Medical Diseases

"The best we can hope for you to live is 20 to 24 months...." That was the report given to Durell and Susan Tuberville by the physician who diagnosed Durell with stage four colorectal cancer. Durell and Susan were now faced with the question of how to live their final months together. How do you respond when faced with adversity in your own life? In this inspirational autobiography, you will hear about Durell's and Susan's decision to "live the miracle" rather than prepare for death. You will learn of the miracles of life that have given them success in their cancer journey.

Bauchweh oder Durchfall hat jeder mal. Aber was, wenn sie zum ständigen Begleiter werden und ein normaler Alltag kaum möglich ist, weil der Darm nicht mitspielt? Hunderttausende leiden allein in Deutschland an Colitis ulcerosa, einer chronischen Entzündung des Dickdarms. Einer von ihnen: TV-Star und Influencer Philipp Stehler. Nach Jahren des Verdrängens, des heimlichen Leidens und der ständigen Medikamenteneinnahme entschied sich der Frauenschwarm, mit dem Tabu zu brechen und offen über seine Krankheit zu sprechen.

Off Our Chests recounts the story of Liza and John’s experience with her diagnosis and treatment. Written in alternating voices, Liza details her treatment and the complex decisions she had to make throughout her course of chemotherapy and radiation, including clinical trial participation and an elective double mastectomy, with the added complexity of being treated at the cancer center of which John was the chief of hematology and oncology and dealing with the emotional impact of knowing she may die as a young woman with young children.

The Long Tale of Tears and Smiles explores an immigrant oncologist’s journey of triumphs and struggles, from growing up in Syria, to the tragic death of her brother, to her experiences as a young immigrant medical student and trainee in the USA. Walk through her anguish witnessing the civil war in Syria and its devastation; see her become a practitioner, watching the field of oncology evolves throughout the years.

Forfatter og antropolog Ina Kjøgx Pedersen har været på feltarbejde i sin egen familie. Hendes idé var på nærmeste hold at følge sin mors demenssygdom; den sygdom, som er udråbt til at være en af vor tids største personlige og verdensøkonomiske katastrofer, som i ringe omfang lader sig behandle, og som i sundhedsvæsnet kun kan måles negativt: I form af rask tilbagegang. Men ville det også opleves sådan for hende i virkeligheden?

This isn't just a real-life story of a second chance at love - it is a story about a loving husband who would sacrifice everything to ensure his wife’s beautiful smile never wavers. Shana and Schirra’s story will take you on a journey into the joys in marriage, the pains cancer patients face, and the beauty in true love. They are proof that real love exists and it doesn’t need physical well-being to thrive. Through their faith in God and devotion to one another, an eternal love arises that cannot be replaced or shattered.

Nicky, a witty, intelligent, and clever 13-year-old, was diagnosed with a rare childhood bone cancer. However, this book is about more than cancer and its treatment and the fight to survive. It's about more than a mother and her son who accepted his mortality at such a young age and the strength and love between two loving souls.

So, you were just diagnosed with breast cancer - what now? Hold on! There is hope. You can take control of your journey to recovery, feel connected to yourself and others, and get through this. Join Birgitte (Deda) Wilms as she recounts her breast cancer journey and learn how she got through all of her therapy, treatments, surgeries, and turned her experience into a blessing. Birgitte's road wasn't easy, but she is now fully cured and thriving, and you can be as well. Don’t go through this journey alone; listen to Live Well beyond Breast Cancer today.

This book is written from an actual survivor who wants to provide helpful information to anyone who is going through their own serious health issue or is close to someone who is battling through a major medical problem. The author was a caregiver and then, went through his own cancer diagnosis and treatments. These provided the experiences to learn how to recognize and manage the physical, mental, emotional, and spiritual challenges that everyone must face during these difficult times.

If you’ve ever been ugly dumped, knocked off your feet, financially devastated, stunned by a potentially fatal diagnosis, or paralyzed by fear, you’ll find comfort and strategies for surviving and eventually thriving in this book. Her surprising journey through the maze of illness, treatment, surgery, and recovery, along with her stubborn daily practice of gratitude, even when she wanted to throw her gratitude journal off a cliff, will leave you laughing, crying, and hopefully feeling grateful, even when it seems impossible.

