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The searing intimacy of Girl, Interrupted combined with the uncomfortable truths of The Empathy Exams in a collection of essays chronicling one woman’s experiences as both patient and caregiver, giving a unique perspective from both sides of the hospital bed.

Los amarillos son las personas que dan sentido a nuestra vida que se sitúan entre el amor y la amistad. El mundo amarillo es un mundo fantástico que quiero compartir contigo. Es el mundo de los descubrimientos que hice durante los diez años que estuve enfermo de cáncer. Es curioso, pero la fuerza, la vitalidad y los hallazgos que haces cuando estás enfermo sirven también cuando estás bien, en el día a día.Este audiolibro pretende que conozcas y entres en este mundo especial y diferente; pero, sobre todo, que descubras a los “amarillos”.

“Discharged from a hospital just means you’re not dead.” These words of Ralph B. Lilly, M.D., describe his early struggle to recover from a traumatic brain injury. Lilly was a forty-four-year-old practicing neurologist sitting on his motorcycle at a red light when a drunk driver rear-ended him in 1980. In the ICU, after regaining consciousness and being told what happened, he asked, “What’s a hospital? What’s a motorcycle?” This tragic experience transformed his life and his approach to his neurology practice: doctors treat those with brain injury; but loved ones heal them.

Have you ever wondered what it's like to save a life? In his book Life Changing Paramedic Stories, Dion talks about 12 life-changing experiences while working as a Canadian paramedic.

Dr. Schechter was Dr. John Sarno's first medical doctor trainee. Dr. Sarno was Schechter's most important career mentor. Schechter took an interest in TMS as a medical student, was successfully diagnosed and treated by Dr. Sarno, and did a research study in his office suite beside Dr. Sarno. With a relationship (student, professional collegial, finally fond friend) that spanned decades, Schechter reflects on Dr. Sarno's teachings in Twelve Chapters and Eighteen Lessons. Readers have noted "intimate and humanizing vignettes", "book captures Sarno's immense contributions", "rare and ...

Christine Bryden was a top civil servant and single mother of three children when she was diagnosed with dementia at the age of 46. Since then she has gone on to challenge almost every stereotype of people with dementia. This is a vivid account of the author's experiences of living with dementia, exploring the effects of memory problems, loss of independence, difficulties in communication and the exhaustion of coping with simple tasks. She describes how, with the support of her husband, Paul, she continues to lead an active life and explains how professionals and carers can help.

At 49 years old, Carol Clupny was an active, driven woman with a career, a family, and a zest for adventure. A mere year later, she struggles with strange symptoms of internal tremors, frozen shoulders, and a serious intestinal infection. She doesn’t understand why she can’t paddle a kayak or throw the ball for her dogs. Then comes the diagnosis: early onset Parkinson’s Disease. Carol is not afraid to face the apathy and depression. Instead of being drug down into darkness, she finds strategies for lifting herself, and others around her, up into the light.

In the early evening on October 1, 2003, Christina Crosby was three miles into a 17 mile bicycle ride, intent on reaching her goal of 1,000 miles for the riding season. She was a respected senior professor of English who had celebrated her 50th birthday a month before. As she crested a hill, she caught a branch in the spokes of her bicycle, which instantly pitched her to the pavement. Her chin took the full force of the blow, and her head snapped back. In that instant, she was paralyzed.

The little mountain hamlet of Bryson City, North Carolina, offers more than dazzling vistas. For Walt Larimore, a young "flatlander" physician setting up his first practice, the town presents its peculiar challenges as well. With the winsomeness of a James Herriott book, Bryson City Tales sweeps you into a world of colorful characters, the texture of Smoky Mountain life, and the warmth, humor, quirks, and struggles of a small country town.

Acclaimed CBS News reporter Barry Petersen writes about hearing the unimaginable; what it meant, what it still means, what he did---and didn't do---and how this beautiful love story needs to be heard by the thousands of families who have already heard that same devastating diagnosis: early onset Alzheimer's disease. Even though Barry has spent his long-time, award-winning television career covering wars and events that shaped the world, he was not even slightly prepared for what happened to his darling wife, Jan, and how it would impact his life.

