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Tag: Children's books

  • NBCDI’s BTM Awards recognize groundbreaking creators in Black children’s books, toys, and media

     The National Black Child Development Institute (NBCDI) is set to host the inaugural Book, Toy, & Media (BTM) Awards on Saturday, October 25, 2025, at The Dogwood in Atlanta, GA. This landmark event will celebrate the power of Black creativity in shaping the imaginations, identities, and futures of Black children everywhere. 

    Hosted as part of NBCDI’s 2025 National Conference, the evening will feature Jason Reynolds, #1 New York Times bestselling author, as keynote speaker. It will also honor groundbreaking BTM Champion Awardees whose work has transformed the landscape of culturally affirming children’s content: 

    U.S. Senator Reverend Raphael G. Warnock 

    Dr. Lisa Williams 

    Jacqueline Woodson 

    Ralph Farquhar 

    Bruce W. Smith 

    Makeda Mays Green 

    Honoring Visionaries: Award Recipients Across Five Categories 

    In addition to the Champion Awards, NBCDI will recognize creators whose visionary books, toys, and media are setting a new standard of excellence for Black children: 

    ● First Light Book Award (ages 0 – 3): Cedella Marley (Author, Is This Love?) 

    ● Infinite Possibilities Book Award (ages 4 – 8): Jamilah Thompkins-Bigelow(Author, Your Name is a Song) 

    ● First Light Toy Award (ages 0 – 3): Tyshia Ingram (inventor, ABC Affirmation Flash Cards-Black Boy Joy) 

    ● Infinite Possibilities Toy Award (ages 4 – 8): Zoe Oli (inventor, Curly + Confident Clubhouse) 

    ● Kuumba Media Excellence Award (ages 2 – 8): Fracaswell “Cas” Hyman (creator, writer, director, and producer, Bookmarks) 

    A Rigorous and Trusted Process 

    Winners were selected through a careful, community-rooted process shaped by the BTM Awards Advisory Council — including Eileen Robinson, Claire Green, Ehi Oviasu-Kahn, and Lola Rooney — and finalized by the BTM Awards Review Board, featuring Tatjyana Elmore, Ed Greene, Diane Jones-Lowrey, James Howard, Heather Jenkins, and Terri-Nichelle Bradley. 

    A Collective Movement for Representation 

    The BTM Awards are made possible by partnerships and collaborations with leaders across publishing, toys, and media, including the Children’s Book Council, Common Sense Media, Astra, Women in Toys, and The Toy Foundation. 

    The event is sponsored by visionary supporters including Disney Entertainment, Bainum Family Foundation, Penguin Young Readers, and Random House Children’s Books. In-kind sponsors include Simon & Schuster, Random House Children’s Books, Penguin Young Readers, and more. 

    A Future Where Every Black Child Is Seen 

    “The BTM Awards are more than a celebration — they are a declaration,” said Dr. Leah Austin, President & CEO of NBCDI. “Black children deserve books, toys, and media that reflect not only who they are but who they are becoming. This is about shaping futures and ensuring joy, imagination, and innovation remain central to their growth.” 

    Tickets for the Book, Toy, & Media Awards are available through NBCDI’s Conference Registration portal: www.nbcdi.org/conference25 

    Staff Report

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  • The Joys of Moomscrolling


    For this week’s Fault Lines column, Jon Allsop is filling in for Jay Caspian Kang.


    If you were to drop by my apartment, you’d see a lot of Moomins. My girlfriend and I own all sorts of trinkets bearing their likeness: a selection of mugs, a teapot, a tea towel (that we framed and put on the wall), a bedside night light, a pair of light-up key rings, a necklace, a wallet, a plastic model from a vending machine in Japan, at least one Christmas-tree decoration, a poster, and a pair of fridge magnets that, in the absence of a magnetic fridge door, we’ve posed on either side of our fireplace. They look like heraldic bas-reliefs.

    What are Moomins, you might be wondering. They’re children’s characters, dreamed up decades ago by the Finnish writer and artist Tove Jansson, that are white and rotund, with pointy ears, swishy tails, and rounded snouts; they’re sometimes likened to hippos, which is fair, even if the comparison doesn’t particularly resonate with me. (To me, they just look like Moomins, a fact that is partly because I’ve been familiar with them since my early childhood, but is also a reflection of their singular visual identity; as Sheila Heti once put it in this magazine, they are “strangely familiar, as though Jansson happened to look in a new direction and find these tender and serious fellow-creatures, who had been with us all along.”) Then again, you might not be wondering what Moomins are—they have fans all over the world, and my girlfriend and I are far from alone in having stuffed our home with their merchandise, worldwide sales of which reportedly top eight hundred million dollars per year. (The Moomin mugs, each wrapped in a gorgeous illustration, are the jewels in this crown, and are highly collectible; in 2021, one sold at auction for nearly thirty thousand dollars.) Other fans include the actor Lily Collins, a.k.a. Emily of “in Paris” fame, who not only collects the merchandise but named her daughter Tove and hosted the introductory episode of an official Moomin podcast.

    On the podcast, which premièred in the spring of 2023, Collins said that, when she first started collecting Moomin paraphernalia, it was “impossible” to find in the U.S. This has changed in recent years: alongside the podcast launch, Moomin Characters (the company that manages the rights to Jansson’s creations) and Barnes & Noble announced “a significant new partnership to make Jansson’s literature widely accessible to American audiences, both in stores and online” (including, yes, a plan to sell mugs); since then, there have been collaborations with Urban Outfitters and luxury labels including Rei Kawakubo’s Comme des Garçons. This year, which marks the eightieth anniversary of the Moomins’ début, there have been further signs of a Finnish invasion, including an ongoing exhibition at the Brooklyn Public Library—the first ever dedicated to Jansson in the U.S.—which reflects Jansson’s progressive values. She was a committed pacifist and antifascist, and, early in her career, she worked as a political cartoonist, poking fun at dictators; Linda E. Johnson, the president and C.E.O. of the Brooklyn Public Library, has noted that Jansson was also openly queer, at a time when being gay was criminalized in Finland, and that the decision to highlight her work was timed to coincide with Pride Month. “It speaks to what’s going on culturally,” Johnson said, “and lets our audience know: The Brooklyn Public Library is not backing down.” The exhibition is titled “The Door Is Always Open.” (Earlier in the summer, a Moomin public art work in London, produced in partnership with an initiative celebrating refugees, bore the same moniker.)

