Medical Biography

In this award-winning memoir, two sisters reckon with the convalescence and death of their outlandishly tyrannical mother and the care of their psychologically terrorized father, all relayed with dark humor and brutal honesty.

Christine Bryden was a top civil servant and single mother of three children when she was diagnosed with dementia at the age of 46. Since then she has gone on to challenge almost every stereotype of people with dementia. This is a vivid account of the author's experiences of living with dementia, exploring the effects of memory problems, loss of independence, difficulties in communication and the exhaustion of coping with simple tasks. She describes how, with the support of her husband, Paul, she continues to lead an active life and explains how professionals and carers can help.

When Shannon Sovndal started medical school, he was confident and motivated and felt invincible. He thought he was going in with his eyes wide open. Really, he had no clue. Nothing could prepare him for the harsh reality of being a compassionate human and working as an ER doctor. In his emotionally charged memoir, Sovndal examines the tenuous balance between trying to compartmentalize the trauma of tragedy while also preserving his own humanity.

ALS is a deadly disease that didn't want to let go of me. I went from hope to planning my own death as a way of escaping this demon. My journey is a view into the life of a person who needs 24-hour care, never any privacy. I was given 18 months to get my affairs in order. That lead me to seeking a higher power than the doctors. I have never witnessed an energy healing until it happened to me. This book is my call to each of you and your family who are challenged by ALS. My frame of mind was my only power.

In 2017, David got what he thought was a mild touch of the flu. This book is the story of why David would make a lousy doctor. Contrary to the book’s title, David had lymphoma and it was terminal. But A Mild Touch of the Cancer isn’t your standard "how I survived" compendium. It is a hilarious tale, written while battling one of life’s greatest challenges. It’s a book about living with optimism and positivity, by a self-proclaimed Genetically Modified Organism.

Free Refills is the harrowing tale of a Harvard-trained medical doctor run horribly amok through his addiction to prescription medication, and his recovery. Dr. Peter Grinspoon seemed to be a total success: A Harvard-educated MD with a thriving practice; married with two great kids and a gorgeous wife; a pillar of his community. But lurking beneath the thin veneer of having it all was an addict fueled on a daily boatload of prescription meds. When the police finally came calling - after a tip from a sharp-eyed pharmacist - Grinspoon's house of cards came tumbling down fast.

Deeply touching and uplifting, What You See When You Can't See offers a way of looking at the world through different eyes and a road map to finding bliss in the simplest of things. Zena was born with Marfan Syndrome, a connective tissue disorder leaving her nearly completely blind, yet she kept this condition hidden from the world for four decades - until she met Munch. A guide dog with a huge personality, Munch made Zena's invisible disability suddenly plain for all the world to see. This book shares the story of Zena's journey with Munch....

Where does one go without health insurance, when turned away by hospitals, clinics, and doctors? In The People’s Hospital, physician Ricardo Nuila’s stunning debut, we follow the lives of five uninsured Houstonians as their struggle for survival leads them to a hospital where insurance comes second to genuine care.

An easy to digest, honest and personal account of the life of a surgeon and the effect that it has on his wife and family. The listener is taken behind the scenes as fascinating patient stories are used to illustrate what the job entails and the pressures and emotions that result; the child with life-threatening injuries or the patient needing end of life care. Incidents of medical malpractice, sexism and other problems encountered within the NHS are also related, again exemplified by authentic clinical stories.

Sönke Nissen führte ein Leben wie aus dem Bilderbuch: Vorzeigesohn, Traumkarriere, Wunschfamilie. Dann fiel von einem Tag auf den nächsten das ganze Kartenhaus in sich zusammen. Dem schleichenden Zerfall seiner Ehe folgte die Kündigung als Geschäftsführer und schließlich binnen weniger Tage die Diagnose einer degenerativen, fortschreitenden Muskelerkrankung. Was sich liest wie eine zerstörte Biografie, wurde zum Beginn einer märchenhaften Wandlung.

Me lo dijo sin preámbulos, pero no me tomó por sorpresa.A principios de 2022, mi padre, Carlos Alberto Montaner, me encomendó la misión más difícil y dolorosa de mi vida: "Te pido que me ayudes a morir". Más de seis años después de ser diagnosticado en Estados Unidos con párkinson sus capacidades físicas habían mermado considerablemente y la enfermedad comenzaba a hacer mella en sus facultades cognitivas.

