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Relevant bibliographies by topics / Chronic illness narrative / Books

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Books on the topic 'Chronic illness narrative'

Author: Grafiati

Published: 4 June 2021

Last updated: 13 February 2022

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Consult the top 23 books for your research on the topic 'Chronic illness narrative.'

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1

Multiple voices and stories: Narratives of health and illness. Orient Blackswan, 2013.

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2

Kleinman, Arthur. The illness narratives: Suffering, healing, and the human condition. Basic Books, 1988.

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3

Duff, Kat. The alchemy of illness. Virago, 1994.

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4

Duff, Kat. The alchemy of illness. Bell Tower, 1993.

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5

Duff, Kat. The alchemy of illness. Pantheon Books, 1993.

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6

Encounters with the invisible: Unseen illness, controversy, and chronic fatigue syndrome. Southern Methodist University Press, 2005.

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7

M, Cohen Richard. Blindsided: Lifting a life above illness : a reluctant memoir. HarperCollins, 2004.

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8

The wounded storyteller: Body, illness, and ethics. University of Chicago Press, 1995.

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9

How it feels to fight for your life: The inspiring stories of fourteen children who are living with chronic illness. Simon & Schuster, 1991.

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10

A life worth living: A doctor's reflections on illness in a high-tech era. Farrar, Straus and Giroux, 2008.

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11

Krementz, Jill. How it feels to fight for your life. Joy Street Books, 1989.

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12

Krementz, Jill. How it feels to fight for your life. Little, Brown and Company, 1989.

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13

How it feels to fight for your life. Joy Street Books, 1989.

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14

Kleinman, Arthur. The Illness Narratives: Suffering, Healing, and the Human Condition. Basic Books, 1989.

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15

Linzer, Shoshana, Adina Chesir, Tal Ginsburg, and Olivia Varas. Stressful Life Events. Oxford University Press, 2017. http://dx.doi.org/10.1093/med/9780190260859.003.0005.

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Abstract:

Stressful life events often occur during the week or month preceding suicide and may aid both the formation of the suicidal narrative and the triggering of the suicide crisis syndrome. This chapter examines the stressors that have been linked to imminent suicidal behavior. The chapter has five sections. The work and career section describes imminent risk associated with economic hardship, business/work failures, and home loss. The relationship conflict section discusses suicide risks stemming from romantic rejection, intimate relationship and family conflicts, as well as abuse, neglect, and bullying. The serious medical illness section discusses suicide risks associated with diagnosis and chronicity of being critically ill. The serious mental illness section focuses on imminent risk associated with recent diagnosis, acuity and hospitalization for mental illness, as well the risks following recent failed suicide attempts. The recent substance misuse section assesses imminent risk associated with chronic alcohol/drug use, acute intoxication, and withdrawal.

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16

The Alchemy of Illness. Harmony/Bell Tower, 2000.

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17

Suffering Narratives of Older Adults: A Phenomenological Approach to Serious Illness, Chronic Pain, Recovery and Maternal Care. Taylor & Francis Group, 2014.

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18

Morrissey, Mary Beth Quaranta. Suffering Narratives of Older Adults: A Phenomenological Approach to Serious Illness, Chronic Pain, Recovery and Maternal Care. Taylor & Francis Group, 2017.

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19

Wounded Storyteller: Body, Illness, and Ethics. University of Chicago Press, 2013.

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20

The Wounded Storyteller: Body, Illness, and Ethics. University Of Chicago Press, 1997.

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21

Beyond Words Literature and Medicine. University of New Mexico Press, 2013.

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22

Wittenberg, Elaine, Joy Goldsmith, Sandra L. Ragan, and Terri Ann Parnell. Caring for the Family Caregiver. Oxford University Press, 2020. http://dx.doi.org/10.1093/med/9780190055233.001.0001.

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Abstract:

This remarkable work reveals the plight of the family caregiver in chronic illness through the prism of communication. Examining the high cost and poorly addressed exigencies of the caregiver, including health literacy, palliative care, and health outcomes, Elaine Wittenberg, Joy V. Goldsmith, Sandra L. Ragan, and Terri Ann Parnell use an interdisciplinary approach in an effort to identify the impact of communication and its burdens on the caregiver. This team of scholars present four caregiver profiles, the Manager, Carrier, Partner, and Lone caregiver, each emerging from a family system with different patterns of conversational sharing and expectations of conformity. This volume presents a picture of the costs and losses for caregivers that go unseen and remain invisible for stakeholders in the healthcare experience. By synthesizing current data assessing the experiences of caregivers, as well as integrating the narrative experiences of a range of caregivers living through a variety of illnesses and their specific demands, the writers deliver an unflinching gaze at the journey of the caregiver. With an author team comprised of three health communication researchers and a nurse and health literacy expert, this volume integrates literature addressing caregiver needs and burdens, communication theory and practice, and palliative care and health literacy research to present the groundbreaking concept of the caregiver types and an innovative set of support resources to facilitate improved pathways to better care for the caregiver. Their engaging and rigorous writing style integrates the real stories of caregivers across the scope of the book connecting the reader with the people inside the pages and making the book essential for providers, students, clinicians, policymakers, and family caregivers alike.

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23

Illness and the Limits of Expression (Conversations in Medicine and Society). University of Michigan Press, 2007.

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