    An executive at Moomin Characters told the New York Times recently that Jansson’s creations “are being discovered in the U.S. by new generations, spreading word from person to person.” Of course, much of this word-spreading is happening on social media. There have long been dedicated Moomin communities on Facebook and Tumblr. The Times reported that Gen Z is intensifying the trend—posting about the Moomins on TikTok, finding old animations on YouTube (that are closer to Jansson’s drawings than more modern 3-D offerings), and, in the process, ushering the Moomins into “a global pantheon of cuteness.” This cuteness is, surely, a key driver of the Moomins’ online appeal, as is the sense that the characters have an “inherent gentle wonderment”—as one writer recently put it after visiting the Brooklyn exhibition—that offers an escape from the many anxieties of modern life. The Moomins’ association with escapism is not a new thing: Jansson once wrote that she created them when she “wanted to get away from my gloomy thoughts” and enter “an unbelievable world where everything was natural and benign—and possible.” When, in the nineteen-fifties, a London newspaper that commissioned a Moomin comic strip stipulated there be no politics, sex, or death, Jansson is said to have replied that she didn’t know anything about the government, that the Moomins can’t anatomically have sex, and that she once killed a hedgehog, but nothing else.

    And yet the books that Jansson wrote about the Moomins contain, sometimes explicitly and other times by way of metaphor, political themes—war, displacement, imminent annihilation, environmental catastrophe—that hardly serve as distractions from the many dangers of the world, then or now. Earlier this year, the author Frances Wilson wrote, in a New Statesman essay about the “dark side” of the Moomins, that “one of the oddest aspects of the Moomin phenomenon is how these complex tales of apocalypse, breakdown and disfunction have been consistently misread as cutesy celebrations of domestic life.”

    Time to box up the mugs, then? Not exactly. While some of the Moomins’ newer online fans might be ignorant of the angst—not to mention weirdness—of Jansson’s œuvre, I don’t see any incompatibility between her cute illustrations and the ambient existential dread that pervades their adventures. If anything, this juxtaposition makes the Moomins perfect guides through our muddled moment, online and off. Ultimately, we could all usefully spend a little less time doomscrolling, and a little more time Moomscrolling.

    Technically, it isn’t quite right to say that this year marks the eightieth anniversary of the Moomins’ début. Jansson first drew a Moomin-like creature (intending it to be ugly, not cute) when she was a child, sketching it onto an outhouse wall following an argument with her brother about the merits of Immanuel Kant; later, her uncle would caution her against raiding the cupboards for a midnight snack by warning that, if she did, the “Moomintrolls” that live behind the stove would press their cold snouts against her legs. At some point after Jansson started contributing satirical cartoons to Garm, a Finnish magazine, she began drawing a character resembling a Moomin as part of her signature. In one cover illustration, it can be seen peering out from behind the “M” of “GARM.” A caricature of Adolf Hitler is perched on the “G.”

    During the Winter War—which began when the Soviet Union invaded Finland in November, 1939, and would go on to drive hundreds of thousands of Finns from their homes—Jansson started work on what would become the first Moomin book, known today as “The Moomins and the Great Flood,” though it wouldn’t be published until 1945. War was the reality from which Jansson would later say she wanted to escape, but as Heti noted in her review of a pair of works about Jansson, the “Great Flood” is “fascinating for how un-escapist it seems.” The book begins deep in a forest, where a young character named Moomintroll and his mother are searching for “a snug, warm place where they could build a house to crawl into when winter came.” Their subsequent adventures have a dreamlike quality, with each salvation (coming across a garden of lemonade and candy, for example) quickly giving way to a fresh peril (tummyache, in the case of the candy). The gravest danger comes from the titular flood, which drives people from their homes; it would be presentist to read this as a parable for the climate crisis, but it clearly resonates as such. And the illustrations have yet to take on the vibrant, rounded aesthetic that defines the modern Moomin brand. The characters’ snouts are more pronounced. Clean lines sometimes dissolve into washes of dark ink.

    The “Great Flood” has often been considered apart from the subsequent Moomin canon: Jansson later referred to it as “a banal story without any personality”; it was translated into English only in 2005, after she died. But similar themes run through the later books. “Comet in Moominland” (1946) can be read as an allegory for the fear of nuclear apocalypse (a resonance that must have eluded me when I read the novel as a child, realizing it only years later during a trip to an exhibit at the Moomin museum in the Finnish city of Tampere). Wilson describes the sixth Moomin book, “Moominland Midwinter,” as containing “the most devastating account of depression in 20th-century literature,” and notes that, in a later comic strip, a psychiatrist puts Moomintroll on meds that shrink him out of existence. The last of Jansson’s Moomin novels, “Moominvalley in November,” sees the Moomin family go missing, and a variety of side characters reflect on their elusiveness. Wilson and others have likened it to “Waiting for Godot.”

