作品简介

　　生活中的变故扑面而来，该如何面对？

　　“阿尔茨海默病”会选择什么样的患者？——无差别选择。

　　“阿尔茨海默病患者”会有怎么样的人生？——由照护者决定。

　　“阿尔茨海默病患者的照护者”又会选择怎样的生活？——等“我”成为照护者的那天再回答吧。

　　它不是“苦难文学”，阅读它不需要笑中带泪；它不是“照护指南”，无需认真记录；它是“朋友讲述的故事”，只需倾听。

　　“高尚从来不是我的目的，成为一名照护者也不曾是我的初衷，但当所爱之人患上不治之症，我责无旁贷地挑起了这副重担。我是阿尔茨海默病先生的妻子——蓝江。”

　　这是一本记录了九年婚姻时光的书，这段时光是阿尔茨海默病患者的妻子的九年。

　　阿尔茨海默病，这是一个残酷的诊断，它预示了一个漫长而痛苦的过程。这个诊断是一个诅咒，不仅病人自己，还有病人的家人和朋友，都将沦为“受害者”。他们将被迫目睹病人的病情日趋恶化，被迫目睹爱人在痛苦中挣扎却无能为力，同时，他们还要承担起越来越沉重的照护责任。

　　作者蓝江是美国一所大学的教授，某天在大学担任董事会顾问的丈夫克拉德被确诊患上阿尔茨海默病。在此后九年对丈夫的照护生活中，她用爱作支撑，用智慧找方向，用温柔和幽默面对未知，以她“中西并用”的独特方式拥抱生活，在严峻环境中顽强挣扎，最终找到一条适合自己的照护之路。

　　蓝江，上海人，祖籍浙江奉化。1969年赴内蒙古自治区插队落户，1976年毕业于内蒙古师范学院英语专业，从事英语教育。1986年求学美国，1993年获教育技术（Instructional Technology）博士学位后，辗转于美国东南西北，曾任IT管理人员，多所大学终身教授，及多个美国教育组织董事会成员。2011年辞职，定居美国西雅图。

　　著有多篇学术论文，本书为第一部非学术作品，英文版（Well Spouse:Love,Resilience,and Alzheimer’s）2020年9月在美国出版。

Introduction of works

How to face the changes in life?

What kind of patients will Alzheimer's Disease choose? -- Indiscriminate choice.

What is the life of an Alzheimer's patient? - At the discretion of the caregiver.

What kind of life will "caregivers of Alzheimer's patients" choose? - Wait until the day "I" become a caregiver.

It is not "the literature of suffering," and you do not need to laugh and cry to read it; It is not a "care guide" and does not require careful recording; It's "a story told by a friend," just listen.

"Being noble was never my purpose, and being a caregiver was never my original intention, but when a loved one became terminally ill, I was duty-bound to carry the burden." I'm Mr. Alzheimer's wife -- Langjiang."

It's a book that Chronicles nine years of marriage, nine years of the wife of an Alzheimer's patient.

Alzheimer's disease, it's a brutal diagnosis, and it foreshadows a long and painful process. This diagnosis is a curse, not only the patient himself, but also the patient's family and friends, will become "victims." They will be forced to watch their patients deteriorate, to watch their loved ones struggle in pain, and to take on an increasingly heavy burden of care.

The author is a professor at a university in the U.S., and one day her husband Krader, who is an advisor to the board of directors of the university, was diagnosed with Alzheimer's disease. In the following nine years of her husband's care life, she used love as support, found the direction with wisdom, faced the unknown with gentleness and humor, embraced life in her unique way of "both Chinese and western", struggled stubbornly in the severe environment, and finally found a suitable way for her own care.

Lanjiang, Shanghai native, Zhejiang Fenghua. In 1969, he went to Inner Mongolia Autonomous Region and settled down. In 1976, he graduated from Inner Mongolia Normal College, majoring in English, and engaged in English education. He studied in the United States in 1986 and received his Ph.D. in Instructional Technology in 1993. After moving around the United States, he worked as an IT administrator, tenured professor at several universities, and board member of several educational organizations in the United States. He resigned in 2011 and settled in Seattle, USA.

How academic papers, book for the first academic works, the English version (Well Spouse: Love, Resilience, and Alzheimer 's) published in America in September 2020.