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Planet Earth
Joined March 2014
Photo by Thinking Humanity (@ThinkingHumanit)Photo by Thinking Humanity (@ThinkingHumanit)Photo by Thinking Humanity (@ThinkingHumanit)Photo by Thinking Humanity (@ThinkingHumanit)Photo by Thinking Humanity (@ThinkingHumanit)Photo by Thinking Humanity (@ThinkingHumanit)Photo by Thinking Humanity (@ThinkingHumanit)Photo by Thinking Humanity (@ThinkingHumanit)Photo by Thinking Humanity (@ThinkingHumanit)Photo by Thinking Humanity (@ThinkingHumanit)
In 2014, a young Japanese footballer named Ryota Iwaoka had the rare chance to meet one of the world’s greatest players, Cristiano Ronaldo, at a special event. Determined to make the moment count, Iwaoka decided to ask Ronaldo a question in Portuguese — a language he was still learning. He practiced diligently with his coach beforehand, hoping to get it right. Standing before a large crowd, the nervous teenager asked Ronaldo how he could become a professional footballer. However, as he spoke, he stumbled over some words and pronunciation. A few people in the audience began to laugh, leaving Iwaoka visibly embarrassed. Ronaldo immediately stepped in to support him. He told the crowd to stop laughing and praised the young player for his effort. “Why are they laughing?” Ronaldo said. “You speak good Portuguese. They should be happy because you tried very hard.” Ronaldo then offered Iwaoka some simple but powerful advice: believe in yourself, work hard, and never miss an opportunity. Those words left a lasting impression on the young player. Inspired by the encounter, Iwaoka continued chasing his dream with renewed determination. He worked tirelessly to improve his skills and eventually played as a midfielder for Yamanashi Gakuin University. His dedication paid off in 2020, when his team won Japan’s national university soccer championship. What started as a nervous question to his idol became a defining moment that helped Iwaoka keep believing in himself and pursuing his goals.
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A five-year-old boy desperately needed a stem-cell donor. So 4,855 strangers stood in the pouring rain to see if they could save him. 💛 Oscar Saxelby-Lee, from Worcester, England, was diagnosed with aggressive T-cell acute lymphoblastic leukemia in December 2018. His family urgently needed to find a compatible stem-cell donor. In March 2019, Oscar's school opened its doors for a DKMS registration drive — and something extraordinary happened. People came by the thousands. For two days, 4,855 potential donors queued in the rain to have their cheeks swabbed. It became the largest donor-registration event DKMS UK had ever held, more than doubling its previous record of 2,260 people. A compatible donor was found, and Oscar received treatment including a stem-cell transplant. For a while, there was hope. Then the leukemia returned. Doctors in Britain eventually exhausted the available conventional treatments. Oscar's parents, Olivia and Jamie, refused to stop searching. They raised more than £500,000 and took him thousands of miles to Singapore, where doctors at the National University Hospital offered an experimental CAR-T cell treatment for his rare leukemia. On Christmas Eve 2019, Oscar received the therapy. Weeks later, tests found no detectable leukemia cells in his blood. By June 2020, he had remained cancer-free for six months and was finally able to return home. Later reporting confirmed that Oscar remained in remission. His story is extraordinary because of the medicine that saved him. But also because of what happened before it. 4,855 people stood in the rain for a little boy most had never met. None knew whether they would be his match. They only knew there was a chance. And they showed up. ❤️ Sources: DKMS UK; National University Hospital Singapore; Channel NewsAsia; ITV News.
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Dementia changed their routines. Jay Leno keeps finding ways to share life with his wife. 🚗❤️ Jay and Mavis Leno married in 1980. Decades later, caring for her through advanced dementia has brought profound changes to their days together. In a November 2025 interview with Hoda Kotb on TODAY, Jay said restaurant outings had become difficult. Instead, with help, they take Mavis out in the car to look around — something he said she enjoys. Travel has changed, too. They watch travel videos and animal shows together, bringing glimpses of the wider world into their home. Jay also described using humor to make everyday care gentler. When carrying Mavis to the bathroom, he jokes that they are at a high-school prom and sways with her, making her laugh. “When she looks at me and smiles and says she loves me, I melt.” Their story holds both affection and the sadness of losing familiar experiences. It also includes help: devotion doesn’t have to mean facing every challenge alone. Sometimes love looks like changing the plan so you can still spend time together. Sources: TODAY interview, November 20, 2025; Us Weekly, November 20, 2025. Photo: Amy Sussman/Getty Images (2024).
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They ignored the “DO NOT PARK” signs… and came back to their cars covered in cow slurry. 💀🚜 Dozens of drivers parked on private farmland near Rydal in the Lake District, ignoring clear warning signs and barriers. When they returned, their vehicles (including luxury cars) were absolutely splattered with cow slurry. The farmer had finally had enough. Police are now making enquiries, but the internet is divided: some are calling it perfect countryside karma, others say the farmer went too far. Was this fair punishment for trespassing and disrespecting private land… or did he cross the line?
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Do you know what this strange object is? 🤔👇
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How old is Linda? 🧠 Take your time with this one! Another viral math puzzle has people debating the answer. See how this different challenge works and test your reasoning.