    This is not to say that the Moomin books are depressing. Some of them have overtly happy endings: the flood leads to a new home for the Moomin family; the comet misses. And they are funny, able to find levity in impending disaster. (When one character defines the word “catastrophe,” another counters that it is, “in other words—‘fuss.’ ”) Over all, my abiding memory of the books is that they are full of life, despite the world’s complications. “It would be awful if the earth exploded,” a different character says, in “Comet.” “It’s so beautiful.” This philosophy, I think, is what keeps the Moomins in my heart (and my home). If the underlying themes can be anxiety-provoking, then the Moomins themselves are anchoring presences—whatever may happen to the world, and whether or not we can control it.

    Jon Allsop

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  • Children’s Author Says ‘Pay What You Can’ for His Bestselling Diverse Books for Kids

    Children’s Author Says ‘Pay What You Can’ for His Bestselling Diverse Books for Kids

    Today, bestselling author Bobby Basil announced parents can buy his three diverse book series for kids — Pedro & PeteTexting with History, and Travel Bug — for the price they can afford at bobbybasilbooks.com.

    Pedro & Pete helps kids learn Spanish with interactive activity books and a companion “Spanish to English” podcast, which ranks as a top education podcast for kids in over 20 countries. Texting with History follows text conversations between curious kid Alex and inspiring figures from Black History, Women’s History, and Hispanic Heritage like Frida Kahlo and Harriet Tubman. And interstellar alien Travel Bug explores cultures around the world from Peru down south all the way to Iceland up north.

    Amazon awarded Basil the KDP Select All Star prize as an author who has been read the most on its platform. The Theodore Roosevelt Association recognized him as a national finalist for his book “Texting with Theodore Roosevelt.” And he became another national finalist in Sundance Institute’s New Voices Lab for his virtual reality musical experience for kids.

    Basil realized the hundreds of dollars it would cost to buy all his kids’ books online was more than most families could afford. So he created his own e-commerce store to offer printable ebook versions. Parents pay what they can, and the price starts at a dollar.

    “I want my prices to be as inclusive as the themes in my books,” asserted Basil. “Cost shouldn’t stop parents from teaching their children about diversity. Diversity for kids is priceless.”

    Bobby Basil Books for Kids publishes bestselling read-aloud books that entertain and educate preschool, kindergarten, and elementary school early readers. Basil has also written children’s stories for companies including Disney, Nickelodeon, and Amazon Studios. To learn more about Bobby Basil’s diversity books, visit bobbybasilbooks.com.

    Source: Bobby Basil Books for Kids

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  • In a first, doctors treat fatal genetic disease before birth

    In a first, doctors treat fatal genetic disease before birth

    A toddler is thriving after doctors in the U.S. and Canada used a novel technique to treat her before she was born for a rare genetic disease that caused the deaths of two of her sisters.

    Ayla Bashir, a 16-month-old from Ottawa, Ontario, is the first child treated as fetus for Pompe disease, an inherited and often fatal disorder in which the body fails to make some or all of a crucial protein.

    Today, she’s an active, happy girl who has met her developmental milestones, according to her father, Zahid Bashir and mother, Sobia Qureshi.

    “She’s just a regular little 1½-year-old who keeps us on our toes,” Bashir said. The couple previously lost two daughters, Zara, 2½, and Sara, 8 months, to the disease. A third pregnancy was terminated because of the disorder.

    In a case study published Wednesday in the New England Journal of Medicine, doctors describe an international collaboration during the COVID-19 pandemic that led to the treatment that may have saved Ayla’s life – and expanded the field of potential fetal therapies. The outlook for Ayla is promising but uncertain.

    “It holds a glimmer of hope for being able to treat them in utero instead of waiting until damage is already well-established,” said Dr. Karen Fung-Kee-Fung, a maternal-fetal medicine specialist at The Ottawa Hospital who gave the treatment and delivered Ayla.

    Fung-Kee-Fung was following a new treatment plan developed by Dr. Tippi MacKenzie, a pediatric surgeon and co-director of the Center for Maternal-Fetal Precision Medicine at the University of California, San Francisco, who shared her research after the pandemic prevented Ayla’s mother from traveling for care.

    “We were all motivated to make this happen for this family,” MacKenzie said.

    Doctors have treated fetuses before birth for three decades, often with surgeries to repair birth defects such as spina bifida. And they’ve given blood transfusions to fetuses through the umbilical cord, but not medicines. In this case, the crucial enzymes were delivered through a needle inserted through the mother’s abdomen and guided into a vein in the umbilical cord. Ayla received six biweekly infusions that started at about 24 weeks of gestation.

    “The innovation here wasn’t the drug and it wasn’t accessing the fetal circulation,” said Dr. Pranesh Chakraborty, a metabolic geneticist at Childrens Hospital of Eastern Ontario, who has cared for Ayla’s family for years. “The innovation was treating earlier and treating while still in utero.”

    The unusual partnership also involved experts at Duke University in Durham, N.C., which has led research on Pompe disease, and University of Washington in Seattle.

    Babies with Pompe disease are often treated soon after birth with replacement enzymes to slow devastating effects of the condition, which affects fewer than 1 in 100,000 newborns. It is caused by mutations in a gene that makes an enzyme that breaks down glycogen, or stored sugar, in cells. When that enzyme is reduced or eliminated, glycogen builds up dangerously throughout the body.

    In addition, the most severely affected babies, including Ayla, have an immune condition in which their bodies block the infused enzymes, eventually stopping the therapy from working. The hope is that Ayla’s early treatment will reduce the severity of that immune response.

    Babies with Pompe disease have trouble feeding, muscle weakness, floppiness and, often, grossly enlarged hearts. Untreated, most die from heart or breathing problems in the first year of life.

    In late 2020, Bashir and Qureshi had learned they were expecting Ayla and that prenatal tests showed she, too, had Pompe disease.

    “It was very, very scary,” recalled Qureshi. In addition to the girls who died, the couple have a son, Hamza, 13, and a daughter, Maha, 5, who are not affected.

