Blue Ghost Makes a Historic Landing on the Moon

Firefly Aerospace's Blue Ghost lunar lander has made its mark on the Moon, landing successfully on March 2, 2025. This marks Firefly's first Moon landing and CLPS delivery, as part of NASA’s Artemis campaign. The lander brought along 10 NASA science and technology instruments that will explore the lunar surface for about 14 Earth days. This achievement highlights a significant step in commercial space exploration under NASA’s Commercial Lunar Payload Services initiative.

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Why John Tesh Credits His Wife for Saving His Life Amid His Cancer Battle

John Tesh says he shouldn’t even be alive. But at 73, the composer and former TV host is not only surviving — he’s thriving, thanks in large part to his wife, Connie Sellecca. In an exclusive interview with PEOPLE, Tesh opened up about his years-long battle with prostate cancer and the moment everything changed: when Connie stepped in. Diagnosed with stage III prostate cancer in 2015, Tesh was initially told his tumors might be inoperable. Doctors warned he could have just 18 months to live. “I was in the heat of it,” he said. “And Connie mentioned two friends who might be able to help.” Those friends, whom she’d met more than five decades earlier during her modeling days in New York, pointed them to MD Anderson Cancer Center in Houston. “They said, ‘You gotta come here,’” Tesh recalled. And that advice may have saved his life. Unlike other hospitals that had treated fewer than 100 similar cases, MD Anderson had managed over 1,000. “They had more experience,” Tesh said. “They treat the whole body, not just the cancer.” That shift in care came after an MRI in 2017 revealed the cancer had spread to his pelvic lymph nodes, two years after what he thought had been a successful radical prostatectomy. Tesh now continues to monitor the disease with his team at MD Anderson, and recently spoke at a fundraiser for the hospital. “I feel I owe my life to them,” he said. His cancer journey isn’t the only thing making a comeback. Tesh is also enjoying renewed attention for Roundball Rock, the iconic NBA on NBC theme he composed in 1990. NBC recently revived the song for upcoming 2025 broadcasts. Tesh had recorded a new orchestral version — but fans overwhelmingly asked for the original. “They said, ‘No, no, no, we want the OG version,’” he said. “So the version you’re hearing now is the demo I did in 1999.” The resurgence mirrors his own. “There’s definitely an analogy there,” he said. “Both the song and I are rising from the ashes.” Tesh also released The Sports Album, a collection of high-energy sports themes, and says he’s feeling more grounded these days — thanks to music, family, and time with his three grandchildren. “I shouldn’t even be alive now,” he said. “I’m really grateful. This is a great place right now — this minute — to be grateful.”

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How This Teen Inspired Millions With Her Journey From Paralysis To TikTok Fame

