Titoli in Medico

I juli 2014 fick Sven Erik Nordin beskedet att han hade en aggressiv form av cancer i underlivet. Samtidigt fick han veta att hans enda chans att överleva var att genomgå en omfattande operation som bland annat innebär att hela penis skulle avlägsnas. Efter en kort betänketid bestämde sig Sven Erik för att inte följa läkarens råd och tackade nej till behandling. I stället började han febrilt leta efter alternativa metoder som kunde bota honom. I dag är han friskförklarad!

Varje år får omkring 1300 personer någon typ av hjärntumör, bara i Sverige. Man kan råka ut för en godartad (benign) eller elakartad (malign) tumör och symtomen är ungefär de samma för båda sorterna. 2011 fick mamman och projektledaren Åsa Tönne diagnosen 'malign hjärntumör.' Hela hennes liv rasade samman och en envis kamp mot klockan och sjukdomen startade.

PORUSZAJĄCA KSIĄŻKA O MIŁOŚCI I MEDYCYNIE. O DZIAŁANIU MÓZGU W EKSTREMALNEJ SYTUACJI. O HEROICZNEJ WALCE O RODZINĘ, GODNOŚĆ I NADZIEJĘ. W 2011 roku u męża dr Lisy Shulman, dr. Williama Weinera, zdiagnozowano raka. Zmarł siedemnaście miesięcy później. Oboje byli neurologami. NAGLE Z LEKARZY STALI SIĘ PACJENTAMI. Neurolog jest ekspertem w nauce o mózgu, jednak nikt nie jest dobrze przygotowany na kolejne etapy walki ze śmiertelną chorobą. Ta książka jest poruszającym zapisem przemyśleń obojga lekarzy.

From 2013 to 2017, Linda Boström Knausgård was periodically interned in a psychiatric ward where she was subjected to electroconvulsive therapy. As the treatments at this 'factory' progressed, the writer’s memories began to disappear.

After a 25-year break from boating, Brian Harvey circumnavigates Vancouver Island with his wife, his dog, and a box of documents that surfaced after his father’s death. In this memoir, Brian Harvey shares his experience of voyaging with his father’s ghost for two months in the Pacific.

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.

Manjusha Pawagi, a successful family court judge, has written a not-so-typical memoir about her experience with cancer. Wryly funny and stubbornly hopeful, this is her quirky take on what it’s like to face your own mortality when, to be honest, you thought you’d live forever. She describes how even the darkest moments of life can be made worse with roommates; details how much determination it takes to ignore the statistics; and answers the age-old question: What does it take to get a banana popsicle around here?

When her six-year-old daughter found her collapsed on the kitchen floor, Rachel had no idea how much her life was about to change. A brain scan revealed a dark shadowy mass, a huge abnormal growth of tissue that, whilst benign, was still growing and would surely kill her. It was too big to operate on. It needed to be "managed", and Rachel had, at best, two years to live. Refusing to accept the bleak prognosis, Rachel was determined to stay alive.

The word “refugee” sparks conversation and fuels emotion. There are more than 22 million refugees worldwide and another 65 million who have been forcibly displaced. But who are these people? Images filter into our consciousness via dramatic photographs - but these photos only offer a glimpse into their stories. As a young ER nurse in Boston, Roberta Gately was stopped cold by stark images of big-bellied babies with empty haunting stares in the news. She called the aid organization featured in the news story, and, within two months, she had become a humanitarian aid worker.

Citizen-Surgeon takes listeners into the otherwise inaccessible, remote, and intense world of life and surgery within a combat zone. In the backdrop of the US-led war in Afghanistan, amid a defining US Marine Corps’ offensive to conquer the Marjah region of Helmand Province, [then] US Navy Commander Paul Roach and his company-mates assemble and congeal as a medical unit in Southern California, transport from the United States to their tents in Dasht-e-Margo (the “Desert of Death”) in Helmand Province, Afghanistan.

Growing up in a New Jersey factory town in the 1980s, Daisy Hernández believed that her aunt had become deathly ill from eating an apple. No one in her family, in either the United States or Colombia, spoke of infectious diseases, and even into her 30s, she only knew that her aunt had died of a rare illness called Chagas. But as Hernández dug deeper, she discovered that Chagas - or the kissing bug disease - is more prevalent in the United States than the Zika virus.

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.

A courageous memoir that spans 40 years of Dinaaz Lentin's life experiences within our health care system. The story is raw, thought-provoking, and a brilliant look at complications and uncertainties when a medical challenge being faced is rare and uncertain. An extremely powerful example of how self-belief and trusting your own gut instinct can allow you to overcome any of life's challenges.

Echo Heron served for 18 years as a critical care nurse. In this book, she relates the true and riveting stories of nurses staff whose every-day experiences in the front line of medicine will inspire the listener.

In 1979, I was three months pregnant with my second child and in excruciating pain, pain I’d been dealing with every day for almost 15 months. I couldn’t walk, I couldn’t stand, I couldn’t sleep. It was cancer. After 40 years since diagnosis, I’m still here.... Yes, I’ve survived a lot, but I’m just like anyone else. The strength is within us all. You just have to reach for it. There is light at the end of the tunnel, even when you can’t see it. You just have to keep going, especially when it seems like you have nothing left.

In Deep Water Dream, Roedde recounts stories from her long career - from working with a Cree community in developing a medical dictionary in their own language, to training community-based health workers, to delivering Amish babies in her own home. Roedde redraws the boundaries between physician and community, strengthening the capacity to care for those close by, and offers a hopeful and powerful example to the rest of the world.

Es difícil explicar cómo la palabra cáncer puede cambiarnos la vida de una manera tan drástica. En el momento en que me diagnosticaron cáncer de seno, me sentía llena de vida; pero, sin saberlo, dentro de mi cuerpo se multiplicaba y crecía ese mal que me acercaba a la muerte.Mi lucha contra el cáncer me ha hecho una mujer más fuerte, más segura, más serena y en paz conmigo misma y con la vida.

Wondering Who You Are braids the story of Sonya and Richard's relationship and those memories he could no longer conjure together with his fateful days in the hospital and through a marriage no longer grounded on decades of shared experience.

Mark Vonnegut set out in search of Eden with his VW bug, his girlfriend, his dog, and his ideals, but genetic predisposition and a whole lot of shit going down made him crazy in a culture that told him mental illness is a myth and schizophrenia is a sane response to an insane society. Describing his experiences during the late '60s and early '70s, Eden Express reveals how Mark went from being a recent college grad who was in love and living communally on a farm to having nervous breakdowns.

Acclaimed author Peg Kehret has written the true story of the year when she was twelve and stricken with polio. At first paralyzed and terrified, she fought her way to recovery, aided by doctors and therapists, a loving family, supportive roommates fighting their own battles with the disease, and plenty of grit and luck. With the humor and suspense that are her trademarks, Peg Kehret vividly recreates a year of heartbreak and triumph.