    Both parents carry a recessive gene for Pompe disease, which means there’s a 1 in 4 chance that a baby will inherit the condition. Bashir said their decision to proceed with additional pregnancies was guided by their Muslim faith.

    “We believe that what will come our way is part of what’s meant or destined for us,” he said. They have no plans for more children, they said.

    Chakraborty had learned of MacKenzie’s early stage trial to test the enzyme therapy and thought early treatment might be a solution for the family.

    The treatment could be “potentially very significant,” said Dr. Brendan Lanpher, a medical geneticist at the Mayo Clinic in Rochester, Minn., who was not involved in the research.

    “This is a progressive disease that builds up over time, so every day a fetus or baby has it, they’re accumulating more of the material that affects muscle cells.”

    Still, it’s too early to know whether the protocol will become accepted treatment, said Dr. Christina Lam, interim medical director of biochemical genetics at the University of Washington and Seattle Children’s Hospital in Seattle.

    “It’s going to take some time to really be able to establish the evidence to definitively show that the outcomes are better,” she said.

    Ayla receives drugs to suppress her immune system and weekly enzyme infusions that take five to six hours — a growing challenge for a wiggly toddler, her mother said. Unless a new treatment emerges, Ayla can expect to continue the infusions for life. She is developing normally — for now. Her parents say every milestone, such as when she started to crawl, is especially precious.

    “It’s surreal. It amazes us every time,” Qureshi said. “We’re so blessed. We’ve been very, very blessed.”

    ———

    The Associated Press Health and Science Department receives support from the Howard Hughes Medical Institute’s Department of Science Education. The AP is solely responsible for all content.

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  • In a first, doctors treat fatal genetic disease before birth

    In a first, doctors treat fatal genetic disease before birth

    A toddler is thriving after doctors in the U.S. and Canada used a novel technique to treat her before she was born for a rare genetic disease that caused the deaths of two of her sisters.

    Ayla Bashir, a 16-month-old from Ottawa, Ontario, is the first child treated as fetus for Pompe disease, an inherited and often fatal disorder in which the body fails to make some or all of a crucial protein.

    Today, she’s an active, happy girl who has met her developmental milestones, according to her father, Zahid Bashir and mother, Sobia Qureshi.

    “She’s just a regular little one-and-a-half year old who keeps us on our toes,” Bashir said. The couple previously lost two daughters, Zara, 2 ½, and Sara, 8 months, to the disease. A third pregnancy was terminated because of the disorder.

    In a case study published Wednesday in the New England Journal of Medicine, doctors describe an international collaboration during the COVID-19 pandemic that led to the treatment that may have saved Ayla’s life – and expanded the field of potential fetal therapies. The outlook for Ayla is promising but uncertain.

    “It holds a glimmer of hope for being able to treat them in utero instead of waiting until damage is already well-established,” said Dr. Karen Fung-Kee-Fung, a maternal-fetal medicine specialist at The Ottawa Hospital who gave the treatment and delivered Ayla.

    Fung-Kee-Fung was following a new treatment plan developed by Dr. Tippi MacKenzie, a pediatric surgeon and co-director of the Center for Maternal-Fetal Precision Medicine at the University of California, San Francisco, who shared her research after the pandemic prevented Ayla’s mother from traveling for care.

    “We were all motivated to make this happen for this family,” MacKenzie said.

    Doctors have treated fetuses before birth for three decades, often with surgeries to repair birth defects such as spina bifida. And they’ve given blood transfusions to fetuses through the umbilical cord, but not medicines. In this case, the crucial enzymes were delivered through a needle inserted through the mother’s abdomen and guided into a vein in the umbilical cord. Ayla received six biweekly infusions that started at about 24 weeks of gestation.

    “The innovation here wasn’t the drug and it wasn’t accessing the fetal circulation,” said Dr. Pranesh Chakraborty, a metabolic geneticist at Childrens Hospital of Eastern Ontario, who has cared for Ayla’s family for years. “The innovation was treating earlier and treating while still in utero.”

    The unusual partnership also involved experts at Duke University in Durham, N.C., which has led research on Pompe disease, and University of Washington in Seattle.

    Babies with Pompe disease are often treated soon after birth with replacement enzymes to slow devastating effects of the condition, which affects fewer than 1 in 100,000 newborns. It is caused by mutations in a gene that makes an enzyme that breaks down glycogen, or stored sugar, in cells. When that enzyme is reduced or eliminated, glycogen builds up dangerously throughout the body.

    In addition, the most severely affected babies, including Ayla, have an immune condition in which their bodies block the infused enzymes, eventually stopping the therapy from working. The hope is that Ayla’s early treatment will reduce the severity of that immune response.

    Babies with Pompe disease have trouble feeding, muscle weakness, floppiness and, often, grossly enlarged hearts. Untreated, most die from heart or breathing problems in the first year of life.

    In late 2020, Bashir and Qureshi had learned they were expecting Ayla and that prenatal tests showed she, too, had Pompe disease.

    “It was very, very scary,” recalled Qureshi. In addition to the girls who died, the couple have a son, Hamza, 13, and a daughter, Maha, 5, who are not affected.

    Both parents carry a recessive gene for Pompe disease, which means there’s a 1 in 4 chance that a baby will inherit the condition. Bashir said their decision to proceed with additional pregnancies was guided by their Muslim faith.

    “We believe that what will come our way is part of what’s meant or destined for us,” he said. They have no plans for more children, they said.

    Chakraborty had learned of MacKenzie’s early stage trial to test the enzyme therapy and thought early treatment might be a solution for the family.

    The treatment could be “potentially very significant,” said Dr. Brendan Lanpher, a medical geneticist at the Mayo Clinic in Rochester, Minn., who was not involved in the research.

    “This is a progressive disease that builds up over time, so every day a fetus or baby has it, they’re accumulating more of the material that affects muscle cells.”

