Narrating Patienthood

Narrating Patienthood
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Engaging Diverse Voices on Health, Communication, and the Patient Experience
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Artikel-Nr:
9781498585545
Veröffentl:
2018
Seiten:
296
Autor:
Ashley M. Archiopoli
Serie:
Lexington Studies in Health Communication
eBook Typ:
EPUB
Kopierschutz:
Adobe DRM [Hard-DRM]
Sprache:
Englisch
Beschreibung:

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.
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.

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.
Chapter 1: Narrating Patient Experience: Benefits for multiple audiences

Chapter 2: From Stories to Discoveries: Patients’ Narratives as Advocacy in Biomedical Research

Chapter 3: Cultural Communication Competency as a Two-Way Street: My Journey from Medical Avoidance to Patient Self-Advocacy

Chapter 4: Who will tell our stories? Emerging health legacies following the 2014-2016 Ebola Epidemic

Chapter 5: African Americans and Hospice Care: On Social Risk, Privacy Management, and Relational Health Advocacy

Chapter 6: Can You Please Direct me to a Doctor That Has a Heart?: A Stage 4 Breast Cancer Patient Narrative

Chapter 7: Exploring the Effects of Patient-Provider Communication on the Lives of Women with Vulvodynia

Chapter 8: Queer Patienthood

Chapter 9: An Autoethnographic Account of Navigating Patienthood as a Person with Hearing Impairment

Chapter 10: From Consumer to Community-Based Researcher: Lessons from the HIV Stigma Index

Chapter 11: The Gendered Nature of Generosity in Post-Hysterectomy “Dear Honey…” Letters

Chapter 12: The Narrative Journey and Decision-Making Process of Plastic Surgery Patienthood

Chapter 13: Narrative Sense-Making in Systemic Lupus Erythematosus

Chapter 14: Healthy mother, healthy baby: An Autoethnography to Challenge the Dominant Cultural Narrative of the Birthing Patient

Chapter 15: Abelist Biases

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