Medical Memoirs

The Lobotomist explores one of the darkest chapters of American medicine: the desperate attempt to treat the hundreds of thousands of psychiatric patients in need of help during the middle decades of the 20th century. Into this crisis stepped Walter Freeman, MD, who saw a solution in lobotomy, a brain operation intended to reduce the severity of psychotic symptoms. Drawing on Freeman's documents and interviews with Freeman's family, Jack El-Hai takes a penetrating look at the life and work of this complex scientific genius.

A hopeful look at coping with the ravages of serious chronic illness by an accomplished journalist, a contributing columnist for the New York Times, and former senior producer of the CBS Evening News.

Born in rural Mexico, Eduardo “Lalo” García Guzmán and his family left for the United States when he was a child, picking fruits and vegetables on the migrant route from Florida to Michigan. He worked in Atlanta restaurants as a teenager before being convicted of a robbery, incarcerated, and eventually deported. Lalo landed in Mexico City as a new generation of chefs was questioning the hierarchies that had historically privileged European cuisine in elite spaces. At his acclaimed restaurant, Máximo Bistrot, he began to craft food that narrated his memories and hopes.

Ed Patrick is an anaesthetist. Strong drugs for his patients, strong coffee for him. But it's not just sleep-giving for this anaesthetist, as he navigates emergencies, patients not breathing for themselves and living with a terrifying sense of responsibility. It's enough to leave anyone feeling numb. But don't worry, there's plenty of laughing gas to be had.

By following the struggle for survival of one small-town hospital, and the patients who walk, or are carried, through its doors, The Hospital takes listeners into the world of the American medical industry in a way no audiobook has done before. Americans are dying sooner, and living in poorer health. Alexander argues that no plan will solve America’s health crisis until the deeper causes of that crisis are addressed.

Deeply touching and uplifting, What You See When You Can't See offers a way of looking at the world through different eyes and a road map to finding bliss in the simplest of things. Zena was born with Marfan Syndrome, a connective tissue disorder leaving her nearly completely blind, yet she kept this condition hidden from the world for four decades - until she met Munch. A guide dog with a huge personality, Munch made Zena's invisible disability suddenly plain for all the world to see. This book shares the story of Zena's journey with Munch....

Julia Pylypenko is a young writer and scriptwriter in the field of PR. She speaks English, French, and Italian. In 2007, she became the world champion in singles and doubles tennis at the XVI World Championship for people with transplanted organs (Bangkok). Ten years ago, Ukrainian doctors sentenced Julia to pass away by her eighteenth birthday. This book is a diary and a confession, where each line is not the author's imagination, but real events from her life.

In this unflinching and riveting coming-of-age memoir, Patricia Grayhall battles sexism in a male-dominated profession. She plunges into a life that is never boring—and certainly never without passion. Tossed around in the rough seas of medical training, chronically exhausted and emotionally drained, Patricia chafes at the toxic masculinity of the culture of medicine facing many of the same issues women face in male-dominated fields today.

In this highly personal account, Dr Gibbs documents the effect his diagnosis has had on his life and explains his advocacy for improving early recognition of Alzheimer’s. Weaving clinical knowledge from decades caring for dementia patients with his personal experience of the disease, this is an optimistic tale of one man’s journey with early-stage Alzheimer’s disease.

As young adults, John and Kara—father and daughter—had much in common. Avid sports lovers. Life of the party. Abiding faith in God. And a diagnosis that blindsided and benched them: aggressive, terminal cancer. John and Kara battled their diseases with cutting-edge medical treatments. Both had countless prayers lifted on their behalf. Both believed in a powerful, loving God who could heal. Yet one lived and one died. How can we accept both endings as from the hand of God? Did one person have greater favor? Deeper faith?

Un ouvrage percutant sur une femme qui se bat, une véritable source d'inspiration pour tous et toutes. Avec force détails, rires et joies, Paola Corbo nous raconte son quotidien avec la sclérose en plaques avec un détachement hors du commun. "La descente aux enfers" pourrait bien définir le parcours de Paola n'eut été l'extraordinaire prise de pouvoir de ses pensées sur son état physique. Ceci est l'histoire, écrite à trois plumes, de la vie d'un vif-argent peu à peu restreint à rouler sa bosse dans un fauteuil électrique.

These are the extraordinary realities of the NHS front line. From the historic junior doctor strikes to the 'humanitarian crisis' declared by the Red Cross, the overstretched health service is on the precipice. This is a powerful polemic on its systematic degradation and a letter of optimism to that same health service and those who support it. It captures with tenderness a new doctor's experiences of an NHS at breaking point.

The autobiography is told in an honest and very candid way, from the very first diagnosis in 2011 right up to the present day, showing how I was forced to crowdfund to have my leg amputated, what it took to overcome the struggles of four operations, and what it meant for me and my young family.

Considering herself unsuitable for any other contribution to the war effort, Monica Dickens opts for nursing, imagining herself gliding through the wards, serene in a pure white halo cap. On enrolment, however, she is promptly stripped of all illusions. Intelligent and headstrong, Monica struggles to submit to the iron rule of the Matron and toils over the mountains of menial work that are a trainee's lot. But there are friends among the staff and patients, night-time escapades to dances with dashing army men and her secret writing project to keep her going.

In 2017, David got what he thought was a mild touch of the flu. This book is the story of why David would make a lousy doctor. Contrary to the book’s title, David had lymphoma and it was terminal. But A Mild Touch of the Cancer isn’t your standard "how I survived" compendium. It is a hilarious tale, written while battling one of life’s greatest challenges. It’s a book about living with optimism and positivity, by a self-proclaimed Genetically Modified Organism.

In the midst of World War II, James is training for the Royal Air Force, while going home to Yorkshire whenever possible to see his very pregnant wife, Helen. Musing on past adventures through the dales, visiting with old friends, and introducing scores of new and amusing characters—animal and human alike—Herriot enthralls with his uncanny ability to spin a most engaging and heartfelt yarn.

In this transporting book, David Oliver Relin shines a light on the work of Geoffrey Tabin and Sanduk Ruit, gifted ophthalmologists who have dedicated their lives to restoring sight to some of the world’s most isolated, impoverished people through the Himalayan Cataract Project, an organization they founded in 1995. Tabin was the high-achieving bad boy of Harvard Medical School, an accomplished mountain climber and adrenaline junkie as brilliant as he was unconventional.

An Epidemic of Absence asks what will happen in developing countries, which, as they become more affluent, have already seen an uptick in allergic disease: Will India end up more allergic than Europe? Velasquez-Manoff also details a controversial underground movement that has coalesced around the treatment of immune-mediated disorders with parasites. Against much of his better judgment, he joins these do-it-yourselfers and reports his surprising results.

Every day when Dr. Carson went to work as a surgeon, he had to make life-and-death decisions. For that reason, and because so many of the people and families he worked with had suddenly been forced to reconsider what's really important in life, he's spent a lot of his own time searching for perspective.

Ma vie a basculé une nuit où tout semblait pourtant si calme. La bête s’est glissée dans mon corps et ne m’a plus laissé une journée de répit. Il a fallu attendre des années pour, qu’enfin, on puisse poser un nom sur cette pathologie : l’algie vasculaire de la face. Les médecins la surnomment « la maladie du suicide » et comparent l’intensité de sa douleur à une amputation sans anesthésie. Ne pouvant me résoudre à vivre avec cette douleur insoutenable, j’ai tout essayé, faisant souvent même office de cobaye.