At 16, Emma Traveller’s world changed in an instant. A spontaneous double date to the sand dunes turned into a life-altering accident when the UTV she was riding in rolled four times. She hit her head on the roll cage and woke up paralyzed, unable to feel or move anything. Doctors told her she’d broken her neck — C5 through C7 — and suffered spinal cord damage at C4. She couldn’t breathe on her own, eat, or even cough. “I thought my life was over,” she says. “One day I was a healthy teenager — the next, I couldn’t even breathe on my own.” That moment marked the beginning of a journey that would ultimately lead her to build a community of more than 600,000 people on TikTok. Traveller spent 10 days in intensive care before transferring to Craig Hospital in Colorado, a leading spinal cord rehab facility. There, she began the painstaking process of learning how to live again — breathing without machines, swallowing, sitting up, slowly regaining movement in one arm. Her first breakthrough came with something small but symbolic: drinking from a straw. It was slow. It was frustrating. And it was deeply emotional. “There were mornings I didn’t want to get out of bed,” she says. “But then I reminded myself: I have a wheelchair. I’m alive. I chose gratitude, and that choice kept me moving forward.” While recovering, she started looking online for others like her. That’s when she discovered Makayla Noble, a former cheerleader who became a quadriplegic after an accident. Noble’s story lit a spark — and gave her permission to tell her own. Traveller, now 20, began documenting her life on TikTok and Instagram. She shared everything: daily routines, workout attempts, frustrations, small wins. Her openness resonated. Messages began pouring in from people going through their own struggles. “My family was recently in a Razor accident… I am so encouraged by your story and your attitude!” one person wrote. Another, a paraplegic of three years, said, “I’m still trying to be grateful I’m alive, but sometimes it’s hard.” Others thanked her for simply being real. “I love it when people going through really hard things message me to say my page helped them get through it,” she says. “It makes me want to keep doing this forever.” Today, she’s turned that momentum into purpose. Traveller now travels to speak at schools and conferences, visits kids in hospitals, and is writing a book with her mom. She also interned with an adaptive fashion designer in New York — inspired by the challenges she faced getting dressed after her injury. When she’s not working on speeches or therapy, she fills her days with movement and connection. “Getting ready takes longer, so I have to wake up early — but it’s worth it,” she says. “Staying busy keeps me out of my head and connected to everyone else.” Through it all, her message is clear: being in a wheelchair doesn’t mean giving up on happiness. It just means learning a new way to live. “I didn’t get the outcome I wanted — I wanted to go back to cheer and be my old self — but I’ve learned how to live in this new way,” she says. “Your circumstances don’t determine your happiness.” Traveller is quick to point out that life before the accident wasn’t perfect, either. “I used to constantly compare myself to others and struggled with body dysmorphia,” she says. “Now, I feel more confident because I focus on gratitude.” To others going through hardship, she offers the same advice she gives her younger self: “Stop comparing. Be kind. Everyone faces challenges — illness, mental health, family stuff. Helping others helps you, too.” What began as tragedy has turned into impact. And for Emma Traveller, that impact has become a calling.

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Art Gallery Of Ontario Receives 450 Iconic Works From Warhol, Lichtenstein

The Art Gallery of Ontario is receiving a transformative gift — more than 450 artworks spanning over six decades of collecting — from the late Toronto philanthropists Morton and Carol Rapp. The donation, which comes from the couple’s estates, features works by some of the most significant names in postwar and contemporary art. It includes 13 screen prints by Andy Warhol, among them four portraits of Marilyn Monroe from 1967, and early works by David Hockney and Roy Lichtenstein. Also included are nine pieces by Jasper Johns, seven by Claes Oldenburg, and a selection of works by Robert Rauschenberg, including a screen-printed sculpture and an illustrated book. The AGO described the donation as a “significant bolstering” of its Prints and Drawings Collection, especially in capturing the explosion of printmaking that defined the late 1960s and 1970s. “This gift… enables [the AGO] to tell the full story of the medium’s renaissance in the late 1960s and 1970s and its ongoing evolution throughout the early decades of the 21st century,” the museum said in a statement. The donation also marks the AGO’s first acquisition of work by Abstract Expressionist Barnett Newman, whose 1964 lithograph CANTO XVIII is now entering the collection. The Rapps began collecting prints in the 1960s, drawn to the bold colours and experimental forms of the Pop art movement. In the 1990s, they shifted focus to photography, acquiring a chromogenic print by Yinka Shonibare and five photogravures by Kara Walker — all of which are now part of the AGO’s holdings thanks to the gift. “More than collectors, Carol and Morton Rapp were stewards of great art, eager to share and preserve the things that brought them pleasure, beauty, and insight,” said Stephan Jost, the AGO’s director and CEO. “During their lifetimes they contributed immensely to the cultural fabric of Toronto and to the AGO, and this gift by their family is a heartfelt expression of their enduring commitment to this place.” The couple’s relationship with the AGO stretches back to 1966. Over the decades, they donated 474 works, and this latest gift brings their total contribution to nearly 1,000. Carol Rapp, who passed away in 2023, was an actress and singer. Her husband, Morton, died in 2024. He was the former president of Smith Belting, which he expanded into the Canada-wide Multipower brand. The two were married for over 71 years. Their son-in-law, Jay Smith, continues their connection to the museum as a trustee. The donation comes as the AGO undergoes a major expansion. With designs by Diamond Schmitt, Selldorf Architects, and Two Row Architect, the museum is adding 40,000 square feet of gallery space, funded by a $35 million gift from Dani Reiss, chairman and CEO of Canada Goose. The project will add 13 new galleries across five floors, according to the AGO’s website. The Rapp gift ensures those new spaces will be filled with a deeper, more comprehensive collection — one that captures not just the art of the last century, but the passion of two lifelong collectors who never stopped sharing what they loved.