    Still, it’s too early to know whether the protocol will become accepted treatment, said Dr. Christina Lam, interim medical director of biochemical genetics at the University of Washington and Seattle Children’s Hospital in Seattle.

    “It’s going to take some time to really be able to establish the evidence to definitively show that the outcomes are better,” she said.

    Ayla receives drugs to suppress her immune system and weekly enzyme infusions that take five to six hours — a growing challenge for a wiggly toddler, her mother said. Unless a new treatment emerges, Ayla can expect to continue the infusions for life. She is developing normally — for now. Her parents say every milestone, such as when she started to crawl, is especially precious.

    “It’s surreal. It amazes us every time,” Qureshi said. “We’re so blessed. We’ve been very, very blessed.”

    ———

    The Associated Press Health and Science Department receives support from the Howard Hughes Medical Institute’s Department of Science Education. The AP is solely responsible for all content.

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  • The Cloud: The nuclear novel that shaped Germany

    The Cloud: The nuclear novel that shaped Germany

    She sees this legacy reflected in present-day German horror films such as the Netflix hit series, Dark: “You can better understand those kinds of German scary movies, and their 1980s roots, if you read Gudrun Pausewang.”

    Even Pausewang’s admirers concede that the books can be painful. “It was so overwhelming, this scenario, so huge, that I didn’t know how to cope with it, as a child,” says Rémi, recalling the effect of reading The Last Children of Schewenborn. Then again, she argues, it’s a realistic depiction of how children experience systemic meltdown. “Her texts encourage readers to engage with big questions: the environment, anti-nuclear issues, but also, especially in her later years, the Nazi era, Fascism, dictatorship and political radicalisation.” And by rejecting a heroic narrative, one in which the child might triumph through some individual act of bravery or cunning, Pausewang places the responsibility squarely on the adults, and the system they created. (She also had less subtle ways of getting that message across: In The Last Children of Schewenborn, the children scrawl “Cursed Parents!” on a wall, and one of them cries: “The bomb is your fault!”.)

    Overall, Rémi says, the question that haunted Pausewang remains hugely relevant today, at a time of climate change and conflict: “What did we inherit from the past, and what are we passing on to the next generation?”

    Given that I am a member of Generation Pausewang, re-reading The Cloud for this article did make me reflect on how her gloomy outlook shaped me. I devoured her books as a child and teenager, and admire her commitment to truth-telling. But I also wish she had, perhaps, broadened her view of human nature just a little, and allowed for the possibility that people do sometimes choose to be brave, hopeful, altruistic and forgiving – and thrive. Of course, Pausewang would have found that suggestion naïve, and worse, patronising. As she once said, at the age of seven she already disliked books with a happy ending, and felt the writers didn’t take her seriously. She promised herself: “If I’m ever going to become a writer, I will take my readers seriously, regardless of whether they are six, 16 or 60. And I did become a writer, and I do take my readers seriously.”

    Sophie Hardach is a journalist and writer living in London. Her latest novel, Confession with Blue Horses, was shortlisted for the Costa Novel Award.

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  • Protests: Rocks, smoke bombs outside drag story time event

    Protests: Rocks, smoke bombs outside drag story time event

    EUGENE, Ore. — Protesters threw rocks and smoke grenades at each other outside a drag queen story time event at an Oregon pub that was to have featured an 11-year-old performer, but the weekend event went on as planned despite the confrontation.

    The 11-year-old did not take part as scheduled but was in the audience of about 50 people as some 200 demonstrators and counterdemonstrators — some of them armed — faced off outside the Oregon pub where Sunday’s story time was held.

    Authorities said people in the crowd of about 200 protesters on both sides briefly “lobbed projectiles” at each other, prompting authorities to shut down the street. Some in the crowd had semi-automatic rifles, police said. The projectiles were rocks and some smoke bombs, the Register Guard reported.

    Police did not make any arrests and said one person was taken to the hospital by ambulance with an unspecified injury.

    The tense protest made the pub in Eugene, about 110 miles (175 kilometers) south of Portland, the latest target of anti-LGBTQ rhetoric that’s increasingly targeting drag story time events around the U.S.

    The Drag Queen Story Hour, a national project conceived as a means to educate and entertain children by appealing to their imaginations, has generated social media backlash from opponents who claim they want to protect children. Organizers said the protests were actually frightening and endangering participants and they vowed to enhance security at the events but not halt their programs.

    The pub said Monday in a Facebook post that the event went on safely despite the protests, but the business expects to be “a target for violent extremists for a good while” and said it spent $2,000 on private security Sunday.

    The pub’s staff had “an intense weekend filled with racist and homophobic hate mail, physical threats of violence, and repeated attacks by right wing media outlets framing our Drag Queen Storytime as nefarious.”

    “We love you all so much, and we will not ever back down to hate,” the pub said in its Monday post. It added, “Thank you for standing with us against this growing trend of violence against queer youth and LGBTQ venues.”

    The pub frequently holds LGBTQ-friendly events and had promoted the show as a story time featuring drag performers singing songs and reading picture books, with plans to include the 11-year-old performer.

    Inside the pub, the child who had been expected to perform instead became the show’s guest of honor as several adult drag queens sang and read picture books before an audience that included families with small children.

    An advertisement for the event had featured a rainbow, a unicorn and puffy clouds against a blue sky along with superimposed photos of the child performer and three adult drag queens.

    The 11-year-old, who goes by the stage name Vanellope, has performed at the eatery and live music venue before with little fanfare. Videos posted on the pub’s Facebook page shows her dancing and singing in a poofy white and blue dress while families with small children watch and dance along.

    Tension over the show had been brewing all week after right-wing personalities learned of it and posted about it online.

