Medical Memoirs

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.

Facing the prospect of a career-ending disability as she adjusts to life with multiple sclerosis, Dr. Lisa Doggett is forced to deal with a new level of uncertainty and vulnerability, and the everyday fear that something new will go wrong. Taking off her white coat—becoming a patient herself—she confronts unimaginable fears, copes with her limitations, and sidesteps her skepticism of alternative medicine to seek help from unlikely sources. MS pushes Doggett—a perfectionist at heart—to embrace self-compassion.

Karen Fine always knew that she wanted to be a vet and wasn't going to let anything stop her: not her allergy to cats, and not the fact that in the '80s veterinary medicine was still a mostly male profession. Inspired by her grandfather, a compassionate doctor who paid house calls to all his (human) patients, Dr. Fine persevered, and brought her Oupa's principles into her own practice, which emphasizes the need to understand her patients’ stories to provide the best possible care.

In the early 2000s, 16-year-old Todd Davison and his older brother Wade were living the Canadian hockey dream—playing together in the Western Hockey League, a stepping-stone for many future NHL stars. Todd seemed destined to be one of them. But after facing off against Sidney Crosby at the Canada Winter Games in 2003, that dream became a nightmare when Todd's mysterious shoulder pain led to a devastating cancer diagnosis. His Last Shift: The Playbook of Todd Davison recounts the journey of an incredible young man as he comes to terms with his death long before his time.

Drawing on the author’s personal experiences with both tame and wild moose, this handbook contains a wealth of information about this unique animal from all corners of the world. An overview of moose biology is featured, including their specialized diet and the relationship between sex and antlers, where size really does matter. Covering the history of moose on earth and the marked fluctuations in populations that have occurred over time, this guide also contains accessible chapters exploring moose diseases, moose and traffic, moose as a resource, and the uses of live moose in several ways, ranging from transport and clothing to dairy animals and pets.

Using the most common postmortem process as the backbone of the narrative, The Chick and the Dead takes the listener through the process of an autopsy while also describing the history and changing cultures of our relationship with the dead. The book is full of vivid insight into what happens to our bodies in the end. Each chapter considers an aspect of an autopsy alongside an aspect of Carla's own life and work and touches on some of the more controversial aspects of our feelings toward death.

Informational and positive look on the hard diagnosis. Lifting the stigma, finding that you are not alone in all this. The audiobook is a personal journey, finding what the disease is all about, managing the difficult moments of depressions and hypo-mania episodes until a stable effect is reached, the so-called remission. The author also shares her successes, talents and everything she has learned in an optimistic and positive way.

At 28, Jessica Fechtor was happily immersed in graduate school and her young marriage and thinking about starting a family. Then one day she went for a run, and an aneurysm burst in her brain. She nearly died. She lost her sense of smell and the sight in her left eye and was forced to the sidelines of the life she loved. Jessica's journey to recovery began in the kitchen as soon as she was able to stand at the stovetop and stir. There, she drew strength from the restorative power of cooking and baking.

Furiously Happy meets Elaine Lui in this truly original - and surprisingly hilarious - memoir about one woman’s journey to learn how to walk after a debilitating diagnosis turned her life upside down.Learn How to Walk (Again) To-Do List: Step 1: Stand, Step 2: Step, Step 3: Pee (Yes!), Step 4: Walk with walker, Step 5: Walk with sticks, Step 6: Walk without props Recreational interlude for sex Step, 7: RUN! Ruth Marshall - power-mom, wife, actor, and daughter - was in great health, until one day, her feet started to tingle.

Switching Time is the first story centering on multiple personality disorder to be told by the treating physician. It is the incredible saga of a young woman stranded in unimaginable darkness who, in order to survive, created 17 different versions of herself. One by one, Karen's "alters" began showing themselves: men, women, young boys, a toddler, black, white, vicious, nurturing, prim, licentious. And their "stepping out" confronted Baer with the challenge of a lifetime.

Oftentimes, psychic "gifts" don’t feel like a gift at all. In this thrilling memoir, Sarah K. Grace describes in vivid detail what it's like to be in the trenches of some of California's busiest 911 systems as both a paramedic and highly sensitive clairvoyant/empath.

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.

Danielle Perreault a neuf ans la première fois qu’elle souhaite s’expatrier: son père s’est fait offrir un poste à la nouvelle Université du Rwanda et, pour elle, c’est tout décidé : ils partent en Afrique ! Mais son père, à sa grande déception, refuse... Dix ans plus tard, toujours attirée par l’aventure, elle part enseigner au Togo. Elle reçoit un salaire de vingt dollars par mois, mais elle est logée, nourrie, et on lui fournit la mobylette. Que demander de plus?!

With a play opening on Broadway, and every reason to smile, Sarah Ruhl has just survived a high-risk pregnancy when she discovers the left side of her face is completely paralyzed. She is assured that 90 percent of Bell’s palsy patients experience a full recovery—like Ruhl’s own mother. But Sarah is in the unlucky ten percent. And for a woman, wife, mother, and artist working in theater, the paralysis and the disconnect between the interior and exterior brings significant and specific challenges.

In this searing and poignant memoir, Alex Belth and Emily J. Shapiro delve deep into their relationship history, what they brought to their marriage, and what remains. At first glance, it seems the biggest challenge they face is Emily’s chronic illness - and the impact that’s had on their life as a couple. But her medical conditions aren’t the only thing that set the relationship on a precipice. When they start to work through their issues, it prompts a closer examination of Alex and the ways his needs and personal history challenge their partnership.

At nineteen years old, Nicole C. Kear's biggest concern is choosing a major - until she walks into a doctor's office in midtown Manhattan and gets a life-changing diagnosis. She is going blind, courtesy of an eye disease called retinitis pigmentosa, and has only a decade or so before lights-out. Instead of making preparations as the doctor suggests, Kear decides to carpe diem and make the most of the vision she has left. She joins a circus school, tears through boyfriends, travels the world, and through all these high jinks, she keeps her vision loss a secret.

Into the Gray Zone takes listeners to the edge of a dazzling, humbling frontier in our understanding of the brain: the so-called "gray zone" between full consciousness and brain death. People in this middle place have sustained traumatic brain injuries or are the victims of stroke or degenerative diseases, such as Alzheimer's and Parkinson's. Many are oblivious to the outside world, and their doctors believe they are incapable of thought.

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.

Fresh out of medical residency, Dr. Benjamin Gilmer joined a rural North Carolina clinic only to find that its previous doctor shared his last name. Dr. Vince Gilmer was loved and respected by the community—right up until he strangled his ailing father and then returned to the clinic for a regular week of work. Vince’s eventual arrest for murder shocked his patients. How could their beloved doctor be capable of such violence? The deeper Benjamin looked into Vince’s case, the more he became obsessed with discovering what pushed a good man toward darkness.

In The Song of Our Scars, physician Haider Warraich offers a bold reexamination of the nature of pain, not as a simple physical sensation, but as a cultural experience. Warraich, himself a sufferer of chronic pain, considers the ways our notions of pain have been shaped not just by science but by politics and power, by whose suffering mattered and whose didn’t.