Being diagnosed with cancer is frightening; learning that the cancer is late stage takes that fear to unknown depths. After a year of brutal treatment, Mo Haque heard the dreaded words, 'There is nothing else we can do for you.' His cancer was terminal and left him questioning the price we put on life. Three years on from the 'small chance' of survival the experts had given him, Mo shares his incredible story: of despair and suffering, of hope and healing, of vulnerability and authenticity. This audiobook is for anyone going through the most challenging of times.

Maneater is a personal account by a specialist who approaches her work like a forensic scientist or a case-hardened private eye. Dr. Pamela Nagami is a leading authority on infectious diseases and her stories will shock, amaze, and warn listeners.The patients in Maneater are ordinary Americans. When Danielle Jordan innocently ordered a salad for lunch in Puerta Vallarta she had no idea she had just become the "host" to an organism that six years later would grow into a worm and burrow into her brain.

Dr. George Cotzias lived a large life. He stood over six feet tall; he drank Metaxa like milk; he smoked cigarettes as if eating candy. He bullied patients, sometimes looming over their wasted bodies. He had “a stare as strong as death”. His passion for women, his wife, and others was infamous. His voice boomed through the halls of the hospital where he was chief of physiology research.

Every 69 seconds, someone is diagnosed with Alzheimer's disease. Of the top 10 killers, it is the only disease for which there is no cure or treatment. For most people, there is nothing that they can do to fight back. But one family is doing all they can. The DeMoe family has the most devastating form of the disease that there is: early onset Alzheimer's, an inherited genetic mutation that causes the disease in 100 percent of cases, and has a 50 percent chance of being passed onto the next generation.

Five months pregnant, Amanda Adams and her husband were given two abysmal choices regarding her pregnancy: force her baby to fight for his life through countless invasive and dangerous surgeries, or perform a late term abortion. Despite the fact that Liam was missing half his heart, Amanda chose life. Amanda's emotional plate was full as she found herself redefining the usual expectations a mother has for her child. Instead of wondering where he'd go to college, she wondered if he would survive his first birthday. The eventual acceptance of Amanda's grief helped her accept her new role as a powerful advocate.

Throughout history, there have been numerous epidemics that have threatened mankind with destruction. Diseases have the ability to highlight our shared concerns across the ages, affecting every social divide from national boundaries, economic categories, racial divisions, and beyond. Whether looking at smallpox, HIV, Ebola, or COVID-19 outbreaks, we see the same conversations arising as society struggles with the all-encompassing question: What do we do now?

The Cancer Problem offers the first medical, cultural, and social history of cancer in 19th-century Britain. It argues that it was in the 19th century that cancer acquired the unique emotional, symbolic, and politicized status it maintains today. Through an interrogation of the construction, deployment, and emotional consequences of the disease's incurability, this book reframes our conceptualization of the relationship between medicine and modern life and reshapes our understanding of chronic and incurable maladies, both past and present.

What's one of the leading causes of premature death in the Western world? Loneliness. And whom does loneliness kill? Who does it not? For every citizen in every one of the world's technologically advanced nations--from homemakers to businesspeople, from college students to school dropouts, from the elderly to the young--loneliness is an unrecognized, unguarded-against stalker.

A journey through the deepest valleys and highest peaks of parenting. When a two-month old baby falls ill, his apparently ordinary symptoms turn out to signal a rare and lethal immune deficiency. For parents Miguel Sancho and Felicia Morton, the discovery that their son, Sebastian, has chronic granulomatous disease (CGD) upends their lives and leaves the family with few options, all of them terrifying.

In this book, Stephen G. Post offers new perspectives on the worth and dignity of people with Alzheimer's and related disorders despite the negative influence of "hypercognitive" values that place an ethically unacceptable emphasis on human dignity as based on linear rationality and strength of memory. With vignettes and narratives, he argues for a deeper dignity grounded in consciousness, emotional presence, creativity, interdependence, music, and a self that is not "gone" but "differently abled."