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Habitat Horticulture Transforms Graffiti-Prone Walls Into Lush Pollinator Gardens

In a cityscape dominated by chain-link fences and graffiti-tagged walls, a California company is offering a striking alternative: living meadows that grow vertically. Habitat Horticulture, a firm based in Berkeley, has launched a project that replaces blank, graffiti-prone surfaces with panels of wildflowers and native grasses. Their creation, called Meadowall, is a pre-seeded, modular system that turns ordinary fences and walls into lush, colorful corridors for pollinators and pedestrians alike. The idea took root right in their own backyard. “Just down the street from Habitat Horticulture’s headquarters, a newly built fence along the greenway bike path was quickly covered in graffiti,” the company shared in a statement. Instead of repainting or ignoring it, the team saw an opportunity. They installed Meadowall panels over 1,500 square feet of fence near their Berkeley offices. Within weeks, the once-bland surface had sprouted into a living meadow. “As it grows, it transforms an ordinary walkway into a vertical meadow,” the company posted in a video. “A vital connection to nature for people and pollinators alike.” The change was more than visual. The installation created real habitat for birds, butterflies, and native bees, while also reducing urban noise and filtering dust and air pollution. According to the company, the panels lower sound pollution by an average of 15 decibels and trap harmful particulate matter from nearby traffic. “What was once a target for graffiti is now a vibrant, dynamic landscape,” the team wrote on their website. “It demonstrates how even the most utilitarian surfaces can become ecological assets.” The system is cost-effective, too. By using seeds rather than mature plants, Meadowall costs about 30 percent less to install and requires minimal maintenance. That balance of sustainability and practicality has led to growing demand in both indoor and outdoor spaces. In addition to outdoor walkways and fences, the panels have been installed in office lobbies, apartment buildings, college campuses, and even the side of a high-rise in San Francisco’s Tenderloin neighborhood. That Tenderloin project has become a centerpiece of urban design in the area. “Straddling the corner of the building, the wall appears almost like a sentient being,” the company wrote, “contrasting the angular architecture with lush, soft plantings.” Beyond aesthetics, it helps restore green space in one of the city's densest neighborhoods. For Habitat Horticulture, the mission is part public art, part environmental commitment. “Easy to install and maintain, Meadowall offers a sustainable, visually stunning way to enhance urban spaces, communicate environmental commitment, and deter graffiti,” they say. In short: the next time you see a wall full of spray paint, imagine it blooming instead.

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Sister Act of Kindness: Whoopi Goldberg Spreads Cheer by Answering Santa Letters for Children

