Narrating Patienthood (eBook)
296 Seiten
Lexington Books (Verlag)
978-1-4985-8554-5 (ISBN)
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 ResearchChapter 3: Cultural Communication Competency as a Two-Way Street: My Journey from Medical Avoidance to Patient Self-AdvocacyChapter 4: Who will tell our stories? Emerging health legacies following the 2014-2016 Ebola EpidemicChapter 5: African Americans and Hospice Care: On Social Risk, Privacy Management, and Relational Health AdvocacyChapter 6: Can You Please Direct me to a Doctor That Has a Heart?: A Stage 4 Breast Cancer Patient NarrativeChapter 7: Exploring the Effects of Patient-Provider Communication on the Lives of Women with VulvodyniaChapter 8: Queer PatienthoodChapter 9: An Autoethnographic Account of Navigating Patienthood as a Person with Hearing ImpairmentChapter 10: From Consumer to Community-Based Researcher: Lessons from the HIV Stigma IndexChapter 11: The Gendered Nature of Generosity in Post-Hysterectomy “Dear Honey…” LettersChapter 12: The Narrative Journey and Decision-Making Process of Plastic Surgery PatienthoodChapter 13: Narrative Sense-Making in Systemic Lupus ErythematosusChapter 14: Healthy mother, healthy baby: An Autoethnography to Challenge the Dominant Cultural Narrative of the Birthing PatientChapter 15: Abelist Biases
Reihe/Serie | Lexington Studies in Health Communication |
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Co-Autor | Ashley M. Archiopoli, Crystal Daugherty, Meta Smith Davis, Patrick Dillon, Ari Hampton, Adam Hayden, Elizabeth A. Hintz, Krista Hoffman-Longtin, Alexis Zoe Johnson, Vanessa Johnson, Jody Kellas, Ann D. Bagchi, Peter M. Kellett, Andrea Meluch, Jennifer E. Ohs, Mark P. Orbe, Dwight Peavy, Rachel M. Reznik, Andrew Spieldenner, Laurel Sprague, Maria K. Venetis, Jill Yamasaki, Ambar Basu, Amanda J. Young, Russell Brewer, Gina Brown, Laura Brown, Barbara Cardell, Katherine M. Castle, Joyeeta Dastidar |
Sprache | englisch |
Themenwelt | Sachbuch/Ratgeber ► Gesundheit / Leben / Psychologie |
Geisteswissenschaften ► Sprach- / Literaturwissenschaft | |
Medizin / Pharmazie ► Gesundheitswesen | |
Naturwissenschaften | |
Sozialwissenschaften ► Kommunikation / Medien ► Kommunikationswissenschaft | |
Schlagworte | Diverse consumers • Diverse healthcare • Diverse patients • Diversity • Health • Healthcarae • Health Communication • Narrative Medicine • Patient • Patient agency • Patient Communication • Patienthood • Patient narratives |
ISBN-10 | 1-4985-8554-X / 149858554X |
ISBN-13 | 978-1-4985-8554-5 / 9781498585545 |
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