LOS ANGELES TIMES AND PUBLISHERS WEEKLY BESTSELLER • The powerful memoir of a young doctor and former college athlete diagnosed with a rare disease who spearheaded the search for a cure—and became a champion for a new approach to medical research. “A wonderful and moving chronicle of a doctor’s relentless pursuit, this book serves both patients and physicians in demystifying the science that lies behind medicine.”—Siddhartha Mukherjee, New York Times bestselling author of The Emperor of All Maladies and The Gene David Fajgenbaum, a former Georgetown quarterback, was nicknamed the Beast in medical school, where he was also known for his unmatched mental stamina. But things changed dramatically when he began suffering from inexplicable fatigue. In a matter of weeks, his organs were failing and he was read his last rites. Doctors were baffled by his condition, which they had yet to even diagnose. Floating in and out of consciousness, Fajgenbaum prayed for a second chance, the equivalent of a dramatic play to second the game into overtime. Miraculously, Fajgenbaum survived—only to endure repeated near-death relapses from what would eventually be identified as a form of Castleman disease, an extremely deadly and rare condition that acts like a cross between cancer and an autoimmune disorder. When he relapsed while on the only drug in development and realized that the medical community was unlikely to make progress in time to save his life, Fajgenbaum turned his desperate hope for a cure into concrete action: Between hospitalizations he studied his own charts and tested his own blood samples, looking for clues that could unlock a new treatment. With the help of family, friends, and mentors, he also reached out to other Castleman disease patients and physicians, and eventually came up with an ambitious plan to crowdsource the most promising research questions and recruit world-class researchers to tackle them. Instead of waiting for the scientific stars to align, he would attempt to align them himself. More than five years later and now married to his college sweetheart, Fajgenbaum has seen his hard work pay off: A treatment he identified has induced a tentative remission and his novel approach to collaborative scientific inquiry has become a blueprint for advancing rare disease research. His incredible story demonstrates the potency of hope, and what can happen when the forces of determination, love, family, faith, and serendipity collide. Praise for Chasing My Cure “A page-turning chronicle of living, nearly dying, and discovering what it really means to be invincible in hope.”—Angela Duckworth, #1 New York Times bestselling author of Grit “[A] remarkable memoir . . . Fajgenbaum writes lucidly and movingly . . . Fajgenbaum’s stirring account of his illness will inspire readers.”—Publishers Weekly

LILLY STONE is a twelve year old medical prodigy who takes after her father and uses every opportunity to learn more about the world of medicine. Desperate to treat patients of her own, Lilly meets Andre on her way home from school and finds the opportunity she has longed for. Noticing that Andre had more than a minor injury, and a family who didn't trust doctors, Lilly works to bridge the gap and treat the boy while searching for the root cause of his poor health. Chasing A Cure - that's Lilly Stone's dream. GREG PLAYER IS A DEDICATED FAMILY PHYSICIAN IN WILMINGTON, NORTH CAROLINA. HAVING TREATED PATIENTS FOR OVER TWENTY YEARS, INCLUDING HUNDREDS OF DIABETIC PATIENTS, DR. PLAYER FINDS A PARTICULAR INTEREST IN THE DOCTOR AND PATIENT RELATIONSHIP. HE APPRECIATES THE SCIENCE AND ART OF MEDICINE, AND IS EXCITED TO SHARE THE MEDICAL WORLD WITH YOUNG READERS EVERYWHERE.

This is a story about a woman who, in the prime of her life, is diagnosed with an autoimmune disease called scleroderma. Doris, an upbeat and optimistic person, always looked on the bright side of life. That was about to change. A strange and mysterious disease was waiting to wreak havoc with her life. Nothing prepared her for this life-altering experience. Follow her courageous journey in dealing with an autoimmune disease and sifting through the maze of doctors and treatments.

An 1865 report on public health in New York painted a grim picture of "high brick blocks and closely-packed houses . . . literally hives of sickness" propagating epidemics of cholera, smallpox, typhoid, typhus, and yellow fever, which swept through the whole city. In this stimulating collection of essays, nine historians of American medicine explore New York's responses to its public health crises from colonial times to the present. The essays illustrate the relationship between the disease environment of New York and changes in housing, population, social conditions, and the success of medical science, linking such factors to New York's experiences with smallpox, polio, and AIDS. The volume is essential reading for anyone interested in American public health and the social history of New York. The contributors are Ronald Bayer, Elizabeth Blackmar, Gretchen A. Condran, Elizabeth Fee, Daniel M. Fox, Evelynn M. Hammonds, Alan M. Kraut, Judith Walzer Leavitt, and Naomi Rogers. David Rosner is a professor of history at Baruch College and The Graduate School of the City University of New York. Robert R. Macdonald is the director of the Museum of the City of New York. A publication of the Museum of the City of New York Choice Reviews 1995 November This is one of a series of books focusing on the impact of disease intended to enhance the understanding of both past and present regarding reactions to periodic epidemics. Robert B. Macdonald, director of the Museum of the City of New York, which supports this series, states: "The individual and collective responses to widespread sickness are mirrors to the cultural, religious, economic, political, and social histories of cities and nations." Rosner selected eight renowned and respected individuals to describe the reactions and responses to smallpox, polio, and AIDS epidemics in New York City since 1860, and the efforts of officials and professionals to deal with the impact of disease. Essayists present disease broadly from economic, social, political, and health perspectives. Causes of epidemics include the expected and usual: thousands of immigrants pouring into the city, inadequate water and food supplies, lack of sewage disposal, unemployment leading to poverty. An unexpected cause was the avarice of real estate investors, inexorably driving up housing costs. Highly recommended for all students of history, public health, health policy, and sociology. Upper-division undergraduate through professional. Copyright 1999 American Library Association