Whoopi Goldberg has a holiday tradition that comes straight from the heart — answering letters to Santa. The 70-year-old actress and The View co-host shared on the Behind the Table podcast that each Christmas, she quietly takes time to respond to letters kids send to Santa Claus through the U.S. Postal Service. “I just feel like everybody needs a little help, and if you can help somebody... it's why I try to do Santa at the post office,” Goldberg said. “I try to get letters and we try to answer kids' letters to Santa.” “It’s things that we can do, and it doesn’t cost a lot,” she added. “Because you want to give people the ability to do something that brings up how they see themselves.” The small but thoughtful gesture is one of the ways Goldberg gives back during the holiday season — and it’s something she’s been doing for years. The comments came during a special podcast episode celebrating her 70th birthday, which also aired as a tribute on The View. The show highlighted several of Goldberg’s favorite charities, including One Simple Wish, which supports foster children; The Heifer Project International, which combats hunger through livestock donations; and God's Love We Deliver, which provides meals to people affected by serious illness, including HIV/AIDS. Goldberg said supporting those in need is more important now than ever. “A lot of people aren’t getting what they need,” she said, pointing to rising costs of living and financial insecurity. “It’s not fair. People used to actually have savings. And people can’t hold onto their savings, because every time you turn around, somebody’s hand is out.” Even with her own milestone birthday underway, Goldberg kept the focus on others. She marked the occasion on-air with her co-hosts — all except Joy Behar, who missed her third show in a row due to a broken toe. Behar still found a way to celebrate, sending Goldberg a birthday lasagna instead. As Goldberg put it, giving doesn’t always have to be big to be meaningful. A handwritten letter can go a long way.

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Quarterback Finishes Final College Football Game After Cancer Diagnosis

Four early morning drives down US Route 52 shaped the most unlikely season of football in Minnesota this year. They started around 4 or 5 a.m. and always headed toward Rochester. Four Mondays. Four one hour rides. Three different drivers. One mission. Help Jack Curtis keep playing the game he loves. Curtis is a senior quarterback at Carleton College. He also has Stage 2 Hodgkin’s lymphoma. Anyone else in his situation would step away from the field. Doctors at the Mayo Clinic told him they knew of no college football player competing during treatment. His athletic trainer spent 16 years in the NFL and has never seen it. Chemotherapy drains strength, clouds thinking, and leaves most people stuck in bed. Curtis planned to suit up anyway. Every other Monday this fall, starting on September 8, he arrived at the Mayo Clinic for long days of tests, blood work and chemotherapy. The medication flowed through a port in his chest. By the time he left, 12 hours had passed. Early Tuesday morning, he returned for an immunotherapy shot timed precisely 19 hours after the final infusion. By Wednesday, the protective effects of his anti-nausea medication wore off and he could not leave his bed. By Thursday afternoon, he shuffled to the practice field with a lawn chair. Fridays were a little better. He sometimes threw a few passes during a walk through. And on Saturdays, he played college football. Curtis has thrown for 2,776 yards and 26 touchdowns this season. He broke two school records and ranks near the top nationally in several Division III categories. Carleton is 6 to 3 with him at quarterback. “I do not know what the word to use is,” his father, Scott Curtis, said. “Awe, I guess. Yeah. I think it is awe.” Football has been central to Curtis’ life since childhood. He grew up in Charlotte in an athletic household. His father played football and tennis. His mother, Amy, played lacrosse and field hockey. As a kid, Curtis ran the Air Raid offense in Pop Warner games. He played both sides of the ball and laughed about how he earned the nickname “Spiderman.” “I’d get run over but I’d hold onto the other guy’s jersey for dear life and drag him down,” he said. He kept that attitude through injuries, setbacks and the stressful college recruiting years. He eventually landed at Carleton, a small school far from home. It was not his first choice, but the fit turned out to be right. He became the starter as a sophomore and built a close circle of teammates who became his roommates. They cook dinners together, play Mario Kart and plan for life after graduation. Curtis hopes to pursue aerospace engineering. Cancer arrived in the middle of all of it. He felt the first lumps in the spring. They did not hurt, so he ignored them. By summer, a mass sat under his arm and the pain spread across his chest. One night he woke up with an intense stabbing sensation. He wrote letters to his parents, his girlfriend and his best friends. “I thought about life without Jack Curtis in it,” he said. Two weeks of tests brought no answers until a biopsy in Charlotte confirmed Hodgkin’s disease. The cancer had spread in his chest cavity and surrounded his heart. Curtis cried until his doctor told him it was treatable. Then he asked if he could delay treatment until after football season. “The doctors laughed at us,” Amy said. “They said, ‘We’re starting next week.’” Treatment hit him hard. He spiraled through questions about school and football and the future. But after his second round of chemo, a PET scan showed no active lymphoma cells. The cancer was not gone, but he was making progress. He burned the letters he had written on the worst night of his life. Curtis asked his doctors if he could return to Carleton and continue treatment at the Mayo Clinic. Then he asked the bigger question. Could he play? “Well,” his doctor said, “it’s not like football is going to give you more cancer.” That answer opened a door that required perfect timing and massive logistical work. Treatments had to stay exactly on schedule. Immunotherapy had to happen on Tuesday morning. The medical teams coordinated records and insurance paperwork so Curtis could focus on school and football. His parents had to decide how to support him from 1,100 miles away. Amy wanted to keep him home but knew he needed to live his life. “Denying him was not an option,” she said. Carleton’s staff took over once he returned. Head coach Tom Journell personally drove him to his first Mayo appointment. “I was like, ‘You’re going to what now?’” Journell said when Curtis told him he intended to play. Trainers tracked his hydration and monitored his nutrition. Teammates cooked meals, drove him to appointments and guarded his privacy until he chose to share his story. Curtis delivered on the field. In his second game, he threw for 478 yards and six touchdowns. Some weeks he could barely move by Thursday, but on Saturdays he found a way to perform. “You look at him and think, ‘No way,’” athletic trainer Ron Roche said. “And then he goes out there on Saturday and zings the ball around.” The season has not been perfect. He injured the index finger on his throwing hand late in the year. Against Bethel, he pulled himself out because he could not grip the ball. Carleton lost. Roche made a custom splint to give him a chance for the finale. “I would never count him out,” he said. Curtis faces radiation next. He returns to the Mayo Clinic on November 19 to map out his schedule. Starting December 1, he will go back every day for treatment. If all goes well, he will ring the bell on December 19. He does not pretend any of this has been easy. But he knows why he kept going. He wanted the ordinary things. The games with his roommates. The team dinners. The feeling of being part of something that existed long before cancer and will exist long after it. Before each game, Curtis walks to the 50 yard line, drops to his knees and flicks a football toward the end zone. He used to hit the crossbar from that distance during a family trick he practiced with his dad. Now it falls short. “I can get it there,” he said. “And that was good enough.”

