Medical Memoirs

In this award-winning memoir, two sisters reckon with the convalescence and death of their outlandishly tyrannical mother and the care of their psychologically terrorized father, all relayed with dark humor and brutal honesty.

"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."

Ken Holmes worked in the Marin County Coroner's Office for 36 years, starting as a death investigator and ending as the three-term, elected coroner. As he grew into the job - which is different from what is depicted on television - Holmes learned a variety of skills, from finding hidden clues at death scenes, interviewing witnesses effectively, managing bystanders and reporters, preparing testimony for court, to notifying families of a death with sensitivity and compassion.

En France, on tue tous les jours, toutes les heures. Les faits divers envahissent les journaux, les séries télévisées de médecine légale prolifèrent, les histoires criminelles, réelles ou fictives, exercent sur le public une fascination sans borne. Michel Sapanet est médecin légiste. Sa vie, c'est la mort. Sur sa table en inox, avec un immense respect, il pratique son autopsie: exploration des boîtes crâniennes, inspection des chairs meurtries, ouverture des cœurs. Égorgés, poignardés, étranglés, pendus, tués par balle, toutes les victimes finissent par parler.

An exquisite memoir about how to live - and love - every day with "death in the room", from poet Nina Riggs, mother of two young sons and the direct descendant of Ralph Waldo Emerson, in the tradition of When Breath Becomes Air.

A mesmerizing and courageous memoir: the story of two sisters uncovering the depth of their love through the life-and-death experience of a bone marrow transplant. Throughout her life Elizabeth Lesser has sought understanding about what it means to be true to yourself and, at the same time, truly connected to the ones you love. But when her sister, Maggie, needs a bone marrow transplant to save her life, and Lesser learns that she is the perfect match, she faces a far more immediate and complex question about what it really means to love.

In early 2011, Yolanda Hadid was struck by mysterious symptoms including brain fog, severe exhaustion, migraines, and more. Over the months and years that followed, she went from being an outspoken, multitasking, hands-on mother of three, reality TV star, and social butterfly to a woman who spent most of her time in bed. Yolanda was turned inside out by some of the country's top hospitals and doctors, but due to the lack of definitive diagnostic testing, she landed in a dark maze of conflicting medical opinions.

Kristine Barnett’s son Jacob has an IQ higher than Einstein’s, a photographic memory, and he taught himself calculus in two weeks. At 9 he started working on an original theory in astrophysics that experts believe may someday put him in line for a Nobel Prize, and at age 12 he became a paid researcher in quantum physics. But the story of Kristine’s journey with Jake is all the more remarkable because his extraordinary mind was almost lost to autism. At age 2, when Jake was diagnosed, Kristine was told he might never be able to tie his own shoes.

From Darkness to Sight chronicles the remarkable life journey of Dr. Ming Wang, a world-renowned laser eye surgeon and philanthropist. As a teenager, Ming fought valiantly to escape one of history’s darkest eras - China’s Cultural Revolution - during which millions of innocent youth were deported to remote areas to face a life sentence of poverty and hard labor. Through his own tenacity and his parents’ tireless efforts to provide a chance of freedom for their son, Ming eventually made his way to America with $50 in his pocket and an American dream in his heart.

In 1953, a 27-year-old factory worker named Henry Molaison - who suffered from severe epilepsy - received a radical new version of the then-common lobotomy, targeting the most mysterious structures in the brain. The operation failed to eliminate Henry’s seizures, but it did have an unintended effect: Henry was left profoundly amnesic, unable to create long-term memories. Over the next 60 years, Patient H.M., as Henry was known, became the most studied individual in the history of neuroscience, a human guinea pig who would teach us much of what we know about memory today.

My editor had ok'd the story, "The Unveiling of a Quack", and now I faced the man whom the power of the press would squash like a bug. "Five times," he said quietly in response to my question, "the Medical Society of the County of New York sent a committee here to investigate my methods. I let them see patients, X-rays, records, everything." "And what were the results of those investigations?"

At twenty-six, Gaby felt like her life was just beginning. Newly married and pregnant with her first child, she was on top of the world. But that joy was shattered when a routine blood test led to a diagnosis of AML Leukemia—and the treatment she needed could harm her baby or save them both.

Blinded at age three, Mike May defied expectations by breaking world records in downhill speed skiing, joining the CIA, and becoming a successful inventor, entrepreneur, and family man. He had never yearned for vision. Then, in 1999, a chance encounter brought startling news: a revolutionary stem-cell transplant surgery could restore May's vision.

Dr. Lange graduated from medical school in 1981, right as a new plague swept across the globe. His story became intertwined with the story of HIV. At once a physician, scientist, AIDS activist, and medical diplomat, Lange studied ways to battle HIV and prevent its spread from mother to child. Fighting the injustices of poverty, Lange advocated for better access to health care for the poor and the vulnerable. The Impatient Dr. Lange is the story of one man's struggle against a global pandemic - and the tragic attack that may have slowed down the search for a cure.

A leading oncologist at the University of California-San Francisco, Dr. Pamela Munster has advised thousands of women on how to deal with the life-altering diagnosis of breast cancer. But when she got a call saying that her own mammogram showed "irregularities", she found herself experiencing a whole new side of the disease she thought she was an expert in. Weaving together her personal story with her team's groundbreaking research on the BRCA gene, Twisting Fate is an inspiring guide to living with BRCA mutations.

Lene Fogelberg is dying - she is sure of it - but no doctor in Sweden, her home country, believes her. Love stories enfold her, with her husband, her two precious daughters, her enchanting surroundings, but the question she has carried in her heart since childhood - will I die young? - is threatening all she holds dear, even her sanity. When her young family moves to the US, an answer, a diagnosis, is finally found: She is in the last stages of a fatal congenital heart disease. But is it too late?

Dr Dave Walker was a successful anesthesiologist with a special interest in the intensive care unit (ICU). Disillusioned with God after a series of tragedies, he was living for himself and his work. Yet he longed for more than just physical healing for his patients, which set him on a quest to find a God who cared. After a dramatic encounter, he started praying with his patients.

By the age of 13, Lily Bailey was convinced she was bad. She had killed someone with a thought, spread untold disease, and ogled the bodies of other children. Only by performing an exhausting series of secret routines could she make up for what she'd done. But no matter how intricate or repetitive, no act of penance was ever enough. Beautifully written and astonishingly intimate, Because We Are Bad recounts a childhood consumed by obsessive compulsive disorder.

Patti Davis, the daughter of Ronald and Nancy Reagan, writes about losing her father to Alzheimer's disease, saying goodbye in stages, and watching the progression of a disease that steals what is most precious: a person's memory. Past and present come together in this illuminating portrait of grief, of a man, a disease, and a girl and her father.

In this powerful, wide-ranging, and emotional story about the limits of medical knowledge, Abel discovers why she wasn't diagnosed with celiac as a child. She considers how environmental fears and Internet anecdotes lead people to avoid gluten. And she grapples with the question that confronts us all: how to live calmly, even joyfully, in the face of uncertainty.