Narrating Patienthood

Narrating Patienthood

Engaging Diverse Voices on Health, Communication, and the Patient Experience
Buch | Hardcover
296 Seiten
2018
Lexington Books (Verlag)
978-1-4985-8553-8 (ISBN)
123,45 inkl. MwSt
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.

Peter M. Kellett is associate professor of communication studies at University of North Carolina at Greensboro.

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

Erscheinungsdatum
Reihe/Serie Lexington Studies in Health Communication
Co-Autor Ashley M. Archiopoli, Ann D. Bagchi, Ambar Basu, Russell Brewer, Gina Brown
Verlagsort Lanham, MD
Sprache englisch
Maße 161 x 229 mm
Gewicht 581 g
Themenwelt Sachbuch/Ratgeber Gesundheit / Leben / Psychologie
Medizin / Pharmazie Gesundheitswesen
Sozialwissenschaften Kommunikation / Medien Kommunikationswissenschaft
ISBN-10 1-4985-8553-1 / 1498585531
ISBN-13 978-1-4985-8553-8 / 9781498585538
Zustand Neuware
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