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It's pretty obvious why... 👇
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Susan Schneider first met Robin Williams at an Apple store in 2007. She later remembered, "I walked in and saw this man and I thought, 'I think that's Robin Williams.' Then, on my way out, I happened to look at him again, and he was smiling at me, and something inside me said, 'Oh, just go over and say hi.' He was wearing camouflage print, so I said, 'How's that camo working out for you?' And he said, 'Not too good — you found me.'" The pair soon fell in love, and they later got married in 2011 in Napa Valley, California. But tragically, just two years later, Williams began to suffer from a myriad of physical and mental health issues. Plagued by tremors, insomnia, delusions, stomach problems, paranoia, depression, vision problems, and more, Williams confessed to Schneider that he felt that he was "losing his mind" and that he needed a "reboot for his brain." In May 2014, Williams was diagnosed with Parkinson's disease, but he didn't feel that the diagnosis explained all his symptoms — and tragically, he was right. After Williams died by suicide in the couple's California home in August 2014, Schneider learned from the doctors who examined him that he had been misdiagnosed with Parkinson's and actually had the brain disease Lewy body dementia. Shockingly, experts said his condition was so severe that they were surprised he was able to walk or move at all. Learn more about Susan Schneider's relationship with Robin Williams — and her mission to educate the public about his condition 👇
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Evan Spiegel, the CEO of Snap, and his wife, model Miranda Kerr, have made a remarkable donation that will change the lives of hundreds of thousands of people in California. ❤️ Through a multimillion-dollar gift to the nonprofit Undue Medical Debt, they have helped erase $550 million in medical debt for more than 261,000 Californians. This relief is being distributed across the state, with many people receiving letters informing them that their debt has simply disappeared — no application required. 💌 The impact is especially large in certain counties. In San Diego County alone, $99 million in medical debt has been wiped out for over 40,000 residents. 🏥 In Los Angeles County, $26.7 million was erased for more than 17,000 people. Other counties across California are also benefiting from the donation. Undue Medical Debt uses donated funds to buy medical bills in bulk at a fraction of their original value, then forgives them completely. This model allows relatively modest contributions to create enormous relief for families struggling with healthcare costs. For many recipients, this means freedom from overwhelming bills that can damage credit, cause stress, and limit opportunities. It offers a real chance to move forward without the constant weight of medical debt hanging over them. 🌱 In a time when healthcare costs continue to burden millions of Americans, this act of generosity stands out as a powerful example of how targeted philanthropy can directly improve lives on a large scale. Sources: Los Angeles Times, Undue Medical Debt official announcement, Fortune
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Amy Jandrisevits spent years working as a pediatric oncology social worker, where she learned how powerful play could be for children facing frightening medical experiences. But she noticed something missing: The dolls children were given rarely looked like them. ❤️ So in 2014, from her dining-room table in Wisconsin, Amy began creating “A Doll Like Me.” Every doll is individually handmade to resemble the child receiving it. She studies photographs and family descriptions to recreate the details that make each child unique. Some dolls have limb differences or prosthetics. Others have feeding tubes, surgical scars, birthmarks, albinism, vitiligo or other visible differences. The idea is beautifully simple: every child deserves to see themselves represented in the toys they love. Amy's background in social work shaped the project. Dolls are frequently used therapeutically because children can use play to communicate emotions they may struggle to express in words. A personalized doll can become more than a toy—it can provide familiarity, comfort and a way to process feeling different. Each doll takes hours to create and costs roughly $70–$100 in materials and labor, but donations and sponsorships have helped Amy provide dolls to families regardless of their ability to pay. The reactions can be extraordinary. One mother described her nonverbal son's response to receiving his look-alike doll as “pure joy.” What started at one woman's dining-room table has grown into a nonprofit project sending personalized dolls to children around the world. Amy's philosophy remains beautifully straightforward: “In an ideal world, limb difference, body diversity, ethnicity and medical differences would be as represented in dolls as they are in real life.” Sometimes inclusion begins with something as small as a child looking at a toy and realizing: That one looks like me. ❤️ Sources: A Doll Like Me; CBS News; TODAY; Good Morning America; GoFundMe.
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Meet Jonathan, one of nature’s most remarkable living legends. This Seychelles giant tortoise is believed to be approximately 194 years old, making him the oldest known living land animal on Earth. Born around 1832, he arrived on the remote island of Saint Helena in 1882 and has lived peacefully on the grounds of Plantation House ever since. Just look at these powerful photos — one from 1942 and one from recent years. Jonathan has quietly witnessed the world transform beyond recognition, living through eras before widespread electricity, cars, airplanes, world wars, and the internet, all the way into 2026. Recognized by Guinness World Records, he continues to thrive today — a beautiful reminder of patience, resilience, and the extraordinary longevity found in the natural world. 🐢 How does it feel to look at a being who has seen so much of our history unfold? #JonathanTheTortoise #OldestLivingAnimal #NatureWonder
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They thought they were catcalling women out for a casual run. In reality, they were harassing undercover police officers. 👀🏃‍♀️ In Surrey, England, female officers dressed as joggers patrolled areas with repeated reports of street harassment. Backup teams remained close by but out of sight, ready to respond. The results were swift: police reported the first incident occurring in under 10 minutes. Over the roughly month-long operation, it led to 18 arrests for offences including harassment, sexual assault, and theft. What struck a chord with so many was how quickly it happened. For women who’ve long described this reality, the operation proved the problem wasn’t rare, exaggerated, or “all in their heads.” Police were simply testing the reports — and the evidence came almost immediately. The initiative, named Jog On, was launched after local surveys revealed widespread experiences of harassment among women runners, with nearly half saying they had never reported it. Sources: Surrey Police, The Guardian, LBC, The Sun What do you think — are undercover operations like this one of the most effective ways to tackle street harassment?