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Arizona Rescue Team Airlifts Injured 57-Year-Old Hiker to Safety

A hiker was airlifted to safety after breaking her ankle on a mountain trail near Superior, Arizona, on the afternoon of November 14. The Pinal County Sheriff’s Office (PCSO) said their search and rescue team got a call about the 57-year-old hiker at approximately 1:30 pm, and were informed of her injury. Border Patrol Search, Trauma, and Rescue (BORSTAR) paramedics and PCSO search and rescue teams located the woman and treated her for her injuries before a helicopter hoisted her to safety. The sheriff’s office said the woman was taken to hospital in a stable condition.

A Lost Bach Piece Was Just Performed For the First Time In 320 Years

Two previously unknown organ pieces by Johann Sebastian Bach have been performed in Germany after more than three centuries. Germany's Culture Minister Wolfram Weimer described the discovery of these works as a "great moment for the world of music." The journey to this revelation started in 1992 when Peter Wollny, a noted researcher of the celebrated German composer, came across these manuscripts while cataloguing Bach's works at the Royal Library of Belgium in Brussels. The compositions, Chaconne in D minor BWV 1178 and Chaconne in G minor BWV 1179, were initially undated and unsigned. Wollny devoted three decades to confirming their authenticity. These pieces graced the air at St Thomas Church in Leipzig, where Bach himself is buried and where he served as cantor for 27 years. Dutch organist Ton Koopman had the honor of performing them, marking their first public performance in 320 years. Koopman expressed his pride, noting that the pieces are "of a very high quality" and suitable for smaller organs as well. Believed to be composed early in Bach's career during his time as an organ teacher in Arnstadt, Thuringia, these works add a significant chapter to our understanding of his early development. Wollny, now director of the Bach Archive in Leipzig, highlighted distinctive characteristics within these compositions that align with Bach's style from that period. He stated that certain stylistic features present are exclusive to Bach’s work. It's believed Salomon Günther John, one of Bach’s pupils, documented these pieces back in 1705. During the presentation event for these works, Wollny expressed strong confidence—99.99 percent sure—that they belonged to Bach. These newly attributed compositions are now officially part of the catalogue of Bach’s works. This discovery not only enriches what we know about Bach but also offers fresh material for musicians today. The addition of these pieces provides new opportunities for interpretation and performance within classical music circles.

