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In the early days of the Cold War, a spirit of desperate scientific rivalry birthed a different kind of space race: not the race to outer space that we all know, but a race to master the inner space of the human body. While surgeons on either side of the Iron Curtain competed to become the first to transplant organs like the kidney and heart, a young American neurosurgeon had an even more ambitious thought: Why not transplant the brain?

When 24-year-old Susannah Cahalan woke up alone in a hospital room, strapped to her bed and unable to move or speak, she had no memory of how she’d gotten there. Days earlier, she had been on the threshold of a new, adult life: At the beginning of her first serious relationship and a promising career at a major New York newspaper. Now she was labeled violent, psychotic, a flight risk. What happened?

As a palliative care nurse, it is Kelly Critcher's job to look death in the eye - to save a patient while the fight can still be won and confront death with grace and kindness when it can't. In early 2020, everything changed for nurses on the NHS frontline. Working on Covid wards and the High Dependency Unit, Kelly spent the height of the coronavirus crisis at Northwick Park Hospital - perhaps the UK hospital most deeply ravaged by the illness.

Lysa has been a paramedic for over 20 years, working for the London Ambulance service - the world's biggest and busiest free service - for much of that time. Here, she reveals what it's really like to work in a job that brings paramedic teams face-to-face with death - and destiny - every day.

Welcome to the life of Dr Max Skittle. Therapist, relationship counsellor, social worker, friend, parent-figure - and, yes: doctor. Join Max - and his patients - as he takes us on a rollercoaster journey through a year in the life of a doctor: from infected toenails, to wonky elbows, to erectile disfunction, to bed bugs; the happy couple expecting a surprise new baby; the teenage girl struggling with body image issues; the loving family grappling with grief, Max shows us all the highs and crushing lows that come with being a GP.

When James Cook's daughter was nearly one, he began to suspect that she wasn't simply a 'late bloomer', as he and his wife were telling friends and family. Emily was strongly taken by images and patterns around the house, had a marked response to music, but never pointed at anything, and hadn't crawled yet. At the age of two-and-a-half, after months of invasive tests, Emily was finally diagnosed with severe autism and everything changed.

Being diagnosed with cancer is frightening; learning that the cancer is late stage takes that fear to unknown depths. After a year of brutal treatment, Mo Haque heard the dreaded words, 'There is nothing else we can do for you.' His cancer was terminal and left him questioning the price we put on life. Three years on from the 'small chance' of survival the experts had given him, Mo shares his incredible story: of despair and suffering, of hope and healing, of vulnerability and authenticity. This audiobook is for anyone going through the most challenging of times.

After a 25-year break from boating, Brian Harvey circumnavigates Vancouver Island with his wife, his dog, and a box of documents that surfaced after his father’s death. In this memoir, Brian Harvey shares his experience of voyaging with his father’s ghost for two months in the Pacific.

Freedom 55? The so-called “Golden Years”? What if you are slowly losing your memories and your motor skills? Or what if you are the devastated witness as your partner struggles with dementia? Lewy Body Disease is a form of dementia second only to Alzheimer’s in numbers, yet many doctors and almost no lay people have ever heard its name. This is the story of two courageous people, Julie and Ken Sobol, life partners as well as writing partners. Caught up in the frightening and fatal fog of Lewy Body Disease, they started writing this book together.

Manjusha Pawagi, a successful family court judge, has written a not-so-typical memoir about her experience with cancer. Wryly funny and stubbornly hopeful, this is her quirky take on what it’s like to face your own mortality when, to be honest, you thought you’d live forever. She describes how even the darkest moments of life can be made worse with roommates; details how much determination it takes to ignore the statistics; and answers the age-old question: What does it take to get a banana popsicle around here?

