Showing results for "Family" in Medical

Unlocked begins with a vivid depiction of the author's life with her autistic son, Ben. Feelings of isolation and self-hate and even moments of hatred toward her own child in response to his behaviors, as well as the impact on her marriage and younger daughter, impel her to seek solutions for his condition. Through years of trial and error, Susan eventually discovers methods that bring about radical improvement in Ben.

“Strokes are the third-leading cause of death in America, and for the ‘lucky’ stroke victims who don’t die, about half will spend the rest of their lives trying to recover.” Roughly 700,000 American suffer a stroke each year and around 140,000 of them are fatal. Different Strokes is an in-depth look at what surviving, or not surviving, a stroke can mean.

On a sunny spring day, in an ordinary kitchen, Rosemary answers an unexpected phone call. A car has hit her husband, Hugh. Rosemary arrives at the hospital just in time to see him before he's rushed into surgery. Thinking of their twin daughters, Rosemary pleads with her unconscious husband as he lies on a gurney. "Don't you leave me Hugh Rawlins. Anna and Mary need you. I love you." Overwhelmed, but determined to bring Hugh back home, Rosemary leans on family and friends as Hugh endures two emergency brain surgeries, a coma, and a confused awakening.

Cystic fibrosis was once a mysterious disease that killed infants and children. Now it could be the key to healing millions with genetic diseases of every type - from Alzheimer's and Parkinson's to diabetes and sickle cell anemia. Told from the perspectives of the patients, families, physicians, scientists, and philanthropists fighting on the front lines, Breath from Salt is a remarkable story of unlikely scientific and medical firsts, of setbacks and successes, and of people who refused to give up hope....

NEW YORK TIMES EDITORS’ CHOICE In this vulnerable, insightful memoir, the New York Times columnist tells the story of his five-year struggle with a disease that officially doesn’t exist, exploring the limits of modern medicine, the stories that we unexpectedly fall into, and the secrets...

In this heart-wrenching memoir by a renowned transplant doctor who grew up without religion, a journey of self-discovery as he uncovers his family's past. David Weill grew up in New Orleans the only son of a world-famous Jewish pulmonologist and a Southern Baptist mother. Religion was never...

When Joselin Linder was in her twenties, her legs started to swell. She thought little of it, until her health problems started to compound in ways that baffled her doctors. Diagnosed with extreme liver blockage and dangerous levels of lymph fluid, Joselin turned to the most similar case she...

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Calling all animal lovers! A heartwarming memoir about one woman's career as a vet and the unique role pets play in our lives “Filled with compassion and wisdom, Karen Fine is a healer whose own wounds have deepened her gifts for bringing animals and their people comfort and peace...

'Heartbreaking and inspiring in equal measure. A must-read.' Andy Burnham, Mayor of Greater Manchester 'Nicola is a beautiful human being and her story is full of the joys and sorrows of humanity.' Cathy Rentzenbrink The inspiring, life-affirming memoir from Nicola Nuttall about her incredible...

A Short History of Falling – like The Diving Bell and the Butterfly, and When Breath Becomes Air – is a searingly beautiful, profound and unforgettable memoir that finds light and even humour in the darkest of places. We keep an old shoebox, Gill and I, nestled in a drawer in our room...

Experts agree on the value of genetic testing when there is a family history of disease, or if the patient has an illness frequently caused by a mutation. Knowing the disease mutation lets family members find out if they have it too and need preventive care. The book explains that doctors can order tests with genetic counseling at relatively low cost and how this will help them prescribe preventive actions, make earlier diagnoses, and get better outcomes.

Mitreißend erzählt: Eine Familiengeschichte, generationenübergreifend geprägt von Alkoholabhängigkeit. Mia ist die jüngste Tochter in einer langen Dynastie von Trinkenden. Auch sie selbst liebt Rotwein, aber so schlimm wie bei ihrer verrückten Oma und ihrem rätselhaften Vater, die sich mit dem Trinken umgebracht haben, ist es bei ihr noch lange nicht, denkt sie. Sie ist eben ein Partygirl, eine Rebellin, eine Künstlerseele. Bei der Arbeit als Barkeeperin im Berliner Nachtleben lernt sie, zu trinken, von einem älteren Mann lernt sie Sex und Drama.

Diagnose: Autoimmune Hepatitis. Und das mit Anfang 30. Für Hendrik und Denise Verst bricht 2015 die Welt zusammen. 5 Jahre später braucht Hendrik dringend eine neue Leber. Die 7-köpfige Familie steht vor großer Ungewissheit: Wird Papa rechtzeitig ein passendes Spenderorgan bekommen? Jetzt, 2 Jahre nach der Transplantation, arbeiten Denise aka Mathellaslife und Hendrik aka fitdad_hendrik die Zeit des Bangens und Hoffens in einem gemeinsamen Buch auf - bewegend, ehrlich und aufschlussreich.

On February 21, 1992, 22-year-old Brian Bechtold walked into a police station in Port St. Joe, Florida, and confessed that he’d shot and killed his parents in their family home in Silver Spring, Maryland. He said he’d been possessed by the devil. He was eventually diagnosed with schizophrenia and ruled “not criminally responsible” for the murders on grounds of insanity. But after the trial, where do the "criminally insane" go?

The personally harrowing and medically enthralling story of a family's struggle to save a child from a deadly immune deficiency. A journey through the deepest valleys and highest peaks of parenting. When a two-month-old baby falls ill, his apparently ordinary symptoms turn out to signal a rare...

As a happily married, 55-year-old professional woman, Susan had it all-or thought she did - until the day of her shocking diagnosis with stage IV Mantle Cell Lymphoma, a rare and aggressive disease. Ninety-eight percent of her bone marrow was cancerous, and a heart attack or brain aneurism was imminent. Within minutes of being admitted to the hospital, her beautifully ordinary life disappeared.

In Mercies in Disguise, acclaimed New York Times reporter and best-selling author Gina Kolata tells the story of the Baxleys, an upstanding family in small-town South Carolina. Many of them were doctors, but still, they are struck down by an inscrutable illness. Finally they discover the cause of the disease after a remarkable sequence of providential events. Meanwhile science, progressing for 50 years along a parallel track, handed the Baxleys a question - not a cure but a blood test that would reveal who had the gene for the disease.

Lorena Junco Margain - passionate art collector and devoted wife and mother - is already shaken after abruptly fleeing Mexico and relocating in the USA with her family while pregnant due concerns for their safety. Then, she learns she has a tumor on her adrenal gland. Rather than improve after surgery, her condition worsens. On the Way to Casa Lotus is the gripping true story of Junco Margain’s journey coming to terms with the permanent consequences of a surgeon’s devastating mistake.

Growing up in a New Jersey factory town in the 1980s, Daisy Hernández believed that her aunt had become deathly ill from eating an apple. No one in her family, in either the United States or Colombia, spoke of infectious diseases, and even into her 30s, she only knew that her aunt had died of a rare illness called Chagas. But as Hernández dug deeper, she discovered that Chagas - or the kissing bug disease - is more prevalent in the United States than the Zika virus.