Medical Diseases

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.

From a darkened world, bound by four walls, a young woman called Jessica tells the tale of her battle against the M. E. Monster. The severest form of a neuroimmune disease called Myalgic Encephalomyelitis went to war with her at just 15 years old. From beneath her dark glasses, Jessica glimpses a world far different from the one she remembers as a teenage schoolgirl. This true story follows her path as she ends up living in a hospital for years with tubes keeping her alive.

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.

After a hard-fought battle in the heart, Progen has defeated the agents of the entity that wants to destroy the body he is determined to control. It was a temporary defeat, however, as the entity retreated up into the body’s brain, safely entrenched behind the blood-brain barrier that is preventing the dungeon crystal from accessing the coveted home base of the central nervous system. As he further establishes his control over the different systems that he can access, a grievous wound to the body creates a problem that could spell the end of his objective.

This book covers the history of 12 important diseases and addresses public health responses and societal upheavals.

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.

Thyroid management in the United States has not significantly changed over the past 40 years despite reams of new research that is mostly ignored or even vilified by the medical establishment. There has become a substantial difference between what is considered the standard of care of thyroid management and what the latest research and evidence shows is most beneficial. As a result, thyroid patients are feeling worse and getting less benefit than ever before despite using the standard thyroid treatment protocols.

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?

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.

What is it like to encounter cancer? How does it feel to face the unknown, to enter a world of hope, loss, and dread? From the diagnosis of his childhood friend’s mother to his poignant memories in the lab, David Scadden’s seen the unknown world of cancer from the lens of a young boy, a classmate, a researcher, a friend, a doctor, and a neighbor. Scadden chronicles his personal memories of cancer - his visits to his sick neighbor and his classmate who left school and never came back.

A coming-of-age memoir for modern times, Bleeder is the incredibly compelling tale of author Shelby Smoak. A hemophiliac, Smoak discovered he had been infected with HIV during a blood transfusion at the start of his college career. This devastating and destabilizing news led Smoak to see his world from an entirely new perspective, one in which life-threatening illness was perpetually just around the corner. Set in the 1990s along the North Carolina coast, Bleeder traces Smoak’s quest for love in a world that feels increasingly dangerous.

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.

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 Smooth River is the remarkable story of how a well-known public relations expert and her husband met her stage 4 pancreatic cancer head-on. With vigor and strength, they deployed all they and medicine had to offer. But in contrast to narrow conventional approaches, the couple developed a far more expansive view of what strength means in response to a crisis for which there are no medical cures. They called this the Smooth River.

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.

In January of 2021, I was given an “all clear” on my cancer. Nine months later my “all clear” turned into “two to four months to live”. To say that was a shock to me would be a gross understatement. The only way I could handle it mentally was to compartmentalize it in my mind and write about it.

"Du har cancer Charlotta" sa läkaren. 35 år gammal fick jag aggressiv trippelnegativ bröstcancer. Mina barn var då ett, två och fyra år. Jag stekte pannkakor och planerade inför min begravning. När Charlotta får reda på att hon är gravid med sitt fjärde barn är hon redan i artonde veckan. Det är bara sju månader efter hennes senaste cellgiftsbehandling och läkarna hade sagt att hon inte skulle kunna få fler barn. Hon överväldigas av känslor. Lycka. Rädsla. Hon börjar skriva ner sina tankar, för att komma underfund med tankarna om allt det ljusa och allt det mörka.