A compelling exploration of the mysteries of environmental toxicity and the community of “sensitives”—people with powerful, puzzling symptoms resulting from exposure to chemicals, fragrances, and cell phone signals, that have no effect on “normals.” They call themselves “sensitives.” Over fifty million Americans endure a mysterious environmental illness that renders them allergic to chemicals. Innocuous staples from deodorant to garbage bags wreak havoc on sensitives. For them, the enemy is modernity itself. No one is born with EI. It often starts with a single toxic exposure. Then the symptoms hit: extreme fatigue, brain fog, muscle aches, inability to tolerate certain foods. With over 85,000 chemicals in the environment, danger lurks around every corner. Largely ignored by the medical establishment and dismissed by family and friends, sensitives often resort to odd ersatz remedies, like lining their walls with aluminum foil or hanging mail on a clothesline for days so it can “off-gas” before they open it. Broudy encounters Brian Welsh, a prominent figure in the EI community, and quickly becomes fascinated by his plight. When Brian goes missing, Broudy travels with James, an eager, trusting sensitive to find Brian, investigate this disease, and delve into the intricate, ardent subculture that surrounds it. Their destination: Snowflake, the capital of the EI world. Located in eastern Arizona, it is a haven where sensitives can live openly without fear of toxins or the judgment of insensitive “normals.” While Broudy’s book is wry, pacey, and down-to-earth, it also dives deeply into compelling corners of medical and American history. He finds telling parallels between sensitives and their cultural forebears, from the Puritans to those refugees and dreamers who settled the West. Ousted from mainstream society, these latter-day exiles nonetheless shed bright light on the anxious, noxious world we all inhabit now.

This book is the third in a series that focuses on teaching those with chronic pain conditions to self-manage their condition by learning the complicated process of partnering with their illness. The most important aspect of self-management with any chronic illness is acceptance and attitude because a cure is almost always unrealistic. Acceptance is the first step on the journey to wellness and helps one learn to stop being a victim to their illness and to enhance the skills necessary to achieve wellness such as effective coping, increasing resilience, and the use of positive psychology interventions. Acceptance involves coming to terms with your illness and accepting it in full followed by adjusting your attitude in the face of chronic symptoms, making you a champion of your condition.It is my belief that many illnesses that have a chronic pain component are the end result of a genetic predisposition combined with an environmental trigger and further exacerbated by our lifestyle. This trigger may come in many forms commonly reported as a trauma; exposure to toxins, bacteria, and viruses; and long-term emotional distress but may also be present from poor lifestyle choices such as a lifetime of poor diet, the lack of exercise, and too much stress--things we can manage ourselves but often fail to do so. There remains a burgeoning interest in how the psychology controls the biology, including our positive affect and our resilience. Ergo, we can't cure chronic illness, so we learn to partner with it.The reality is that with chronic pain conditions, we the patient have to learn to manage our chronic illness to the best of our ability using Western medicine as an adjunct, and this involves the use of positive psychology and complementary and alternative medicine interventions. We stop asking questions we are likely not to find the answers to and we accept that the cure then lies in our ability to champion our wellness and reverse many of our symptoms. This book takes you through the evolution of illness to wellness--from the beginning of dealing with a complicated and disabling force to the many steps of acceptance, coping, nutrition, exercise, loss, the psychology of chronic illness, and finding hope when there is none. Chronic illness does not have to translate into a poor quality of life if you don't let it. Beyond that, the goal is to learn to live life with disease.

“Disability rights activist Alice Wong brings tough conversations to the forefront of society with this anthology. It sheds light on the experience of life as an individual with disabilities, as told by none other than authors with these life experiences. It's an eye-opening collection that readers will revisit time and time again.” —Chicago Tribune One in five people in the United States lives with a disability. Some disabilities are visible, others less apparent—but all are underrepresented in media and popular culture. Activist Alice Wong brings together this urgent, galvanizing collection of contemporary essays by disabled people, just in time for the thirtieth anniversary of the Americans with Disabilities Act, From Harriet McBryde Johnson’s account of her debate with Peter Singer over her own personhood to original pieces by authors like Keah Brown and Haben Girma; from blog posts, manifestos, and eulogies to Congressional testimonies, and beyond: this anthology gives a glimpse into the rich complexity of the disabled experience, highlighting the passions, talents, and everyday lives of this community. It invites readers to question their own understandings. It celebrates and documents disability culture in the now. It looks to the future and the past with hope and love.