    The nonprofit Drag Queen Story Hour was started in San Francisco in 2015 by activist and author Michelle Tea. Chapters have since opened across the U.S. and elsewhere. Other organizations with readers in drag have also formed.

    As part of Drag Queen Story Hour’s programming, drag queens read to children and their parents at libraries, bookstores, fairs, parks and other public spaces to celebrate reading “through the glamorous art of drag.”

    Other drag events have also been in the headlines lately. Most recently, a half-hour “Drag Kids” program planned for the Boise Pride Festival generated national backlash and anonymous threats. Festival organizers envisioned a short performance where kids could put on sparkly dresses and lip-sync to songs like Kelly Clarkson’s “People Like Us” on stage. But organizers ultimately pulled the program from the festival due to safety concerns.

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  • Stephen Curry launches graphic novel series on sports stars

    Stephen Curry launches graphic novel series on sports stars

    NEW YORK — Stephen Curry’s latest move is one for the books.

    The NBA superstar is launching a graphic novel series, “Stephen Curry Presents!: Sports Superheroes,” in partnership with Penguin Workshop. The first of four planned installments will focus on Curry’s career and is scheduled for fall 2024.

    The series will be created through the publishing arm of Unanimous Media, the company founded by Curry and Erick Peyton. Last month, Penguin released Curry’s picture book “I Have a Superpower.”

    “We hope that when kids pick up the books in this series to read all about their favorite athletes, it not only instills excitement and grows their love for reading, but also inspires them to reach for the stars and accomplish their dreams,” Curry and Peyton said in a statement released Friday by Penguin Workshop, a Penguin Random House division.

    The new series will be written by Rich Korson and John Bycel, with illustrations by Damion Scott.

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  • Three Teachers Turned Bestselling Children’s Book Authors Team Up to Help Others Get Published Too

    Three Teachers Turned Bestselling Children’s Book Authors Team Up to Help Others Get Published Too

    Press Release


    Apr 29, 2022

    Local author and founder of At Home Author Vicky Weber always wanted to write children’s books but thought that dream was unrealistic. One day, she decided to dive headfirst into the industry to see what happened. What she found through her research was a lot of overwhelming and conflicting information…and none of it could be easily found in one place.

    “It was like trying to put a puzzle together without knowing what the picture looked like. It was defeating at times but I was determined to make my dream come true,” Weber says. Sure enough, Weber became a bestselling author within 9 months of publication and later went on to be published by Disney.

    In a conversation with fellow teacher and award-winning author Brittany Plumeri, Weber realized that it wasn’t just her who felt paralyzed with fear and overwhelmed with information at the start of the publishing process. Plumeri had felt that way too, as did countless others in the author community.

    “As licensed educators, we wanted to help. We wanted to do what we do best: teach!” Weber states. So in January of 2021, Weber, Plumeri, and Scholastic author and teacher Chelsea Tornetto created At Home Author: a coaching and consulting company specializing in children’s books to help current and aspiring authors navigate the publishing world and achieve success.

    Plumeri states: “I wanted to provide a safe place that was lacking in the author community. One that others could trust and know that at the end of the day, they’d walk away with exactly what they need – no loopholes or smokescreens. Just facts and support.”

    With Weber as the self-publishing expert, Plumeri as design & social media marketing strategist, and Tornetto as the traditional publishing specialist, the company has already helped hundreds of people write, publish, and market their children’s books – and make them stand out from the crowd.

    Connect with them on FacebookInstagramYouTube, or their website.

    If you would like more information about this topic or arrange an interview, please email contact@athomeauthor.com

    Source: At Home Author

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  • Viral Hero Turns Kitten Rescue Into an Award-Winning Children’s Book Series

    Viral Hero Turns Kitten Rescue Into an Award-Winning Children’s Book Series

    After becoming a viral sensation for rescuing a kitten that had been glued to a road in Oregon, Chuck Hawley and his rescued friend, Sticky, turn a sticky situation into an award-winning Children’s book series based on kindness, empathy, and friendship.

    Press Release


    Feb 22, 2022

    Sticky the Kitty and his super-hero dad, Chuck Hawley, have a new claim to fame: award-winning Children’s Books. “Sticky” got his name along with a new lease on life, when Chuck Hawley found him in 2018, covered in a rubber cement type of glue, and stuck to a busy road near Salem, Oregon. After stopping traffic to peel Sticky’s paws off the pavement, Chuck took him to the vet to get him cleaned up and the rest is viral history. As the story of the two new friends became an international sensation, Chuck began to receive tens of thousands of messages on social media. One message in particular, caught Chuck’s attention. The writer of this message wrote of how he had been struggling with mental health issues and having lost all hope, had been contemplating suicide. A photo that popped up on this mans computer screen, of a tiny kitten looking at a human being with such trust and admiration had given this man enough hope to decide to seek help. He thanked Chuck for saving his life. It was this message that set Chuck on a mission. A mission of giving hope and encouragement to the “underdogs” of the world. He set off writing a series of books he hoped would help children and adults through their own ‘sticky situations’. And they worked.

    Fast forward three years and the books have become an underground hit around the world, aiding teachers in their classrooms, therapists in their daily sessions, and are enjoyed by families in all 50 states and over 20 countries worldwide. The books are used everywhere from an Autistic Academy in Kentucky to a school in Kenya teaching lessons on kindness to teaching English in an orphanage in Pakistan. No matter where the books end up, the common result seems to be smiles. When asked how that makes him feel, Chuck responds saying, “What better job is there than smile maker? I’ll take it!”

    Surprised by the success of the books himself, Chuck continues, “I could have never imagined how that little kitten would change my life, but he definitely changed my life. I’m just grateful and humbled by each and every person this story and these books help. I want the underdogs to know they can win, and what bigger underdog is there than a kitten, glued to a road?”

