Medical Biography

In No Woman Left Behind, Grant recounts her decision to abandon a promising advertising career, and the ups and downs of building Silicon Valley–based Fistula Foundation from a modest start-up into the global leader in fistula treatment. Through vivid firsthand accounts of surgeons toiling in remote corners of Africa and Asia, we see inside the fight to restore hope to some of the world’s most vulnerable women.

In this debut collection of essays, Pace tells of his years as a career paramedic—wandering through the highs and the lows, the saves and the losses, the patients he remembers, and the ones he tries to forget. In 1997, Pace began his career as an EMT because he wanted to do something exciting. He wanted to help people too. And he thought those two things—excitement and helping people—would exist hand in hand. With a little sprinkle of glory thrown in for good measure.

In his early 20s, Mindy Greiling's son, Jim, was diagnosed with schizoaffective disorder after experiencing delusions that demanded he kill his mother. At the time, and for more than a decade after, Greiling was a Minnesota state legislator who struggled, along with her husband, to navigate and improve the state's inadequate mental health system. Fix What You Can is an illuminating and frank account of caring for a person with a mental illness, told by a parent and advocate.

From his early years with his loving Jewish family to the horrors of Auschwitz to his life as a Nobel Prize-winning writer, Elie Wiesel tells his story. Passionate and poignant, All Rivers Run to the Sea is an unforgettable book of love and rage, doubt and faith, despair and trust, and ultimately, of wisdom.

Welcome to Bryson City, a small town tucked away in a fold of North Carolina's Smoky Mountains. The scenery is breathtaking, the home cooking can't be beat, the Maroon Devils football team is the pride of the town, and you won't find better steelhead fishing anywhere. But the best part is the people you're about to meet in Bryson City Seasons. In this joyous sequel to his bestselling Bryson City Tales, Dr. Walt Larimore whisks you along on a journey through the seasons of a Bryson City year.

The book is written with humour on a subject which could very easily be melancholy, and whilst not avoiding the truth about this degenerative neurological condition, Simon takes you on a journey with earnest compassion. A great listen for everyone, especially for anyone remotely connected to Parkinson’s Disease, this is an uplifting, supportive and reaffirming listen; life is still to be enjoyed no matter what the adversity.

Living By My Rules, an eloquent insight into the daily struggles of living with an incurable, degenerative disease such as Parkinson’s disease. Simon’s stories of his early life will transport you back to a far simpler time; the 1970s. Amusing tales which will stir fond memories in all but the youngest listeners… Flares, scooters, Mods and of course a nostalgic look back at his beloved football; especially QPR.

Ingram's first-hand account of his life from his early childhood to teen years to his first signs of the debilitating disease give an insider's look at not just a 'disease' but a man.

This is the autobiography of one woman’s life, beginning with her difficult childhood, the later devastating diagnosis of multiple sclerosis and the early effect it had on her, through to her discovery of a lifestyle that has had positive repercussions on her condition. She meets all obstacles with determination not to let them defeat her and regards these with a cheerful attitude seeing a positive side to them.

Tim Booth is shocked when his first emergency call-out for someone short of breath turns out to be an adult man with a blocked nose. Far from beginner's luck, this turns out to be an omen for the rest of his paramedic career. Between the obligatory stories of objects lodged in body cavities to grown men who can't look after themselves when their wives are away, Tim finds that the promised life-saving moments are far outweighed by the trivial, frustrating and bizarre ambulance callouts.

This book is a physician’s reflection on his 40-plus years of interactions with family, friends, patients, medical students, and residents. The short stories are meant to show how humanism, professionalism, and ethical behavior can enrich one’s life and those of others. The path leading to the insights is laid out for the listener using humor and reflection. All the stories are true and arranged to show how we all grow in our approach to life. Every moment in our life is worth experiencing and each opens an often unexpected door for us.

The word “refugee” sparks conversation and fuels emotion. There are more than 22 million refugees worldwide and another 65 million who have been forcibly displaced. But who are these people? Images filter into our consciousness via dramatic photographs - but these photos only offer a glimpse into their stories. As a young ER nurse in Boston, Roberta Gately was stopped cold by stark images of big-bellied babies with empty haunting stares in the news. She called the aid organization featured in the news story, and, within two months, she had become a humanitarian aid worker.

"Le voyage - ce voyage-là du moins - est pour moi terminé. A partir de demain, mieux : à partir de cet instant, tout est neuf. Je poursuis mon chemin. Demain, comme tous les jours d'ici ou d'ailleurs, sur ce versant ou sur l'autre, est désormais mon jour de naissance."

Dr. Joel Salinas is a Harvard-trained researcher and neurologist with extraordinary gifts that provide him unique access to his patients and enable him to experience life in an extraordinary way. He has mirror-touch synesthesia, a neurological trait that allows him to feel others' emotions and physical sensations. Susceptible to the pain and discomfort of his patients, Salinas uses his heightened empathic ability - what he calls "compulsory mindfulness" - to help understand and better treat their conditions.

In 1959, a Cincinnati pharmaceutical firm, the William S. Merrell Company, quietly began distributing samples of an exciting new wonder drug already popular around the world. Touted as a sedative without risks, thalidomide was handed out freely, under the guise of clinical trials, by doctors who believed approval by the Food and Drug Administration was imminent. But in 1960, when the application for thalidomide landed on the desk of FDA medical reviewer Frances Kelsey, she quickly grew suspicious.

Pro football Hall of Famer Jim Kelly and his wife, Jill, were catapulted from a seemingly fairy-tale life of celebrity into a world of private struggle and medical uncertainty. What the public didn’t know, however, was that behind the scenes lurked more than a family’s pain at the dire prognosis of their only son. Hunter’s illness exposed the troubled depths of a marriage that had long been shadowed by uncertainties of its own.

In the opening of Holding Silvan: A Brief Life, Monica Wesolowska gives birth to her first child, a healthy-seeming boy who is taken from her arms for "observation" when he won't stop crying. Within days, Monica and her husband have been given the grimmest of prognoses for Silvan, and they must make a choice about his life. The story that follows is not a story of typical maternal heroism. There is no medical miracle here. Instead, we find the strangest of hopes.

LiveReal recounts a family's journey through their daughter's liver transplant. It is a story of faith and miracles, following a life-threatening diagnosis of Biliary Atresia. This story provides a candid portrait of the fears, struggles, and hard decisions that her loving parents had to face. From a Kasai surgery to the prospect of a second transplant, the family experienced the beauty and heartache of life events.

In ADHD and Me, he tells about the next 12 years as he learns to live with both the good and bad sides of life with ADHD. Blake's memoir offers, for the first time, a young person's account of what it's like to live and grow up with this common condition. Join Blake as he foils bullies, confronts unfair teachers, struggles with distraction and disorganization on exams, and goes sailing out-of-bounds and ends up with a boatload of spiders.

A decade after World War II, there was still no such thing as open-heart surgery, and yet half a million Americans were dying from heart disease every year. After the first daring operation in 1954 and through the next three decades, five heroic surgeons braved the scorn of their peers, withstood fierce desperation, and faced possible death in order to devise procedures that would save overwhelming numbers of those doomed children and provide hope for a new life to all manner of heart-failing individuals.