Laurel Richardson – författare

You've finished your research and have reached the point of writing it up. You know your findings are important both for your colleagues and for a more general public. But how do you write this material to appeal to different audiences? In Writing Strategies, Laurel Richardson shows you how. Drawing on her own experiences, she carefully outlines strategies for writing up the same research in different ways. By showing the reader the stylistic and intellectual imperatives and conventions of different writing media, she prepares the writer for approaching and successfully addressing diverse audiences. From writing academic papers to trade books, from scientific writing to widely circulated work, your needs will be met using this volume as your personal guidebook. Writing Strategies will be useful to ethnographers, researchers and teachers of language and writing, and to all social scientists trying to present their material in different ways.

"There are lessons for every writer about rhetorical strategies and narrative choices. . . . She is effective in demonstrating the micro strategies of creating an authorial persona: showing how particular phrases and passages were deployed to convince the reader of the legitimacy of her text, both for the popular market and the academic one."

--Contemporary Sociology

"Excellent advice on getting started, keeping going and crafting your writing advice offered towards appropriate audiences, and much of the advice offered is as applicable to quantitative as qualitative work."

--Social Research Association News

A Story of a Marriage Through Dementia and Beyond is the extraordinary, unflinching account from sociologist Laurel Richardson of her love and caregiving through the last period of her husband Ernest Lockridge''s life - from his transient amnesia to his death from Lewy Body Dementia.

Focusing on the lived experience of the caregiver through the loved one’s journey from mild cognitive impairment to death, the book gives the reader the experience of what the medical diagnoses mean and what has led up to the loss. It shows the complex, nuanced lives of a couple both living with the worst effects of a disease like Lewy Body Dementia, while maintaining, sometimes with hope and laughter, their loving connection nourished through a 40-year marriage.

Dementia is a ‘silver tsunami’ - the third leading cause of death amongst senior populations. Richardson’s beautifully written book gives on-the-ground emotional support to those already in service as caregivers and helps prepare others for such service. Hospices, book clubs, and medical and allied professionals will find this book extraordinarily valuable. Weaving in autoethnographic and sociological methods and scholarship, as well as a list of reading and further resources for caregivers and scholars, this book will also appeal to courses in a wide range of disciplines and fields, including health communication, nursing and allied health, courses covering death and dying, end-of-life, and illness care, and, of course, scholars pursuing autoethnography, creative non-fiction, and qualitative methods.

A Story of a Marriage Through Dementia and Beyond is the extraordinary, unflinching account from sociologist Laurel Richardson of her love and caregiving through the last period of her husband Ernest Lockridge''s life - from his transient amnesia to his death from Lewy Body Dementia.

Focusing on the lived experience of the caregiver through the loved one’s journey from mild cognitive impairment to death, the book gives the reader the experience of what the medical diagnoses mean and what has led up to the loss. It shows the complex, nuanced lives of a couple both living with the worst effects of a disease like Lewy Body Dementia, while maintaining, sometimes with hope and laughter, their loving connection nourished through a 40-year marriage.

Dementia is a ‘silver tsunami’ - the third leading cause of death amongst senior populations. Richardson’s beautifully written book gives on-the-ground emotional support to those already in service as caregivers and helps prepare others for such service. Hospices, book clubs, and medical and allied professionals will find this book extraordinarily valuable. Weaving in autoethnographic and sociological methods and scholarship, as well as a list of reading and further resources for caregivers and scholars, this book will also appeal to courses in a wide range of disciplines and fields, including health communication, nursing and allied health, courses covering death and dying, end-of-life, and illness care, and, of course, scholars pursuing autoethnography, creative non-fiction, and qualitative methods.