co-founded No Barriers, a nonprofit organization that teaches outdoor skills to those with physical challenges. "Growing up in Connecticut, my Dad would drive me three hours to Massachusetts once a month to this adventure program for the blind, [said Mr. Weihenmayer]. "They took us to New Hampshire and we rock climbed on these beautiful granite rock faces. It was very tactile. That’s what I really loved about it. You can feel all these little knobs and cracks and fissures and little dishes in the rock. So you’re problem-solving with your hands and feet as your eyes. You had to put your body in all these cool, acrobatic positions to get yourself from point A to point B and you’re trying to solve this puzzle that’s embedded in the rock. I loved the great adventure. I got to the top and I could hear the valley below me. I could hear the wind blowing through the trees. And I thought this is so stunning. This is what I want out of my life."
Note: Explore a treasure trove of concise summaries of incredibly inspiring disabled persons news articles which will inspire you to make a difference.
Kanya Sesser, 23, skateboards, models lingerie and surfs – and she does it all without lower limbs. Sesser, who was born without legs, was adopted from an orphanage in Thailand before moving to Portland, Oregon, with her new family. Now, she earns more than $1,000 a day working as a model. "I enjoy making money from it and I love showing people what beauty can look like," Sesser told the Daily News. "These images show my strength." The 23-year-old, who uses a skateboard instead of a wheelchair, began modeling for sports brands when she was 15. The Huffington Post UK reports that the Los Angeles-based model has reportedly posed for brands like Billabong, Rip Curl Girl and Nike. "I was mainly doing athletics shoots then as I got older I got into lingerie modeling," Sesser told the Daily News. "It's something fun and it shows my story – I'm different and that is sexy, I don't need legs to feel sexy." Now, the model hopes to compete in the 2018 Winter Paralympics in Pyeongchang, South Korea, as a mono-skier.
Note: Don't miss this inspiring seven-minute video of Kanya's courage and fascinating life.
Jessica Cox was born without arms as a result of a rare birth defect. That has not stopped her from living her life to the fullest. In fact, Ms Cox has experienced and achieved more than most people do in a lifetime. She can drive a car, fly a plane and play piano - all with her feet. In 2012 she married Patrick, her former Taekwondo instructor (she has two black belts). They live in Tucson, Arizona. Ms Cox, 30, travels around the world as a motivational speaker, using her own life as an example of what one can achieve if one wants it enough. This month she visits Ethiopia to help promote disability rights.
Note: Don't miss the inspiring video on the BBC webpage. And for another incredibly inspiring man born without arms or feet, learn about Nick Vujicic at this link.
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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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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The newest resident of "Sesame Street" has orange hair and a fondness for her toy rabbit. She also has autism. Julia has been a part of the "Sesame Street" family via its storybooks and was so popular that the decision was made to add the character to the TV series. "I think the big discussion right at the start was, 'How do we do this? How do we talk about autism?,'" one of the show's writers, Christine Ferraro, told "60 Minutes" correspondent Lesley Stahl. Over the almost five decades "Sesame Street" has been on the air, it has established a reputation for inclusion with its characters. Joan Ganz Cooney, one of the founders of the Children's Television Workshop which developed "Sesame Street," said it has also not been afraid to deal with real life issues. Julia's debut episode will deal with what autism can look like. The brain disorder can make it difficult for people with autism to communicate with and relate to others. The character of Big Bird talked to Stahl about his first interaction with Julia in which she ignored him. "I thought that maybe she didn't like me," he said. "Yeah, but you know, we had to explain to Big Bird that Julia likes Big Bird," the Elmo character added. "It's just that Julia has autism. So sometimes it takes her a little longer to do things." Ferraro hopes that along with educating viewers about autism the new character will settle in as a part of the neighborhood. "I would love her to be not Julia, the kid on Sesame Street who has autism," the writer said. "I would like her to be just Julia."
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Andrew Short lives with spastic cerebral palsy, which he contracted during birth. Cerebral palsy is a disorder that effects muscle tone, movement and motor skills, but despite impaired speech Andrew’s disability doesn’t impair his mind, and he learned to read early. “I speak three languages,” said Andy. “English, German, and spastic. Spastic is my mother tongue." Andrew is currently completing a Masters Degree in Disability Studies, but his most impressive achievement has been walking the Kokoda Trail, which he describes as “the toughest physical challenge of [his] life”. In Andy’s late twenties, his motor function appeared to begin deteriorating. “We were told to accept that that's what it would be,” said [Andrew's father] David. Instead, David and Andrew began researching the emerging field of neuroplasticity ... inspired by the seminal [book], “The Brain That Changes Itself: Stories of Personal Triumph from the Frontiers of Brain Science”. Andrew’s physical condition is due in part to his trainer, Lee Campbell, a former army trainer and Sydney Swans team member. The two have been training together for five and a half years, and in that time Lee estimates that his physical condition has risen from 2.5 to a 7 or 8. “You watch Andy pull a sled with 20 or 30 kilos of weights in it, he stands up, his posture is corrected,” said Lee. “His finer motor skills now are getting refined. He can hold things, he can cook, he can do his buttons up.” Right now, they’re training together for Andy’s next endeavour, walking the Great Wall of China.
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“People always say to me, ‘Anyone who runs as much as you do deserves to be skinny.’ Of course, what they're really saying: ‘If you do all this running, why are you still so fat?’” Early that morning [Mirna] Valerio had led a three-mile group run around the campus of Rabun Gap-Na-coochee School in the nearby town of Rabun Gap, where she serves as Spanish teacher, choir director, and head coach of the cross-country team. She's about to start her second run of the day. Every run, every race, every traverse of a mountain trail, every gym workout, Valerio begins by taking a photo. “To prove that I was out here,” she explains. Later, she will post the photos on ... her blog, Fat Girl Running, in which she both writes of the joys of the running life and thoughtfully, humorously, and sometimes angrily rebuts her doubters, who can't believe that a self-described fat person might discover - or deserve - this kind of joy. With a BMI ... above the National Institutes of Health-established line defining obesity, Valerio, a marathoner, ultramarathoner, and trail runner, has emerged as ... a living argument that it's possible to be both fit and fat. “I'm pretty much in love with my body,” she writes. “Sometimes I get disappointed or angry with it, but like any long-term, committed relationship, it usually comes right back to love and respect.” By making peace with her obesity - or, more accurately, by fighting her disease to a kind of enduring, vigorously active truce - Valerio draws kudos from a formerly skeptical medical community.
Note: Read another great piece on this inspiring woman.
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