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First thing come to your mind when you see this? 🤔
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🌊 A World With No Land — Only Endless Ocean 🌌 Imagine a planet bigger than Earth, completely covered in water. No continents. No islands. No shorelines. Just a vast, deep global ocean wrapping from pole to pole — deeper than anything we have on Earth. This isn’t science fiction. It’s TOI-1452 b, a real exoplanet discovered about 100 light-years away. Scientists believe it could be an “ocean world,” with water potentially making up a huge percentage of its mass. Models suggest an immense liquid ocean, possibly tens to hundreds of kilometers deep, sitting atop a rocky core and high-pressure ice layers below. 🔭 Discovered by NASA’s TESS mission and confirmed by researchers at Université de Montréal, it’s one of the most promising candidates for a water-dominated planet ever found. The big question: If a planet has no land at all… what kind of life could evolve there? Would it be microbial mats and chemosynthetic ecosystems around deep-sea vents? Or could complex, intelligent beings rise — creatures that swim through an endless blue world, never touching solid ground? In a universe this vast, Earth’s mix of land and sea might be the exception, not the rule. What do you think life on such a world would look like? Could humanity ever visit — or even live on — a planet like this? Sources: NASA / Université de Montréal / The Astronomical Journal #TOI1452b #OceanWorld #Exoplanets #Astrobiology #Space
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At 108 years old, Susan Young Browne did something many people never think twice about. She renewed her driver's license. The renewal, issued in Delaware, is valid until 2033—meaning she has been cleared to keep driving until the age of 115. And she's not keeping it as a souvenir. Susan still drives herself three times a week to her local activity center, where she joins group exercise classes and is greeted with cheers from friends each time she arrives. Her mornings begin the same way they have for the past two decades—with a workout on the floor of her own home. Born in 1918, Susan has lived through more than a century of history. She grew up on a farm during segregation without running water or electricity, later earned a teaching degree, and spent 30 years teaching in a one-room schoolhouse. When retirement finally came, she made a decision. After spending three decades on her feet in the classroom, she wasn't about to stop moving. That mindset has stayed with her ever since. When Susan celebrated her 108th birthday, more than 130 people came to honor her, including the state's governor, who joked that he wanted to learn the secret to such a long and active life. Susan's answer was refreshingly simple. She just tries to grow older gracefully. Her story is a reminder that age doesn't have to define what we're capable of. Sometimes, the secret isn't chasing youth—it's never giving up on living. 💛
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For nearly 20 years, Dr. Jorge Zamora-Quezada was one of the most prominent rheumatologists in South Texas. He ran clinics across McAllen, Brownsville, Mission, and San Antonio, commuting between them in a Maserati GranTurismo and a private jet — both emblazoned with his initials, ZQ. He told his patients they had rheumatoid arthritis. Then he treated them aggressively for it. Out of nearly 100,000 Medicare patients he saw, 72.9% left with an RA diagnosis — more than five times the 13% average of seven other rheumatologists in Texas. Almost none of them actually had the disease. Instead, thousands of people endured years of unnecessary chemotherapy injections, lengthy intravenous infusions, frequent office visits, MRIs, X-rays, and other invasive treatments for a lifelong condition they never had. The side effects were severe. Patients later testified about suffering strokes, hair loss, liver damage, and necrosis of the jawbone. One patient described being kept in bed for so long on so many medications that she “didn’t feel like my life had any meaning.” He even treated children as young as 13. The Department of Justice estimated he submitted over $325 million in fraudulent claims to Medicare, Medicaid, TRICARE, and Blue Cross Blue Shield, of which roughly $118 million was paid. Former employees said he enforced strict quotas for procedures and once threw a paperweight at a staff member who failed to meet them. He reportedly preferred hiring doctors on J-1 visas because their immigration status gave him more control. He referred to himself as “la eminencia” — the eminence. When federal investigators served him with a grand jury subpoena, he began ordering ultrasounds on his own employees and using those images to fabricate documentation in patient files. On May 21, 2025, a federal judge sentenced the 68-year-old doctor to 10 years in prison. He forfeited his Maserati, his private jet, 13 luxury properties across Aspen, San Diego, Puerto Vallarta and other locations, and $28 million in cash. The Justice Department described it as one of the most significant cases of patient harm seen in a decade.
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Which is the ideal male body? 😏
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