    For more information on Sticky and Chuck’s story or Chuck’s books, visit their website at www.stickythekitty.com

    or Amazon at:

    https://www.amazon.com/Chuck-Hawley/e/B083NGH912?ref=sr_ntt_srch_lnk_3&qid=1645206819&sr=8-3

    stickythekitty503@gmail.com

    Source: Sticky the Kitty, LLC

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  • The Entrepreneurial Story Behind ‘The Elf Games’: Creator Chad Scott and Family Talk Publishing, ‘The Poster Boy’ and Building a Family Business

    The Entrepreneurial Story Behind ‘The Elf Games’: Creator Chad Scott and Family Talk Publishing, ‘The Poster Boy’ and Building a Family Business

    The entrepreneurial spirit is a common thread that’s pulled Chad Scott and his family closer with the release of their new book ‘The Elf Games’

    Press Release



    updated: Nov 5, 2020

    ​Author and entrepreneur Chad Scott continues to build on the strong business foundation he’s created with the release of this year’s hottest holiday children’s book: The Elf Games

    But, to get to this point in his book-publishing career, Chad started with the release of The Poster Boy: Small Towns, Big Ideas, and the Reality of Becoming an Entrepreneur. 

    “I wrote, ‘The Poster Boy’ to give entrepreneurs a head start in business and learn how to create an organization that gives as good as it gets,” said Scott, “Entrepreneurship isn’t for the faint of heart and in this book, readers have the opportunity to learn from my stupid mistakes, ridiculous problems, and innovative solutions to come away with real-world hiring and funding advice and the motivation to start their business, today.”

    This solo venture ultimately moved him to build something with his family and, from there, they embarked on their book-writing adventure. 

    “My experience writing The Poster Boy helped me recognize the opportunity to talk about the lessons and value of hard work and determination that were instilled in me as a kid,” noted Scott. “This time around, I wanted to work on a book with my wife and kids that highlighted the importance of sports in children’s lives and bring those lessons to life with a holiday theme.”

    The Elf Games is a story that emphasizes teamwork and Chad, along with his wife and kids, exemplified this lesson as they worked together to write this book for families all over the country. 

    From The Poster Boy to The Elf Games, Chad’s ultimate goal is to build a family business with the ones he loves while covering the topics that share fundamental lessons and values that are necessary to build a strong and empathetic society moving forward. 

    Enjoy some quality family bonding over the heartwarming tale of The Elf Games this holiday season.

    About ‘The Elf Games’

    From sportsmanship to empathy and everything in between, “The Elf Games” shares valuable and inspiring lessons within this beautifully written and illustrated holiday title. In fact, Peter Foyo has said “The Elf Games” is “The most beautifully illustrated and unique Christmas story for kids in 2020!” The holidays are around the corner and “The Elf Games,” which combines education with entertainment, is the perfect story that young readers are sure to enjoy. 

    CONTACT INFORMATION:
    Tiffany Kayar
    tiffanyPR@newswirecontact.com

    Source: Chad and Mary Scott

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  • Children’s Adventure Book ‘The Noodle Society’ for True Pasta Lovers

    Children’s Adventure Book ‘The Noodle Society’ for True Pasta Lovers

    The story follows four young chefs from the U.S., France, Japan and Switzerland on their trip to the secret Noodle Society Headquarters.

    Press Release



    updated: Aug 18, 2017

    Swiss Author Stephan Lendi has released his new book “The Noodle Society”, which is a children’s adventure tale that follows four talented young chefs on their trip to the secret Noodle Society Headquarters. The story includes fun facts on the history of noodles and the way noodles are prepared and eaten around the world. It inspires young readers to follow their passion for cooking and discover new flavors and textures while expanding their cultural horizons.

    In the story, Jill from the U.S., Liliane from France, Miko from Japan, and Peter from Switzerland take part in competing against one another with their own noodle dishes to become a member of the Noodle Society – a secret society of only the most talented noodle chefs. As the children move through the various rounds of the competition, they advance their recipes and refine their cooking techniques and passion for noodles. They also develop an understanding of the cultural background of their competitors. Through the story, readers come to know the characters and wonder which young chef will convince the jury they are the best and be given the honor of becoming a member of the secret Noodle Society.

    Lendi, who currently resides in Zurich, is a Swiss marketing and communications professional with a passion for food and cooking. When he was taught to fold Gyozas the Japanese way by his Japanese friend’s grandmother, he fell in love with the Japanese cuisine from Izakaya style cooking to high-end Kaiseki creations.

    “The story was really grown out of my passion for cooking and travel,” says Lendi. “I have always loved to travel, especially to Japan, China, various European countries, the U.S., and Canada. I find a lot of joy in discovering the stories of the people I meet on my journeys, tasting local food, and talking to local chefs about their stories and passions.”

    Lendi is also the CEO of Newbury Media & Communications. During his professional career as a communications coach, he has specialized in body language, professional speaking, voice and moderation skills coaching. With more than 15 years as one of the leading voiceover artists in Switzerland and corporate voice of many globally known companies, Lendi feels at home behind the microphone and onstage as the host of various corporate events, panel discussions and cooking shows.

    “The Noodle Society” is available as an e-book for Kindle on Amazon, softcover on Amazon, and as an audiobook on Audible.

    About Newbury Media & Communications Ltd

    Newbury Media & Communications is the communications agency of Swiss communications professional Stephan Lendi. He is a keynote speaker and author of various books. For more information, visit Newbury.ch.

    Press Contact 

    Stephan Lendi
    +41 79 501 56 59
    lendi@newbury.ch

    Source: Newbury Media & Communications Ltd

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  • Mutasia Launches “Figley’s Search for the Perfect Pet”

    Mutasia Launches “Figley’s Search for the Perfect Pet”

    Mutasia to Launch Latest Book with a Series of Children’s Special Author and Illustrator Events

    Press Release



    updated: Mar 9, 2017

    ​Mutasian Entertainment, LLC (www.mutasia.com), a children’s creative entertainment company, is launching its latest hardcover children’s book, ‘Figley’s Search for the Perfect Pet’, for children ages 4-8, on April 5, 2017, with a series of author and illustrator days at Barnes & Noble bookstores.