From Ethiopia to Sierra Leone, Tanzania to Togo, Dr Andrew Browning has been helping women affected by obstetric fistulas - a debilitating condition resulting from obstructed childbirth - for nearly two decades. Andrew began his African career in the 1990s working with the late Dr Catherine Hamlin and since then has started the Barbara May Foundation, which has built hospitals, trained staff and established programs to heal fistulas and also prevent them from occurring around Africa in the world's most disadvantaged women.

Two incredible women, an unlikely friendship and a united mission to save the lives of some of the world's poorest and most desperate women. Healing Lives reveals the untold tale of Mamitu Gashe, Dr Catherine Hamlin's protégée, and the inspiring almost 60-year friendship between the two women. In 1962, three years after Drs Catherine and Reg Hamlin arrived in Ethiopia, an illiterate peasant girl sought their aid. Mamitu Gashe was close to death and horrifically injured during childbirth after an arranged marriage in a remote mountain village.

Lorena Junco Margain - passionate art collector and devoted wife and mother - is already shaken after abruptly fleeing Mexico and relocating in the USA with her family while pregnant due concerns for their safety. Then, she learns she has a tumor on her adrenal gland. Rather than improve after surgery, her condition worsens. On the Way to Casa Lotus is the gripping true story of Junco Margain’s journey coming to terms with the permanent consequences of a surgeon’s devastating mistake.

When her six-year-old daughter found her collapsed on the kitchen floor, Rachel had no idea how much her life was about to change. A brain scan revealed a dark shadowy mass, a huge abnormal growth of tissue that, whilst benign, was still growing and would surely kill her. It was too big to operate on. It needed to be "managed", and Rachel had, at best, two years to live. Refusing to accept the bleak prognosis, Rachel was determined to stay alive.

Cystic fibrosis was once a mysterious disease that killed infants and children. Now it could be the key to healing millions with genetic diseases of every type - from Alzheimer's and Parkinson's to diabetes and sickle cell anemia. Told from the perspectives of the patients, families, physicians, scientists, and philanthropists fighting on the front lines, Breath from Salt is a remarkable story of unlikely scientific and medical firsts, of setbacks and successes, and of people who refused to give up hope....

In April 2014, Deputy Editorial Director at BuzzFeed Lara Parker opened up to the world in an article on the website: She suffers from endometriosis. And beyond that? She let the whole world know that she wasn’t having any sex, as sex was excruciatingly painful. Less than a year before, she received not only the diagnosis of endometriosis, but also a diagnosis of pelvic floor dysfunction, vulvodynia, vaginismus, and vulvar vestibulitis.

In ADHD and Me, he tells about the next 12 years as he learns to live with both the good and bad sides of life with ADHD. Blake's memoir offers, for the first time, a young person's account of what it's like to live and grow up with this common condition. Join Blake as he foils bullies, confronts unfair teachers, struggles with distraction and disorganization on exams, and goes sailing out-of-bounds and ends up with a boatload of spiders.

Army combat veteran and registered nurse Erin Olszewski's most deeply held values were put to the test when she arrived as a travel nurse at Elmhurst Hospital in the epicenter of the COVID-19 pandemic. After serving in Iraq, she was back on the front lines - and this time, she found, the situation was even worse. Rooms were filthy, nurses were lax with sanitation measures, and hospital-acquired cases of COVID-19 were spreading like wildfire.

In his early 20s, Mindy Greiling's son, Jim, was diagnosed with schizoaffective disorder after experiencing delusions that demanded he kill his mother. At the time, and for more than a decade after, Greiling was a Minnesota state legislator who struggled, along with her husband, to navigate and improve the state's inadequate mental health system. Fix What You Can is an illuminating and frank account of caring for a person with a mental illness, told by a parent and advocate.

At the age of 53, Tony walks away from a life of journalism and into an unknown future dogged by self-doubt and financial worry. June is 48 years old then, a writer and a teacher, and over the following nine years she watches as her husband gradually changes - in interests, goals, and behavior - until Tony has a sudden fall, ending their life as they have known it.