On a family vacation in 2009, Dr. Renée Brown Harmon felt the first jolt of fear that something might be wrong. How could her husband, Harvey, a highly intelligent physician, marathon runner, and devoted father, be struggling to keep up with their guide’s simple instructions or unable to do simple math to calculate their daughter’s age? The heartbreaking truth was confirmed nine months later when he was diagnosed with younger-onset Alzheimer’s disease at age fifty.

Leaving a life marked by crippling setbacks and his father's doubt, in 1967 a 20-something doctor from India arrived in America with only five dollars and the desire to claim his American dream. Faced with an entirely new culture, racism, and the lasting effects of disabling childhood injuries, through hard work and perseverance he overcame all odds. Now having performed over 15,000 open-heart surgeries, more than nearly every surgeon in history, Dr. Singh reflects on his most memorable patients and his incredible personal life.

This is the extraordinary story of the South African boy whose bravery and fierce determination to make a difference despite being born with AIDS has made him the human symbol of the world's fight against the disease, told by the veteran American journalist whose life he changed.

When former New York Times journalist Dan Koeppel texted his cousin Robert Meyer, a 20-year veteran of the emergency room at Montefiore Medical Center in the Bronx, at the beginning of the COVID-19 crisis in the United States, he expected to hear that things were hectic. On a scale of 1 to 10, 10 being overwhelmed, where do you think you are? Koeppel asked. Meyer’s grave reply - 100 - was merely the cusp of the crisis that would soon touch every part of the globe.

Where Night Is Day is a nonfiction narrative grounded in the day-by-day, hour-by-hour rhythms of an ICU, in a teaching hospital, in the heart of New Mexico. It is the story of patients and families, suddenly faced with critical illness. In this context, Kelly reflects on the nature of medicine and nursing, on how doctors and nurses see themselves. Drawing on the words of medical historians, doctor-writers, and nursing scholars, Kelly examines the relationship of professional and lay observers, to the meaning of illness, empathy, caring, and the silence of suffering.

As an adult, National Public Radio foreign correspondent Jacki Lyden has spent her life on the front lines of some of the world's most dangerous war zones. As a child, she lived in a war zone of a different kind. Her mother, Dolores, suffered from what is now called manic depression. In her manic phases, Dolores became Marie Antoinette or the Queen of Sheba, exotically delusional, yet to young Jacki also transcendent, even inspiring. In time, Jacki grew to accept, even relish, Dolores' bizarre episodes, marveling at her mother's creative energy and using it to fuel her own.

Death was conspicuously absent during Rachel's medical training. Instead, her education focused entirely on learning to save lives, and was left wanting when it came to helping patients and their families face death. She came to specialize in palliative medicine because it is the one specialty in which the quality, not quantity of life truly matters. In the same year she started to work in a hospice, Rachel was forced to face tragedy in her own life when her father was diagnosed with terminal cancer.

The Chopra brothers were among the most eager and ambitious of the new generation. In the 1970s, they each emigrated to the United States to make a new life. Both faced tough obstacles: while Deepak encountered resistance from Western-trained doctors over what he called the mind-body connection, Sanjiv struggled to reconcile the beliefs of his birthplace with those of his new home. Eventually, each brother became convinced that America was the right place to build a life, and the Chopras went on to great achievements.

Due to horrible physical deformities, he spent much of his life as a fairground freak. He was hounded, persecuted, and starving, until his fortune changed and he was rescued, housed, and fed by the distinguished surgeon, Frederick Treves. The subject of several books, a Broadway hit, and a film, Joseph Merrick has become part of popular mythology. Here, in this fully revised edition containing much fresh information, are the true and un-romanticized facts of his life.

When Joselin Linder was in her 20s, 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 could think of - her father's.