    Author, Suzanne Cotsakos, and author-illustrator, Ryan McCulloch, of ‘Figley’s Search for the Perfect Pet’ will be hosting special interactive events, consisting of book signings, readings, and character drawing tips at various Barnes & Noble bookstores. The events will be open to the public during national story time on Saturday mornings, beginning on April 8, 2017 at the Arden Fair Barnes & Noble in Sacramento.  

    ‘Figley’s Search for the Perfect Pet’ is set on the island of Mutasia, where everyone is a mix of two or more different animals, making it hard to find the perfect pet. But if anyone is up for the challenge, it’s Figley. When his friend, Billie, admits that she’s grown tired of her boring pet pugapillar (a pug-caterpillar mix), Figley sets out to find her the weirdest, wildest, and wackiest pets on the island. He introduces Billie to an assortment of mixed-up critters like a dolphin-pony, lizard-cat, and flamingo-elephant-goldfish; and each critter presents an unexpectedly troublesome trait. As the exotic critters begin destroying her house, Billie starts to reassess what’s really important in a perfect pet.

    In addition to the events at Barnes & Noble bookstores, Mutasia, an eight-time winner of the prestigious Mom’s Choice Award and numerous international Honorable Mentions, will also be presenting ‘Figley’s Search for the Perfect Pet’ to elementary schools around the country.

    ‘Figley’s Search for the Perfect Pet’ is being distributed through Midpoint Trade Books and will be available wherever books are sold, including Amazon, Books A Million, Target and Barnes & Noble.

    In addition to books, Mutasia has developed an animated TV-pilot, original music, plush toys, as well as mobile coloring book apps available on the iPhone and iPad.

    Like the inhabitants of Mutasia, the Mutasian Entertainment family is comprised of unique individuals who have come together and blended their talents in an effort to create a world that will encourage children to explore the outer limits of their imaginations through stories, music, and art.  Mutasia strives to “Mix It Up” by creating an environment that encourages creativity and teaches about life’s many lessons in a fun and humorous way.

    For further information, visit Mutasia at:

     www.mutasia.com or www.facebook.com/mutasia

    ‘Figley’s Search for the Perfect Pet’

    Initial Barnes & Noble Tour Dates – Open to the Public

    April 8th – Sacramento, CA (1725 Arden Way)

    April 22nd – Santa Monica, CA (3rd Street Promenade)

    April 23rd – Studio City, CA (12136 Ventura Boulevard)

    April 29th – West Hollywood, CA (189 The Grove)

    Media Contact:
    Liz Rodriguez, EMR Media
    310 435 3634
    liz@emrmedia.com

    Source: Mutasian Entertainment LLC

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  • Gifted Boy Inspires Subscription Box Boosting Accessibility of African-American Children’s Literature

    Gifted Boy Inspires Subscription Box Boosting Accessibility of African-American Children’s Literature

    Finding children’s literature featuring characters of color is now a lot easier for parents with the subscription box service, Little Buzz Book Club.

    ​​​​​Inspired by a young boy who taught himself how to read at the age of two, the Little Buzz Book Club is a monthly delivery of exciting new and classic children’s books featuring African, Caribbean and African-American Cultures. But it’s not just African-American children’s literature that’s featured in the monthly subscription box. There are also games, a card from Little Buzz and educational tool kits for parents.  What’s more is that there is also an authentic African keepsake in every box.

    Most African-American parents understand how challenging it can be to find books for black children and statistics from Cooperative Children’s Book Center (CCBC) attests to this. CCBC receives most of the trade books published annually in the United States. In 1985, only 18 of the 2,500 trade books that were published were written by African Americans. Although this number has improved over the decades, statistics still indicate that there is still a diversity gap when it comes to children’s book. CCBC’s 2015 statistics revealed that of all the children’s books received by the Center, only 7.59% featured people of color.

    “I was disappointed that I had such a difficult time finding books for my son who loved reading but didn’t see himself in many books. Then I realized there were millions of other moms who wanted to inspire their children with stories about characters that looked like them as well.”

    Dr. Hamidah Sharif-Harris, Founder of Little Buzz Book Club

    Little Buzz Book Club is on a mission to promote books about people of color including African and Caribbean culture. The Little Buzz character was inspired by the Founder’s six-year-old son, Qadar. At the age of two, Qadar taught himself how to read. He has a rare condition known as hyperlexia – a natural ability to decode and understand words without the ability to speak in conversation. Qadar had a hard time communicating with others but eventually began to mimic conversations he read in the books. As a result, he has developed a love for reading and enjoys putting himself inside of books.

    When asked about the motivation to start the subscription box, Sharif-Harris said: “I was disappointed that I had such a difficult time finding books for my son. Then I realized there were millions of other moms who wanted to inspire their children with stories about characters that looked like them as well.”
    Little Buzz Book Club is the first subscription box that focuses on literature featuring children of color. For this reason it has been generating a buzz among the African-American and Caribbean communities.  The club has more than 33,000 Facebook fans and the number of satisfied subscribers continues to grow. One parent commented: “Asiri was so happy to get her subscription box. It was the first time she did work on her own. Great investment!”

    The subscription box is affordable and features two plans – one for preschoolers and the other for young readers’ ages 4-10 years old. The pre-school subscription box is available for $14.95 and the young reader subscription box for $18.95. For further details or to start a subscription, visit: https://www.littlebuzzbookclub.com

    Source: Little Buzz Book Club

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