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Life-Changing Surgery Allows Boy With Rare Condition To Experience First Sleepover

Seven-year-old William from Bath, England, is experiencing new adventures thanks to a significant surgery that has transformed his life. Born with Treacher Collins syndrome, a rare genetic condition affecting skull and facial bone growth, William faced challenges with breathing, eating, and swallowing. In May, surgeons at Bristol Children's Hospital gave him an eight-hour operation that rebuilt his jaw using bone grafts taken from his ribs. This procedure allowed him to breathe and eat on his own for the first time. Now, as he looks forward to turning eight, he can enjoy activities most kids take for granted. William’s mother, Kate, shared with BBC Radio Bristol how severe her son’s condition was from birth. "From birth he struggled to breathe and was given a tracheostomy at two weeks old," she explained. A tracheostomy involves creating an opening in the neck where a tube is inserted to assist breathing. This meant William needed someone constantly by his side who knew emergency procedures if he stopped breathing. The recent surgery has changed everything for William. Surgeons removed the tracheostomy tube and used part of his rib bone to create new jaw joints. "A frame was put into his lower jaw and we were turning these screws to try and artificially pull it forwards," said Kate about the complex procedure. With this medical breakthrough behind him, William no longer requires constant supervision by someone trained in managing emergency airway issues. Now he's eager to experience things like water slides, sleepovers, and play dates—activities many children cherish but were previously out of reach for him. "He's desperate to go down water slides and he's lined up his little besties to have sleepovers and to go on play dates," Kate shared enthusiastically. She also admitted that when William finally has his first sleepover, she probably won't sleep at all due to excitement.

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Giraffe Undergoes Successful Surgery For Rare Knee Condition

Vets at Woburn Safari Park in Bedfordshire, England, successfully completed high-risk surgery on one of their tallest residents, Sahara the Nubian giraffe. Weighing in at 500 kilograms, Sahara had been suffering from a rare knee condition known as "locking stifle," which severely limited her mobility by causing her leg to lock. Nathalie Wissink-Argilaga, the head vet at the park, described it as one of the most complex cases they've ever tackled. Due to the lack of precedent in giraffes, the veterinary team decided to adapt an equine technique to stabilize Sahara's joint. This innovative approach marked a significant step forward in treating giraffes with similar conditions. The operation wasn't straightforward. The unique anatomy of such a large animal made anesthesia particularly unpredictable. Lying down for too long could also pose risks like compromised blood circulation and other life-threatening complications. To tackle these challenges, the team prepared a deep hay bed and supported Sahara's neck with a wooden board during the procedure. They used blindfolds and earplugs to keep her calm while keepers massaged her neck to maintain circulation. The specialist team included not just vets but also an equine surgeon and an anaesthetist. Their combined expertise paid off when Sahara was quickly back on her feet after the one-hour procedure. "Following her surgery, Sahara was quickly back on her feet - a moment of joy for the dedicated veterinary and keeper teams who supported her throughout," noted Woburn Safari Park in a statement. Sahara's recovery is progressing well under careful monitoring of her movement and behavior. Thanks to this successful operation, she has returned to her familiar self with renewed confidence.

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