health

"Mallory Smith shares her innermost thoughts while living with a terminal illness"--Provided by publisher.

"One summer day, nine-year-old Keira Ball was in a terrible car accident and suffered catastrophic brain injuries. As the rest of her body began to shut down, her heart continued to beat. In an act of extraordinary generosity, Keira's parents and siblings immediately agreed that she would have wanted to be an organ donor. Meanwhile nine-year-old Max Johnson had been in a hospital for nearly a year, valiantly fighting the virus that was causing his young heart to fail. When Max's parents received the call they had been hoping for, they knew it came at a terrible cost to another family-in what Clarke calls "the brutal arithmetic of transplant surgery." The act of Keira's heart resuming its rhythm inside Max's body was a medical miracle. But this was only part of the story. While waiting on the transplant list, Max had become the hopeful face of a campaign to change the UK's laws around organ donation. Following his successful surgery, Keira's mother saw the little boy beaming on the front page of the newspaper and knew it was the same boy whose parents had recently sent her an anonymous letter overflowing with gratitude for her daughter's heart. The two mothers began to exchange messages and eventually decided to meet"--Provided by publisher.

"A memoir from the point of view of a girl growing up with a severe form of cerebral palsy and preparing for an experimental surgery to address her condition"--Provided by publisher.

"When Steph Catudal met her husband Rivs, she thought that the love, stability, and warmth she shared with her husband had finally dispelled her pent-up anger and grief over the loss of her father and her faith. But when Rivs became ill and was put into coma at the height of the pandemic, the painful memories of her childhood--watching her father die of cancer--came flooding back. Written with lush lyricism, Steph's account of how this crisis forced her to confront her past is raw, illuminating, and heartbreaking: her father's death that wrecked her faith in God and jumpstarted a decade of rebellion, including running away from home and living out of a van at age sixteen, struggling with alcoholism, and delving into drugs to ease her pain. Sitting by Rivs's bedside, she grappled with the memories of the past and the uncertainties of the future while reckoning with the unknowns of her husband's illness. Rivs would endure a grueling eighty-four days in a medically induced coma, eventually undergoing chemo for a similar illness that stole her father. 'Everything All At Once' is a heart-wrenching and ultimately uplifting reflection on resilience and a powerful reminder that we can find healing no matter how broken we are"--.

"In 2011, three years after leaving the NFL, Steve Gleason was diagnosed with ALS, a terminal disease that takes away the ability to move, talk, and breathe. Doctors gave him three years to live. He was thirty-three years old. As Steve says, he is now ten years past his expiration date. His memoir is the chronicle of a remarkable life, one filled with optimism and joy, despite the trauma and pain and despair he has experienced. Writing using eye-tracking technology, Gleason covers his pre-ALS life through the highs and lows of his NFL career with the New Orleans Saints, where he made one of the most memorable plays in Saints history, leading to a victory in the first post-Katrina home game, uplifting the city, making him a hero, and reflected in a nine-foot bronze statue outside the Superdome. Then came his heartbreaking diagnosis. Gleason lost all muscle function, he now uses Stephen Hawking-like technology to communicate, and breathes with the help of a ventilator. This book captures Gleason and his wife Michel's unmatched resilience as they reinvent their lives, refuse to succumb to despair, and face his disease realistically and existentially. This unsparing portrait argues that a person's true strength does not reside solely in one's body but also in the ability to face unfathomable adversity and still be able to love and treasure life"--.

"Mallory Smith shares her innermost thoughts while living with a terminal illness"--Provided by publisher.

Lu Spinney's memoir Beyond the High Blue Air is at once a portrait of the fearlessness of familial love and the profound dilemma posed by modern medicine. When Spinney's twenty-nine-year-old son, Miles, flies up on his snowboard, "he knows he is not in control as he is taken by force up the ramp," writes his mother, "skewing sideways as his board clips the edge and then he is hurtling, spinning up, up into the free blue sky ahead . . ." He lands hard on the ice and falls into a coma. Thus begins the erratic loss--Miles first in a coma and then trapped in a fluctuating state of minimal consciousness--that unravels over the next five years. Spinney, her husband, and three other children put their lives on hold to tend to Miles at various hospitals and finally in a care home. They hold out hope that he will be returned to them. With blunt precision, Spinney chronicles her family's intimate experience.

"Twenty-something author, blogger, and entrepreneur Shane Burcaw . . . [presents] an essay collection about living a full life in a body that many people perceive as a tragedy. From anecdotes about first introductions where people patted him on the head instead of shaking his hand, to stories of passersby mistaking his able-bodied girlfriend for a nurse, Shane tackles awkward situations and assumptions with humor and grace"--Provided by publisher.

"A fresh, fierce, and timely meditation on data, pain, time, and the limited capacity of literature to comprehend life and death in a sensate and vulnerable body"--Provided by publisher.

"How do you keep going when you have received the worst possible diagnosis? This is what happened to Jessica Morris when, in her early fifties, she was told she had glioblastoma (GBM), a particularly aggressive and difficult-to-treat form of brain cancer. All In My Head is her brilliant, brave and inspiring riposte. Jessica began a determined search for effective treatment as she continued to live her life, love her family and campaign for better research into GBM, connecting with patients all over the world. And finally, she came to terms with the knowledge that she had reached the end of the road. Much more than a book about GBM, it takes readers into the life of a woman who when confronted by devastating news chooses to be strong"--Provided by publisher.