Showing results by publisher "Audible Studios" in Physical Illness & Disease

The Future of Assisted Suicide and Euthanasia provides the most thorough overview of the ethical and legal issues raised by assisted suicide and euthanasia - as well as the most comprehensive argument against their legalization - ever published. In clear terms accessible to the general listener, Neil Gorsuch thoroughly assesses the strengths and weaknesses of leading contemporary ethical arguments for assisted suicide and euthanasia.

Somos lo que comemos, y por ello como padres hemos de educar a nuestros hijos en todo lo concerniente a la correcta alimentación. Se trata de una responsabilidad que no debemos eludir si queremos que los niños crezcan sanos.

A funny and poignant memoir that delves into the magic, fails, and meaning of fatherhood. Humorist and family man Jason Good is an only child with an atypical story to tell. His isn't the usual rant about how hard it is to be a modern father or a tale about a damaging relationship with his father. Jason grew up with a charismatic, communicative, affectionate, and frustrated political science professor for a father - a man who taught him most everything about how to be a dad, how to live.

The inside story of the most audacious public health campaign of the 21st century. In 2002, a dynamic doctor named Thomas Frieden became health commissioner of New York City. With support from the new mayor, billionaire Michael Bloomberg, Frieden and his health department team prohibited smoking in bars, outlawed trans fats in restaurants, and attempted to cap the size of sodas, among other groundbreaking actions.

Hilarious and heartbreaking, profane and profound, It Takes a Worried Man is the true story of a young husband and father whose life is changed forever by his wife’s breast cancer diagnosis. Following Brendan Halpin’s cranky, irreverent, and lustful thoughts through the diagnosis and treatment of his wife, Kirsten, It Takes a Worried Man is an unflinching and raw look at how cancer transforms a family. It’s also the funniest book about cancer you’ll ever read.

How will sex be after breast cancer? How does a couple cope with the sensitivities? For both women and men, the question is rarely asked. Soon after her 25th birthday, Katherine Schmidhofer was diagnosed with breast cancer, and her doctor advised an immediate mastectomy. Her breasts were removed, and she underwent ghastly sessions of chemotherapy and hormone therapy. She wondered whether she would ever have children. She mourned her incapacity to breastfeed.

Writer and political activist Mike Marqusee was diagnosed with multiple myeloma, a type of blood cancer, in the summer of 2007. At first, disinclined to share his misery with others, he was reluctant to write about his illness. But he then came to realize that doing so provided a precious continuity with his life as a writer before contracting the disease, and a way of reaching out to a wider world that the illness made physically less accessible.

At the peak of her career, classical homeopath and health-care columnist Katina Makris was stricken with a mysterious "flu". Only after five years of torment - two completely bedridden - and devastating blows to her professional and family life was Katina's illness finally diagnosed as Lyme disease.

After a routine pap smear in 2009, Angela Schmidt Fishbaugh discovered that she had tested positive for BRCA1, a genetic trait that predisposed her to breast and ovarian cancer. After her initial shock - and subsequent to consulting with medical professionals, friends, and family - the proactive mother and teacher embarked on a mission to nip the issue in the bud.

Published in partnership with the International Association for the Study of Pain, A Nation in Pain offers a sweeping, deeply researched account of the chronic pain crisis, from neurobiology to public policy, and presents practical solutions that are within our grasp today. Drawing on both her personal experience with chronic pain and her background as an award-winning health journalist, she guides us through recent scientific discoveries, including genetic susceptibility to pain.

The Headache Godfather traces the life of Seymour Diamond, MD, who was born in 1925, the son of Jewish immigrants from Ukraine and Slovakia, in Chicago, Illinois. Dr. Diamond revolutionized the practice of headache as a medical specialty when he opened the United States' first private headache practice, the Diamond Headache Clinic, in 1974. It quickly became a headache haven for sufferers from around the world.

Unbreakable Bonds tells 10 touching stories of mothers who spent years aiding the recovery of their children, US soldiers and Marines who suffered severe injuries during the War on Terror. The survival of these wounded warriors is a testament not only to the extraordinary efforts of military medical personnel and their own inner fortitude, but also to their mothers.

Autism shakes up your world. It has changed my life and I wasn't even the one diagnosed with it. My brother's name is Ethan Wolfgang, but we call him Deets. He is one of the greatest gifts my family has ever received. And one of the most challenging.

Written by a leading dermatologist, The Blue Man and Other Stories of the Skin provides a compelling and accessible introduction to the life of our largest organ, while also recounting the author’s experiences with memorable patients he has treated who suffer from mysterious skin conditions. Robert Norman begins by highlighting the qualities of the skin, tracing the history of its conditions and diseases, then examining the cultural, social and psychological impact of both color and irregularity.

Ultimately, Hadler's insights illustrate how the state of the science can and should inform the art and practice of medicine as well as public policy. Stabbed in the Back will arm any reader with the insights necessary to make informed decisions when confronting the next episode of low back pain.

Two families came together in the waiting room of a Denver hospital on May 11, 2004, to await kidney transplants for loved ones. In the first operation, Gregg Farber, 32, a real estate executive, donated a kidney to his father, Steve, a 60-year-old Denver lawyer and power broker. In the second, Guatemalan refugee and landscaper Ernesto Delaroca, also 32, donated a kidney to his sister Sandra, 19, a restaurant worker.

Hundreds of thousands of people die every year from malaria. No one's quite sure of the exact number. It's just too difficult to keep track of the disease as it tears through more than 200 million cases each year, many of them in countries wracked by war and blighted by other problems. In The Deadly Air, Christian Jennings mixes together his own experiences of suffering from malaria with a history of mankind's struggle with the disease.

Dr. Mackowiak, a professor at the University of Maryland School of Medicine, offers a gripping and authoritative account of 13 patients who took center stage in world history. The result is a new understanding of how the past unfolded, as well as a sweeping survey of the history of medicine. What was the ailment that drove Caligula mad? Why did Stonewall Jackson die after having an arm amputated, when so many other Civil War soldiers survived such operations?

The word conquer has changed meaning for Bryan Anderson. As a U.S. army sergeant in Iraq, it meant taking down the enemy. After becoming Iraq’s fourth triple amputee from a roadside explosive, what he had to conquer got a bit more personal. On October 23, 2005, the moment Bryan looked down and realized he no longer had legs, he cracked a joke. It was a tragedy that could break many, but Bryan transformed it into something positive, something that propelled him forward.

Ticked: The Battle Over Lyme Disease in the South is the second installment of Discover In-Depth, Discover magazine's new longform series. In this deep investigation of the science surrounding Lyme disease, writer Wendy Orent dissects how tick-borne illness is diagnosed in the Southern United States, where the Centers for Disease Control and Prevention (CDC) do not recognize Lyme even though thousands of people in the South have reported Lyme-like symptoms and debilitating illness.