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eBook The Patient's Playbook
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Too many Americans die each year as a result of preventable medical error—mistakes, complications, and misdiagnoses. And many more of us are not receiving the best care possible, even though it’s readily available and we’re entitled to it. The key is knowing how to access it.

The Patient’s Playbook is a call to action. It will change the way you manage your health and the health of your family, and it will show you how to choose the right doctor, coordinate the best care, and get to the No-Mistake Zone in medical decision making. Leslie D. Michelson has devoted his life’s work to helping people achieve superior medical outcomes at every stage of their lives. Michelson presents real-life stories that impart lessons and illuminate his easy-to-follow strategies for navigating complex situations and cases.  

The Patient’s Playbook is an essential guide to the most effective techniques for getting the best from a broken system: sourcing excellent physicians, selecting the right treatment protocols, researching with precision, and structuring the ideal support team. Along the way you will learn:

Why having the right primary care physician will change your life

Three things you can do right now to be better prepared when illness strikes

The ten must-ask questions at the end of a hospital stay

How to protect yourself from unnecessary and dangerous treatments

Ways to avoid the four most common mistakes in the first twenty-four hours of a medical emergency

This book will enable you to become a smarter health care consumer—and to replace anxiety with confidence.




From the Hardcover edition.

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2015년 09월 01일
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Introduction
 
After I was born, in 1951, my mother went into a major postpartum depression. For the first six months of my life, she couldn’t get out of bed, leaving me in the care of my father and maternal grandmother.  I actually didn’t learn about this until I was forty-five,   and someone casually mentioned it at a party. Sadly, the stigma of psychiatric illness was so great at the time (and still can be today) that families touched by chronic depression often had to carry the burden in silence.  My parents had been counseled by doctors that they shouldn’t discuss it, so they didn’t.

My mother  eventually  recovered, but  then  she  became bipolar, which meant there were days, months,  and years when she’d be  fine,  and then long periods when she was incapable of getting up, making dinner,  or holding   a conversation. During  her manic phases, she’d be on a high  for  days or weeks, talking  nonstop  and sometimes  being cruel  to me and others  I know she loved. I couldn’t predict when her disease would take control of her. Coming home from school, I never knew if I’d be greeted by a fire-breathing dragon or a smiling mother with a glass of milk and a plate of cookies.  I had to feel around the edges of the door for danger, the way they teach you in fire safety training.

When  I was  ten,  my  mother   screamed at me  for forty-five minutes because I left  a sneaker  on the steps.  The only ten-year-old who hasn’t left a sneaker on the steps is a ten-year-old who doesn’t have sneakers or steps.

During an ugly scene when I was twelve or thirteen, I physically held my mother down in a chair and told her, “You will stop yelling at my brother right now.” That moment changed everything between us. She was my mother, and I loved her, but her disease was dangerous, and I had to be assertive.

Although my mother’s illness was hard on me, it had to have been worse for my father. The instant I was born, he lost his wife. And yet he remained extraordinarily positive and strong. He was a genuine role model, the moral center of gravity for every community that he was in—whether it was our larger family, the synagogue, the Boy Scouts, his business, or his trade association. He was the guy who would solve other people’s problems. I could talk to Dad for hours.

By my early teens, I was actively involved in helping with my mother’s care. That was when she received her first electroshock therapy treatment for recurring depression.  Later, we had her on daily lithium, a mood stabilizer. I had to grow up and become a responsible caregiver at a very young age.

And here’s where the story gets complicated. When I was in high school, my father came home one evening, clearly agitated. For me, the sun came up at night when my father walked through the door. As tired as he was, those hours with him were absolutely precious. If he came home anxious or upset, that was a big deal.

He had gone for his annual physical that day with his primary care physician, a man with   whom he’d attended high school in Newark, New Jersey. The doctor had recommended that my father see a certain cardiologist. A week or two later Dad came home even more rattled than before.  The cardiologist had told him he needed to have open-heart surgery.

I was overcome with worry. Was my dad going to die? Losing him wouldn’t just mean I’d  be an orphan,  practically  speaking; it would mean I’d  have to take full responsibility  for my mother. That was not a reality I could handle.

That night I couldn’t sleep. The next day I couldn’t concentrate at sc

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