Próximamente

Little Miss Diagnosed has descriptive copy which is not yet available from the Publisher.

The Casino Shift has descriptive copy which is not yet available from the Publisher.

In Sickness and in Health has descriptive copy which is not yet available from the Publisher.

Pieces You’ll Never Get Back is a harrowing and redemptive memoir, in which a new mother must reconstruct her shattered mind, her relationship to her religious upbringing, and her life’s purpose.

Paranormal begins with a harrowing account of Moody’s suicide attempt—due to an undiagnosed illness that led him into depression—and proceeds to explore his lifelong fascination with life beyond our bodies. Moody traces the roots of his obsession with the point of death and how, at age twenty-three, he launched the entirely new medical field of near-death studies. He went on to explore the world of past lives and possible reincarnation before stumbling into the fascinating realm of facilitated visions.

At age thirty-eight, Jonathan Gluck, a new father with a promising journalism career, was shocked to learn he had multiple myeloma, a rare, incurable blood cancer. He was told he had eighteen months to live. That was more than twenty years ago. Gluck isn’t just something of a medical miracle. He’s also part of a growing population. Thanks to revolutionary medical advances, many cancers and other serious illnesses are no longer death sentences but chronic diseases people can often live with for years.

A girl believes she has been struck blind for stealing a kiss. A mother watches helplessly as each of her children is replaced by a changeling. A woman is haunted each month by the same four chords of a single song. In neurology, illness is inextricably linked with narrative, the clues to unraveling these mysteries hidden in both the details of a patient's story and the tells of their body.

For fifteen years, Joanna Sokol filled private notebooks with her confusion, humor, and anger about the strange world of American street medicine. As her career progressed, she found herself taking notes on scraps of paper, backs of gloves, and margins of EKG printouts. She read about the history that brought ambulances into their current role as the caretakers of society’s forgotten, and spoke to her colleagues about their own experiences and perspectives. Those reflections are collected here, in a series of raw, powerful essays about the state of American medicine.

For the many millions of headache sufferers and fans of Mary Roach, Siddartha Mukerjee, and Ed Yong, a deeply reported, sometimes harrowing, and frequently humorous journey into the author’s own excruciating headaches, and the science behind these surprisingly mysterious disorders that may, finally, offer relief.

In the 1950s, the field of psychiatry had nothing to show for itself. While polio was being cured, antibiotics were being discovered, and cancer research was developing, the mental health world had no wins. Asylums were full and nobody had figured out how to fix insanity—specifically schizophrenia, the severest mental illness. Scientists became convinced that if they could engineer a pill to create madness, then they could cure it.

Tiffany Graham Charkosky was eleven years old when her mother, Julie, died. Eighteen years later, she discovers that the genetic mutation that took her mother has been passed down to Tiffany herself. But with this devastating news, Tiffany finds a certain strength in hope, resilience, and knowledge. She will fight for her family’s future.

In the final stretch of his doctoral internship, Dr. Jonathan Mathias Lassiter had just one more milestone to complete: the diversity project, where candidates insert themselves into a situation in which they'd experience what it’s like to be a minority and then share their experience with the class. Surprisingly, the all-white training committee failed him! They concluded that the program’s first and only Black intern did not understand diversity. Frustrated and panicked, he thought: “These white people are crazy."

Neuroscientist Lipska was diagnosed early in 2015 with metastatic melanoma in her brain's frontal lobe. As the cancer progressed and was treated, she experienced behavioral and cognitive symptoms connected to a range of mental disorders, including dementia and her professional specialty, schizophrenia. Lipska's family and associates were alarmed by the changes in her behavior, which she failed to acknowledge herself.

Surviving Paris has descriptive copy which is not yet available from the Publisher.

Shahd Alshammari is just eighteen when she is diagnosed with multiple sclerosis, and told by her neurologist that she would not make it past age thirty. Despite what she is told, by thirty, she has become a professor of literature, and has managed to navigate education systems in both Kuwait and the United Kingdom and inspire generations of students. Head above Water is the intimate, philosophical memoir of Shahd Alshammari's life of triumph and resistance, as a woman marked "ill" by society and as a lifelong reader, student, and teacher.

In No Woman Left Behind, Grant recounts her decision to abandon a promising advertising career, and the ups and downs of building Silicon Valley–based Fistula Foundation from a modest start-up into the global leader in fistula treatment. Through vivid firsthand accounts of surgeons toiling in remote corners of Africa and Asia, we see inside the fight to restore hope to some of the world’s most vulnerable women.

When paramedic Tim Booth finds himself rushing a patient's dead cat to a (human) hospital's Emergency Department for resuscitation, he finds himself wondering where it all went wrong. From bedroom mishaps and hypochondriacs to suspicious rashes and freak cattle incidents, the doctors, nurses and paramedics of our hospital EDs have seen everything. Every day, Tim and his colleagues battle burnout, an overburdened healthcare system and compassion fatigue, powered only by caffeine, dark humour and a heartfelt drive to save lives.

An estimated tens of millions of Americans live with conditions that elude diagnosis, often navigating a healthcare system that fails to recognize or effectively address their suffering. Journalist Alexandra Sifferlin has spent years investigating the diagnosis crisis in America—what it means to live without a diagnosis and how both medical and patient communities are working to improve the diagnostic process.

When Vida is born to Mina and husband Freddie, it is love at first sight. She is perfect. But it is also clear from early on that something is not right. This is the story of how Vida came to be diagnosed with rare blood disorder Diamond Blackfan Anaemia, and how Mina and her family’s lives were transformed by the experience of having a child with such a serious condition. Together, they move with fierce tenacity into a future that Mina never expected, but one that is rich with love, hope and community.

From the remarkable man whose life inspired the heartstopping film, ‘I Swear’, a book that offers extraordinary insight into what it’s like to live with a severe form of Tourette’s Syndrome: a fascinating, complex condition that’s more common than most of us think (1 in 100 schoolchildren have the condition), and yet is chronically misunderstood.