Details
Narrating Patienthood
Engaging Diverse Voices on Health, Communication, and the Patient ExperienceLexington Studies in Health Communication
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36,99 € |
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| Verlag: | Lexington Books |
| Format: | EPUB |
| Veröffentl.: | 26.11.2018 |
| ISBN/EAN: | 9781498585545 |
| Sprache: | englisch |
| Anzahl Seiten: | 296 |
DRM-geschütztes eBook, Sie benötigen z.B. Adobe Digital Editions und eine Adobe ID zum Lesen.
Beschreibungen
<span>Diversity plays an important role in how people experience illness and healthcare as patients. Listening carefully to stories of how race, class, age, gender, sexuality, and disability can affect patient experience can be revealing and provide much needed change to health communication in the patienthood narrative. This book is a collection of vibrant and engaging essays by scholars of narrative methods in health communication. Each chapter takes readers into the fascinating world of patients who use stories from their personal lives to challenge us to rethink, reimagine, and reformulate what health communication means in practice. <br><br>Each section of the book focuses on an important aspect of the theory and practice of the patienthood narrative. Part one explores the important ways that telling and sharing patient’s stories can lead to learning, empowerment, and advocacy. Part two explores several key forms of diversity and how they affect patienthood. Part three illustrates how personal, relational, and cultural aspects of identity intersect to shape the patient experience. </span>
<span>Engaging the reader with a variety of patient narratives and health communication scholarship, this book illustrates how narratives can create change; how differences matter; and how identity, relational, and cultural factors intersect to affect patienthood.</span>
<span>Chapter 1: Narrating Patient Experience: Benefits for multiple audiences </span>
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<br>
<span>Chapter </span>
<span>2</span>
<span>: </span>
<span>From Stories to Discoveries: Patients’ Narratives as Advocacy in Biomedical Research</span>
<br>
<br>
<span>Chapter 3: Cultural Communication Competency as a Two-Way Street: My Journey from Medical Avoidance to Patient Self-Advocacy</span>
<br>
<br>
<span>Chapter 4: Who will tell our stories? Emerging health legacies following the 2014-2016 Ebola Epidemic</span>
<br>
<br>
<span>Chapter 5: African Americans and Hospice Care: On Social Risk, Privacy Management, and Relational Health Advocacy</span>
<br>
<br>
<span>Chapter 6: Can You Please Direct me to a Doctor That Has a Heart?: A Stage 4 Breast Cancer Patient Narrative</span>
<br>
<br>
<span>Chapter 7: </span>
<span>Exploring the Effects of Patient-Provider Communication on the Lives of Women with Vulvodynia</span>
<br>
<br>
<span>Chapter 8: Queer Patienthood</span>
<br>
<br>
<span>Chapter 9: An Autoethnographic Account of Navigating Patienthood as a Person with Hearing Impairment</span>
<br>
<br>
<span>Chapter 10: From Consumer to Community-Based Researcher: Lessons from the HIV Stigma Index</span>
<br>
<br>
<span>Chapter 11: The Gendered Nature of Generosity in Post-Hysterectomy “Dear Honey…” Letters</span>
<br>
<br>
<span>Chapter 12: The Narrative Journey and Decision-Making Process of Plastic Surgery Patienthood</span>
<br>
<br>
<span>Chapter 13: Narrative Sense-Making in Systemic Lupus Erythematosus</span>
<br>
<br>
<span>Chapter 14: Healthy mother, healthy baby: An Autoethnography to Challenge the Dominant Cultural Narrative of the Birthing Patient</span>
<br>
<br>
<span>Chapter 15: Abelist Biases</span>
<br>
<br>
<span>Chapter </span>
<span>2</span>
<span>: </span>
<span>From Stories to Discoveries: Patients’ Narratives as Advocacy in Biomedical Research</span>
<br>
<br>
<span>Chapter 3: Cultural Communication Competency as a Two-Way Street: My Journey from Medical Avoidance to Patient Self-Advocacy</span>
<br>
<br>
<span>Chapter 4: Who will tell our stories? Emerging health legacies following the 2014-2016 Ebola Epidemic</span>
<br>
<br>
<span>Chapter 5: African Americans and Hospice Care: On Social Risk, Privacy Management, and Relational Health Advocacy</span>
<br>
<br>
<span>Chapter 6: Can You Please Direct me to a Doctor That Has a Heart?: A Stage 4 Breast Cancer Patient Narrative</span>
<br>
<br>
<span>Chapter 7: </span>
<span>Exploring the Effects of Patient-Provider Communication on the Lives of Women with Vulvodynia</span>
<br>
<br>
<span>Chapter 8: Queer Patienthood</span>
<br>
<br>
<span>Chapter 9: An Autoethnographic Account of Navigating Patienthood as a Person with Hearing Impairment</span>
<br>
<br>
<span>Chapter 10: From Consumer to Community-Based Researcher: Lessons from the HIV Stigma Index</span>
<br>
<br>
<span>Chapter 11: The Gendered Nature of Generosity in Post-Hysterectomy “Dear Honey…” Letters</span>
<br>
<br>
<span>Chapter 12: The Narrative Journey and Decision-Making Process of Plastic Surgery Patienthood</span>
<br>
<br>
<span>Chapter 13: Narrative Sense-Making in Systemic Lupus Erythematosus</span>
<br>
<br>
<span>Chapter 14: Healthy mother, healthy baby: An Autoethnography to Challenge the Dominant Cultural Narrative of the Birthing Patient</span>
<br>
<br>
<span>Chapter 15: Abelist Biases</span>
<span>Peter M. Kellett</span>
<span> is associate professor of communication studies at University of North Carolina at Greensboro. </span>
<span> is associate professor of communication studies at University of North Carolina at Greensboro. </span>
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