Medical Memoirs

In the novel Little Women, Mr. March goes off to war. But in real life, it was Jo March (Louisa May Alcott herself, an avowed abolitionist) who traveled to Washington to nurse Northern soldiers. This is Alcott’s memoir but she chose to use the pseudonym “Tribulation Periwinkle” to tell her story. Despite the subject matter, her account is full of amusing anecdotes as she makes her way alone from Concord, Massachusetts to DC, trying to finagle a free ticket and convinced she will drown during the journey.

At age fourteen, Laura Delano saw her first psychiatrist who immediately diagnosed her with bipolar disorder and started her on a mood stabilizer and antidepressant. At school, Delano was elected the class president and earned straight-As and a national squash ranking; at home, she unleashed all the rage and despair she felt, lashing out at her family and locking herself in her bedroom, obsessing over death. Delano’s initial diagnosis marked the beginning of a life-altering saga

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. Schooled in the latest medical technology, the eager doctor—his wife, Barb, and two-year-old daughter, Kate, in tow—is about to discover that there are some things in rural practice for which medical school just hadn’t prepared him. But he’s about to learn.

Hannah Daly is a pediatric occupational therapist and an advanced sensory integration practitioner who is profoundly dyslexic, dyspraxic, and has sensory processing disorder. She has multiple university degrees but still cannot read or write. In Knowing No Boundaries, she gives an honest account of living with these hidden disabilities. This book is a unique coming-of-age, feel-good memoir that strikes the balance of vulnerability and humor.

Hoping for the stability he needs to start a family, Sandeep Jauhar, an attending cardiologist, accepts a position at a massive teaching hospital on the outskirts of Queens. With a decade's worth of elite medical training behind him, he is eager to settle down and reap the rewards of countless sleepless nights. Instead, he is confronted with sobering truths. Doctors' morale is low and getting lower.

A doctor’s powerful and deeply human memoir about the mysteries of the brain and his 40-year quest to find a treatment for multiple sclerosis.

All Janine Urbaniak Reid ever wanted was for everyone she loved to be okay so she might relax and maybe be happy. Her life strategy was simple: do everything right. This included trying to be the perfect mother to her three kids so they would never experience the kind of pain she pretended not to feel growing up. What she didn’t expect was the chaos of an out-of-control life that begins when her young son’s hand begins to shake.

Crushed between a truck and a tree, Simon and his wife were both pronounced dead at the scene of a horrific car accident. Enduring a broken skull, jaw, arms, clavicle and pelvis, followed by a coma, Simon lives to tell his remarkable journey from tragedy to triumph.

Marty, age 57, was given a preliminary diagnosis of ALS by his family doctor. Seven weeks later, the diagnosis was confirmed by a neurologist. Ten months and ten days later, Marty passed away. From day one, Alison, Marty’s spouse of over twenty-five years, kept a journal as a way to navigate the overwhelming state of her mind and soul. Soon the rawness of her words harmonized to tell the story of Marty’s diagnosis, illness, and decline. Dance Me to the End is an evocative memoir about witnessing a loved one suffer from a neurological, degenerative, and terminal disease.

When Damon Tweedy begins medical school, he envisions a bright future where his segregated, working-class background will become largely irrelevant. Instead, he finds that he has joined a new world where race is front and center. The recipient of a scholarship designed to increase black student enrollment, Tweedy soon meets a professor who bluntly questions whether he belongs in medical school, a moment that crystallizes the challenges he will face throughout his career.

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.

From New York Times best-selling author, Emmy award-winning broadcast journalist, and leading Alzheimer's advocate Meryl Comer comes a profoundly intimate account of her husband's battle with Alzheimer's disease, one of today's most pressing - and least understood - health epidemics.

Has there ever been a time in your life when you’ve felt alone or unsure where to turn for answers? It may have come with the diagnosis of a life-threatening illness, loss of a job, a death of a loved one, or any trauma that threatened everything you knew to be true. In Unexpected: Finding Resilience through Functional Medicine, Science, and Faith, Dr. Jill Carnahan introduces a new paradigm for listeners who are going through uncertain times. For the skeptic or the faithful, Unexpected is a valuable guide for living an extraordinary life of love and resilience.

James Herriot meets Jeff Foxworthy in the real-life adventures of a traveling horse doctor. Climb into the truck alongside large animal vet Dr. Madison Seamans and race to the aid of horses with wounds, stomach aches, allergies, and bizarre behaviors, as well as those in severe physical distress. Quite by accident, you'll find yourself familiar with and understanding common equine medical problems and how they are diagnosed and treated, all while marveling at the remarkable situations a country veterinarian can find himself in.

Daniel Tammet can perform extraordinary maths in his head, sees numbers as shapes, colours, textures, and motions, and can learn to speak a language fluently from scratch in three days. He also has a compulsive need for order and routine. He eats exactly 45 grams of porridge for breakfast and cannot leave the house without counting the number of items of clothing he's wearing. If he gets stressed or unhappy, he closes his eyes and counts. But in some ways, Daniel is not all like the Rain Man.

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.

At the 16 week foetal stage, Paul Whymark’s brain development was frozen as a consequence of the drug, Thalidomide. His journey is one of considerable self discovery, but also reveals greater societal insights. “16 Weeks and Everything After...” uncovers the remarkable fact that over the last 50-60 years the establishment has failed to genuinely independently review Thalidomide, and as a consequence, harms on developing life continue to have the potential to occur into the future.

ALS is a deadly disease that didn't want to let go of me. I went from hope to planning my own death as a way of escaping this demon. My journey is a view into the life of a person who needs 24-hour care, never any privacy. I was given 18 months to get my affairs in order. That lead me to seeking a higher power than the doctors. I have never witnessed an energy healing until it happened to me. This book is my call to each of you and your family who are challenged by ALS. My frame of mind was my only power.

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.

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.