Medical Illnesses

Leaving London to return home to rural South Wales, Robyn finds that it's her old life - same teddy bears resting on her pillow, their bodies tucked under the duvet; same view of the garages behind which she'd had her first cigarette and first kiss - but so much has changed. Her dad, the proud, charmingly intelligent self-made man who made people laugh, was in the grip of early onset Alzheimer's. His brilliant mind, which saw him building power stations and literally bringing light into the lives of others, had succumbed to darkness.

In November of 1970, the Finell family's lives were changed forever by a family vacation to Acapulco. Seven-year-old Stephanie fell ill soon after their return to the United States, but her mother, Karin, thinking it was an intestinal disorder, kept her home from school for a few days. She was completely unprepared when Stephanie went into violent convulsions on a Friday morning. Following a series of tests at the hospital, doctors concluded she had contracted viral equine encephalitis while in Mexico.

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.

⭑⭑⭑⭑⭑ This was a perfect story for now, due to the virus pandemic. I could really relate to the story and some of the issues that the isolation has caused. - Amazon Reviewer ⭑⭑⭑⭑⭑ Al Macy voiced many of the fears I'm experiencing, strictly sheltering from COVID-19. It helps to see them in writing & know that I am not alone! - Amazon Reviewer Attorney Garrett Goodlove has a strong bond with his twin sister, Carly. They’re soul mates. Doesn’t mean they always get along. Over the years, Garrett has found that the only way to tolerate his reckless and headstrong sibling ...

Pro football Hall of Famer Jim Kelly and his wife, Jill, were catapulted from a seemingly fairy-tale life of celebrity into a world of private struggle and medical uncertainty. What the public didn’t know, however, was that behind the scenes lurked more than a family’s pain at the dire prognosis of their only son. Hunter’s illness exposed the troubled depths of a marriage that had long been shadowed by uncertainties of its own.

Almost 11,700 people are diagnosed each year with a primary brain tumor, including 500 children and young people – that's 32 people every day. There are more than 120 different types. This book is one family's touching account of living with a brain tumor spanning over a decade.

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.

Life Blood, written by a renowned leukaemia physician, tells unforgettable stories of his leukaemia patients’ battles to be cured but also uniquely describes the stresses that doctors face when looking after extremely ill young people during an extraordinary time in their lives. In reflecting on his long and illustrious career, Professor Marks’ memoir offers frank descriptions of his own medical family, some personal experiences of ill-health and his relationships with colleagues and patients in the NHS. Partly written during the Covid pandemic and as he approached retirement, Life Blood offers highly informed and compassionate views on modern medicine, from a pivotal point in both the author’s own professional life and the history of healthcare.

Thriving with cancer. Survival doesn’t have to be a cancer patient’s only goal, and feeling overwhelmed doesn’t have to describe what it’s like to go through treatment. Focusing on one’s purpose and goals can make every day more manageable. Conscientious planning can help to lower anxiety, boost overall well-being, and even make room for moments that are full of life’s exuberance. This audiobook tackles personal and family issues that aren’t often raised by medical professionals and shines a light on what matters most: experiences that give life meaning and purpose.

Gulf war syndrome: fact or fiction? Saudi Arabia, 1991. Troops are in a state of high alert. The chemical warfare detectors have sounded, and the soldiers scramble into their protective suits. In terse silence, they remind themselves of the vaccinations that will protect them. Then the all clear sounds, and the troops rejoice that they are unharmed. Or so they think.

After suddenly being diagnosed with a rare form of aggressive cancer, I immediately started spiraling downward. Denial, loneliness, fear, depression, anger, and self-destructive behaviors. My life was a disaster. I was a mess. I was doing just about everything I was instructed not to. All sense of responsibility flew out the window, right along with my sense of morals. Further and further I slid into the deepest, darkest part of my life. I had come to terms with the fact that my life was over. I was going to die. Until I was rescued from not only cancer - but from myself.

