Medical Diseases

Straight out of today's hospitals and labs, and tomorrow's headlines, comes a frightening, scalpel-sharp thriller from medical insider Joshua Spanogle. In an astounding debut, Spanogle takes us on an all-too-real race against time as a young doctor enters the dark side of scientific research, desperate to stop a terrifying epidemic before it is too late.

These heartwarming and inspiring stories by brave women and men who have survived breast cancer are a must-listen for anyone personally or indirectly afflicted by the disease. How We Beat Breast Cancer brings together the experiences, thoughts, struggles, and victories of unique women and men from all walks of life, who tell the stories of their battles with breast cancer. Their narratives portray both the good and the bad in a real, candid language, sharing everything from diagnosis, through treatment, to life with and after cancer.

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.

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.

Following the trail of an unexpected family connection, acclaimed journalist Pam Fessler has unearthed the lost world of the patients, nurses, doctors, and researchers at Carville who struggled for over a century to eradicate Hansen's disease, the modern name for leprosy. Amid widespread public anxiety about foreign contamination and contagion, patients were deprived of basic rights - denied the right to vote, restricted from leaving Carville, and often forbidden from contact with their own parents or children.

If you have Lyme disease, you know firsthand the desperation that comes from being misdiagnosed, misunderstood, and misdirected. You need straight answers and real solutions, but all you get is the runaround. Riding high as a hard-driving entrepreneur in the solar industry, Taylor Nelson contracted Lyme disease in his mid-twenties. Spiraling down swiftly, he tried everything to feel like himself again, turning himself into a human guinea pig. Taylor shares his deeply personal story, what he tried, how it worked, and how to live a full life in the face of a devastating disease.

Bettina Greschner hat sich lange Zeit ihres Leben nicht erwünscht und nie gut genug gefühlt. Das Leben ging nicht gerade zimperlich mit ihr um. Aufgewachsen mit einem alkoholabhängigen Elternteil, der tödliche Verlust des Lebenspartners kurz vor der geplanten Hochzeit, 2011 die Diagnose "Brustkrebs" und zeitgleich die Selbständigkeit mit einem Möbelgeschäft, welche damals unter keinem guten Stern stand. Was nun? Warten bis es noch schlimmer wird und noch weiter bergab geht? Nein! Das war keine Option.

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.

Hayley Okines is like no other 13-year-old schoolgirl. In Old Before My Time, Hayley and her mum, Kerry, reflect on her unusual life. Share Hayley’s excitement as she travels the world meeting her pop heroes Kylie, Girls Aloud, and Justin Bieber and her sadness as she loses her best friend to the disease at the age of 11. Now as she passes the age of 13 - the average life expectancy for a child with progeria - Hayley talks frankly about her hopes for the future and her pioneering drug trials in America which could unlock the secrets of ageing for everyone....

Dinah Roseberry, author and editor for the prominent company Schiffer Publishing in Pennsylvania, is a strange one. Fighting stage four breast cancer since 2012 and still in remission, she's taken the strange in her life to manage and thrive during a most horrendous journey. Using her paranormal and mind/body/training, she has found some techniques to make things a bit smoother along the way, and now she steps up to the plate to share those methods with you.

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.

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.

"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.

L'histoire célèbre les victoires que les médecins ont remportées sur les maladies. Mais elle néglige leurs patients dont les troubles, les souffrances ou les plaintes ont inauguré de nouveaux diagnostics, remis en cause certaines théories médicales ou ouvert des perspectives thérapeutiques inédites.

Mysterious and misunderstood, distorted by biblical imagery of disfigurement and uncleanness, Hansen's disease or leprosy has all but disappeared from America's consciousness. In Carville, Louisiana, the closed doors of the nation's last center for the treatment of leprosy open to reveal stories of sadness, separation, and even strength in the face of what was once a life-wrenching diagnosis. Drawn from interviews with living patients and extensive research in the leprosarium's archives, Carville: Remembering Leprosy in America tells the stories of former patients.

In 1918, a world war raged, and a lethal strain of influenza circled the globe. In the midst of all this death, a bizarre disease appeared in Europe. Eventually known as encephalitis lethargica, or sleeping sickness, it spread worldwide, leaving millions dead or locked in institutions. Then, in 1927, it disappeared as suddenly as it had arrived. Asleep, set in 1920s and '30s New York, follows a group of neurologists through hospitals and asylums as they try to solve this epidemic and treat its victims - who learned the worst fate was not dying of it, but surviving it.

Fourteenth-century physician Alejandro Guzman, caught performing an autopsy in Spain, flees across Europe at the time of the Black Death to escape execution for his heretical deed. When he arrives in the Papal city of Avignon, he is conscripted against his will to serve as a Plague Doctor in the court of England's Edward III. Unfolding in a dramatic counterpoint is the story of American medical archaeologist Janie Crowe, in England at the turn of the 21st century to recover from the tragic loss of her family.

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?