by Robert Skead & Mike Simmel ‧ RELEASE DATE: Sept. 15, 2011
Fourteen-year-old Mike is about to take what might become the winning shot for his travel basketball team when he reflects...
A teen with epilepsy has fantastic basketball skills, honed by years of relentless practice, but still struggles frequently with his condition.
Fourteen-year-old Mike is about to take what might become the winning shot for his travel basketball team when he reflects back on his 12 years of living with epilepsy. His path to success has veered around roadblocks: seizures that aren’t fully controlled by his medicines, bullying at school and prejudice on the part of his coach and a few other adults. With knowledgeable parents, a good doctor and a wise counselor, he’s doing well; this aspect rings true, since one of the authors, Simmel, has had epilepsy since early childhood and is also a member of the Harlem Wizards, a performing basketball team. Stock characters and heavy-handed asides reinforce the helpful message to readers but often intrude on the storytelling unnecessarily: “His mom also reminded him that it’s normal to be embarrassed or upset if kids didn’t understand his epilepsy.” This weakness diminishes the novel’s potential to reach a broad audience. A lengthy afterward provides a wealth of accurate and useful information for patients and their families.Pub Date: Sept. 15, 2011
ISBN: 978-1-4338-1043-5
Page Count: 80
Publisher: Magination/American Psychological Association
Review Posted Online: July 19, 2011
Kirkus Reviews Issue: Aug. 1, 2011
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by Robert Skead ; illustrated by Floyd Cooper
by Jacqueline Woodson ‧ RELEASE DATE: Sept. 1, 2020
A poignant and achingly beautiful narrative shedding light on the price of a violent sport.
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Coretta Scott King Book Award Winner
An African American preteen finds his world upended when his father, a retired professional football player, displays symptoms of traumatic brain injury.
Twelve-year-old Zachariah “ZJ” Johnson Jr. loves his dad but wonders who he would be if his dad was not a famous athlete. Although his dad is in the spotlight, he is full of love and attention for ZJ and his friends. And fortunately, ZJ has three friends who see him and not his father’s shadow. “Zachariah 44” was a fearless player who suffered many concussions during his playing career. The changes in his father begin slowly and intermittently. Soon the headaches and memory lapses grow increasingly frequent and scary for ZJ and his mom, since the doctors do not seem to have any answers. As his dad slips further away, ZJ’s memories of better times grow closer than ever. Using spare and lyrical language for ZJ’s present-tense narration, which moves back and forth through time, Woodson skillfully portrays the confusion, fear, and sadness when a family member suffers from brain injury and the personality changes it brings. Readers see Zachariah Sr. through ZJ’s eyes and agonize with him as the strong, vibrant athlete begins to fade. The well-rounded secondary characters complete a mosaic of a loving African American family and their community of friends. The tale is set in the early 2000s, as awareness of chronic traumatic encephalopathy and its catastrophic consequences was beginning to emerge.
A poignant and achingly beautiful narrative shedding light on the price of a violent sport. (author's note) (Historical fiction. 10-14)Pub Date: Sept. 1, 2020
ISBN: 978-0-399-54543-6
Page Count: 176
Publisher: Nancy Paulsen Books
Review Posted Online: June 29, 2020
Kirkus Reviews Issue: July 15, 2020
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by Jacqueline Woodson ; illustrated by Leo Espinosa
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by Jacqueline Woodson ; illustrated by Rafael López
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by Chad Morris & Shelly Brown ‧ RELEASE DATE: Oct. 3, 2017
Medically, both squicky and hopeful; emotionally, unbelievably squeaky-clean.
A 12-year-old copes with a brain tumor.
Maddie likes potatoes and fake mustaches. Kids at school are nice (except one whom readers will see instantly is a bully); soon they’ll get to perform Shakespeare scenes in a unit they’ve all been looking forward to. But recent dysfunctions in Maddie’s arm and leg mean, stunningly, that she has a brain tumor. She has two surgeries, the first successful, the second taking place after the book’s end, leaving readers hanging. The tumor’s not malignant, but it—or the surgeries—could cause sight loss, personality change, or death. The descriptions of surgery aren’t for the faint of heart. The authors—parents of a real-life Maddie who really had a brain tumor—imbue fictional Maddie’s first-person narration with quirky turns of phrase (“For the love of potatoes!”) and whimsy (she imagines her medical battles as epic fantasy fights and pretends MRI stands for Mustard Rat from Indiana or Mustaches Rock Importantly), but they also portray her as a model sick kid. She’s frightened but never acts out, snaps, or resists. Her most frequent commentary about the tumor, having her skull opened, and the possibility of death is “Boo” or “Super boo.” She even shoulders the bully’s redemption. Maddie and most characters are white; one cringe-inducing hallucinatory surgery dream involves “chanting island natives” and a “witch doctor lady.”
Medically, both squicky and hopeful; emotionally, unbelievably squeaky-clean. (authors’ note, discussion questions) (Fiction. 9-11)Pub Date: Oct. 3, 2017
ISBN: 978-1-62972-330-3
Page Count: 256
Publisher: Shadow Mountain
Review Posted Online: Aug. 1, 2017
Kirkus Reviews Issue: Aug. 15, 2017
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by Chad Morris & Shelly Brown ; illustrated by Garth Bruner
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by Chad Morris & Shelly Brown
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by Chad Morris & Shelly Brown ; illustrated by Garth Bruner
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