When I graduated from medical school, a third of heart attack victims died at home or in the hospital. Heart rhythm disorders were killing or crippling hundreds of thousands of Americans every year. Severe heart failure was a death sentence. Preventive cardiology was practically unknown: the significance of high cholesterol was being debated, 50 percent of adults were smoking cigarettes, and high blood pressure was usually undetected and often poorly controlled. All of this changed for the better - much better - during the 47 years I practiced medicine and cardiology.

When you or someone you love is diagnosed with cancer it feels like your whole world is falling apart. Not knowing what will happen next is terrifying, and that is the main reason I wrote this book, hoping that my experience could help others. The first title of this book was, “My body is weak but my mind is strong”, starting out as a story about my personal battle with cancer, and that was the mantra I used to hype myself up before my final chemotherapy session.

In Making Tough Decisions About End-of-Life Care in Dementia, Dr. Anne Kenny, a skilled palliative care physician, describes how to navigate the difficult journey of late-stage dementia with sensitivity, compassion, and common sense. Combining her personal experience caring for a mother with dementia with her medical expertise in both dementia and end-of-life care, Dr. Kenny helps the listener prepare for a family member's death while managing their own emotional health.

Breasts: An Owner’s Manual is a straight-talking, myth and misconception-busting, strategy-filled guide to breast health. Sharing the latest on lifestyle choices that impact your risk factor including food, supplements, hormones and exercise, Dr. Funk demonstrates that you are so much more in control of whether or not you get breast cancer than you could ever dare to think. In fact, unless you carry a genetic mutation associated with breast cancer, the choices you make in your-day-to-day life trump genetics and family history when it comes to breast cancer risk, every time.

Diagnosed with a late-stage cancer after years of bungled and inadequate medical attention...and then to discover the best-practice chemotherapy is not available in your province. A true story, The Cancer Olympics is a suspenseful and poignant treatment of an unthinkable situation, an account of advocacy and survival that explores our deepest values regarding democracy, medicine, and friendship.

Called a "groundbreaking masterpiece" by Dr. Gregory O'Shanick, medical director emeritus of the Brain Injury Association of America, this is the gold edition of the unabridged audiobook of the critically acclaimed memoir The Day My Brain Exploded, which tells the story of Ashok Rajamani, a first-generation Indian American who had to relearn everything about life after a full-throttle brain hemorrhage at 25. With humor and insight, he describes the events of that day (his brain exploded just before his brother's wedding!) as well as the long, difficult recovery period. In the process he introduces listeners to his family - his principal support group as well as a constant source of frustration and amazement. Irreverent, coruscating, angry, at times shocking, but always revelatory, his memoir takes the listener into unfamiliar territory, much like the experience Alice had when she fell down the rabbit hole. That he lived to tell the story is miraculous; that he tells it with such aplomb is simply remarkable.

Renowned as a BBC journalist, Victoria Derbyshire has spent 20 years finding the human story behind the headlines. In 2015 she was diagnosed with breast cancer. With honesty and openness, she decided to live out her treatment and recovery in the spotlight in a series of video diaries. Victoria has kept a diary since she was nine years old, and in Dear Cancer, Love Victoria she shares her day-to-day experiences of life following diagnosis and coming to terms with a future that wasn't planned.

Passados dois anos da publicação de seu primeiro livro, Enquanto eu respirar, a jornalista Ana Michelle Soares segue inteira na vida. Em 2011, aos 28 anos, ela foi diagnosticada com um câncer de mama. Aos 32, a doença voltou e atingiu outros órgãos, sem possibilidade de cura. Agora, entre tratamentos e remissões, ela busca o que realmente importa: o sentido de estar aqui. Nesta obra AnaMi se rende à liberdade de descobrir que um diagnóstico não se resume ao que dita a biologia. Com mais paixão do que nunca, ela fala apenas de vida.

Lopsided is not your ordinary cancer memoir. Meredith Norton displays the razor-sharp wit of a master humorist as she chronicles her experience, from the first appearance of her bizarre symptoms to moving in with her compulsive parents and their five television sets.