On July 4th, 2013, Connor Sparrowhawk, also known as Laughing Boy or LB, was found dead in a specialist NHS unit. Connor, who had autism and epilepsy, had a seizure while in the bath, and no member of staff was on hand to stop him from drowning. An entirely preventable death. Sara Ryan presents a frank, sometimes funny and touching account of her son's early life and preventable death and the unfolding #JusticeforLB campaign.

"Ein Taxi ist so teuer und ich zahle doch auch Krankenkassenbeiträge." Oder "Wenn Sie mich mitnehmen, komme ich ja schneller dran!" Solche Sätze hört Luis Teichmann oft. Er fährt seit sieben Jahren im Rettungsdienst und Bagatelleinsätze sind hier nicht die einzige Herausforderung: Nachtschichten, körperlich schwere Arbeit, gewalttätige Übergriffe und die psychische Belastung rücken seinen Job aus der Komfortzone. Da ist zum Beispiel der stadtbekannte Mann, der bis zu viermal am Tag die 112 wählt, an 365 Tagen im Jahr – und jedes einzige Mal muss ein RTW ausrücken.

Patti M. Hall’s life is pitched into an abyss of uncertainty when a golf ball-sized tumour is discovered in her teenage son’s head and he is diagnosed with gigantism, a disease of both legend and stigma. After scrambling to access a handful of medical experts in the field, Patti learns that her son could grow uncontrollably, his mobility could be permanently limited, and his life could be cut short without timely and aggressive treatment. Patti’s attention shifts fully to her son, away from her relationships as well as her own career and health.

When her husband, Alan, is injured in a speedboat accident, Cathy Crimmins reluctantly assumes the role of caregiver and learns to cope with the person he has become. No longer the man who loved obscure Japanese cinema and wry humor, Crimmins’ husband has emerged from the accident a childlike and unpredictable replica of his former self with a short attention span and a penchant for inane cartoons. Where Is the Mango Princess? is a breathtaking account that explores the very nature of personality - and the complexities of the heart.

Born in rural Mexico, Eduardo “Lalo” García Guzmán and his family left for the United States when he was a child, picking fruits and vegetables on the migrant route from Florida to Michigan. He worked in Atlanta restaurants as a teenager before being convicted of a robbery, incarcerated, and eventually deported. Lalo landed in Mexico City as a new generation of chefs was questioning the hierarchies that had historically privileged European cuisine in elite spaces. At his acclaimed restaurant, Máximo Bistrot, he began to craft food that narrated his memories and hopes.

These are the extraordinary realities of the NHS front line. From the historic junior doctor strikes to the 'humanitarian crisis' declared by the Red Cross, the overstretched health service is on the precipice. This is a powerful polemic on its systematic degradation and a letter of optimism to that same health service and those who support it. It captures with tenderness a new doctor's experiences of an NHS at breaking point.

In Dottoressa: An American Doctor in Rome, Levenstein writes, with love and exasperation, about navigating her career through the renowned Italian tangle of brilliance and ineptitude, sexism and tolerance, rigidity and chaos. Part memoir starting with her epic quest for an Italian medical license and part portrait of Italy from a unique point of view, Dottoressa is packed with vignettes that illuminate the national differences in character, lifestyle, health, and health care between her two countries.

For nearly three decades, Dr Colin Manock was in charge of South Australia's forensic pathology services. In cases of unexpected or unexplained death, it was his job to determine when a person took their final breath, and whether they had died naturally - or not. But Manock did not have the necessary training for such a specialist role, and made serious errors in several major cases. The full extent of his wrongdoing, and the exact number of cases impacted by it, remain a mystery more than twenty-five years after he retired.

While in her early-30s, Anna Byrne was diagnosed with a rare and aggressive form of lymphoma. Over the next seven years, she endured four relapses, two stem cell transplants, and spent over 2,000 hours in Canadian hospitals. In 2014, she was given two years to live. Despite the odds, Anna left treatment cancer-free. She became a hospice volunteer and met Eleanor, a woman in her 70s whose death was imminent, and the two formed an unlikely friendship. Part memoir, medical guide, and spiritual text, Seven Year Summer explores the nuances of healing and hope.