Ergebnis für "Whit" in Medizin

Ryan White was a typical 13-year-old living in a small town in the Midwest. Then, it was discovered that Ryan had contracted AIDS through tainted blood products he had been given for his hemophilia. Denied the right to return to school, he went to court.

Another “pitch-perfect book of short essays” (New York Times Book Review) from the acclaimed author of Blood of Strangers, this one exploring the contemporary practice of medicine from the perspective of a doctor with 25 years of experience in the ER. In the late 1990s, a young physician in...

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.

When Damon Tweedy begins medical school, he envisions a bright future where his segregated, working-class background will become largely irrelevant. Instead, he finds that he has joined a new world where race is front and center. The recipient of a scholarship designed to increase black student enrollment, Tweedy soon meets a professor who bluntly questions whether he belongs in medical school, a moment that crystallizes the challenges he will face throughout his career.

In the 1980s, as HIV/AIDS ravaged queer communities and communities of color in the United States and beyond, a straight white teenager named Ryan White emerged as the face of the epidemic. Diagnosed with hemophilia at birth, Ryan contracted HIV through contaminated blood products.

Although we rely on physicians, calling on them at birth and death and every medical event in between, rarely do we consider the personal challenges faced by doctors-to-be. In 2005 author Jacqueline Marino and photojournalist Tim Harrison had the unprecedented opportunity to chronicle the experience of three students as they learned to become doctors at the Case Western Reserve University School of Medicine.

This must-listen account of starting at the lowest rung on the production ladder among enormously famous and outrageously demanding people will be devoured for its insights, gossip, humor, and storytelling. Married and with a child, the author takes unpaid gigs to get a foot in the door and eventually ends up working on all seasons of The Sopranos, often named the best TV show ever.

In the tradition of Robin Cook, Michael Crighton, and Samuel Shem, The Long White Coat is a story of medicine’s power, arrogance, and fallibility, based on real and painful clinical experience, told with humor and compassion. One editor, James O’Shea Wade, said, “The Long White Coat may convince the appalled and enthralled listener to never, ever go near a hospital again unless, like all the patients and doctors in this compelling narrative, they have no choice.

Without self-pity, former New York City newspaperman and prize-winning magazine editor, Robert C. Samuels tells his own harrowing story of medical survival. He's filled it with tears, humor, love, and triumph.

InHumana: An American Healthcare Story tells how an only child was conscripted into a war with a soulless monstrosity that repeatedly tried to throw his widowed mom's life away with the surreptitious aid of unregulated artificial intelligence.

Despite the fact that African American lineage has given rise to such undeniable talent, intelligence, and genius as that of Dr. Charles Drew, Dr. Daniel Hale Williams, Dr. Rebecca Lee Crumpler, and an exhaustive list of many, many others, the proverbial badge of honor in "the white coat" seems to exist as only a mirage of truth until it is achieved. For every budding and current Black doctor seeking guidance, if ever you've wanted to know what it takes to get in, how to stay in, and what it takes to win, consider this the blueprint.

I once heard someone say, "You cannot aspire to be something you have never seen." This book is not only for every little Black girl out there who has dreamt of wearing a white coat and stethoscope but also for all the little Black girls who have not dreamt of it because they have never thought it possible.

“I had the moment. The Moment. When life was as I expected, until it wasn’t.” That was the day in 2004 that Lauree Ostrofsky came face-to-face with the little white blob, an acoustic neuroma brain tumor. A series of scary moments and missteps follows and ultimately lead her to launching #hugtour, plotting routes to office buildings and coffee shops hugging people she cares about along the way. The process teaches her that running hugs in traffic are exhilarating and that unabashedly sharing love is more worthwhile than she could ever have imagined.

You can't make this stuff up. A collection of short, true stories that have made me who I am. Some are funny, some serious, some sad, some empowering. Beginning with some experiences as a child, these stories venture though home health care, a haunted nursing home, and the ER.

More of: You can't make this stuff up. A collection of true, short stories from the experiences that made me who I am. Some are funny, some serious, some sad, some empowering. Starting with some stories from my youth, then a bunch of stories of mostly medical related happenings.

Richard Carlson Jr. was diagnosed with paranoid schizophrenia when he was 21 years of age. His illness first manifested when he was an early adolescent. Modern psychiatry greatly failed Richard for over a decade. Then, after an incident involving the police, he truly understood that his diagnosis was real, and finally began the long process of recovery. Over 10 years later, his life is greatly improved. In the course of his treatment, Richard also recovered from depression, obsessive-compulsive disorder, and lethargy.

In this highly personal account, Dr Gibbs documents the effect his diagnosis has had on his life and explains his advocacy for improving early recognition of Alzheimer’s. Weaving clinical knowledge from decades caring for dementia patients with his personal experience of the disease, this is an optimistic tale of one man’s journey with early-stage Alzheimer’s disease.

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.