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Книги з теми "Cancer caregiving"

Щоб переглянути інші типи публікацій з цієї теми, перейдіть за посиланням: Cancer caregiving.

Автор: Grafiati

Опубліковано: 10 грудня 2022

Оновлено: 29 січня 2023

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1

Talley, Ronda C., Ruth McCorkle, and Walter F. Baile, eds. Cancer Caregiving in the United States. New York, NY: Springer New York, 2012. http://dx.doi.org/10.1007/978-1-4614-3154-1.

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2

Pebbling the walk: Surviving cancer caregiving. Portland, Or: Blue Heron Publishing, 2000.

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3

Houts, Peter S., Julia A. Bucher, and Terri B. Ades. American Cancer Society complete guide to family caregiving: The essential guide to cancer caregiving at home. 2nd ed. Atlanta, Ga: American Cancer Society/Health Promotions, 2011.

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4

Bucher, Julia A. American Cancer Society's Complete Guide To Family Caregiving, Second Edition: The Essential Guide T. S.l: American Cancer Society, 2008.

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5

Woznick, Leigh A. Living with childhood cancer. Washington, DC: American Psychological Association, 2002.

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6

Esther, Sales, Schulz Richard 1947-, and Mandel School of Applied Social Sciences (Case Western Reserve University), eds. Family caregiving in chronic illness: Alzheimer's disease, cancer, heart disease, mental illness, and stroke. Newbury Park, Calif: Sage Publications, 1991.

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7

Lioness, Ayres, ed. Stories of family caregiving: Reconsiderations of theory, literature, and life. Indianapolis, IN: Center Nursing Pub., 2002.

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8

Help me live: 20 things people with cancer want you to know. Berkeley: Celestial Arts, 2011.

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9

American Cancer Society. Cancer Caregiving A-Z. American Cancer Society, 2008.

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10

Houts, Peter S. Caregiving. 2nd ed. American Cancer Society, 2003.

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11

Cancer Caregiving in the United States Caregiving Research Practice Policy. Springer, 2012.

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12

Olson, Rebecca E. Towards a Sociology of Cancer Caregiving. Taylor & Francis Group, 2020.

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13

Olson, Rebecca E. Towards a Sociology of Cancer Caregiving. Routledge, 2016. http://dx.doi.org/10.4324/9781315550619.

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14

Houts, Peter, and Julia Bucher. American Cancer Society Complete Guide to Family Caregiving: The Essential Guide to Cancer Caregiving at Home. American Cancer Society, Incorporated, 2012.

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15

Houts, Peter, and Julia Bucher. American Cancer Society Complete Guide to Family Caregiving: The Essential Guide to Cancer Caregiving at Home. American Cancer Society, Incorporated, 2012.

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16

Towards a Sociology of Cancer Caregiving: Time to Feel. Taylor & Francis Group, 2015.

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17

Houts, Peter S., and Julia Bucher. American Cancer Society Complete Guide to Family Caregiving. 2nd ed. American Cancer Society, 2008.

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18

Cancer Caregiving in the United States: Research, Practice, Policy. Springer, 2012.

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19

Cancer Caregiving in the United States: Research, Practice, Policy. Springer, 2014.

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20

Olson, Rebecca E. Towards a Sociology of Cancer Caregiving: Time to Feel. Taylor & Francis Group, 2016.

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21

Olson, Rebecca E. Towards a Sociology of Cancer Caregiving: Time to Feel. Taylor & Francis Group, 2016.

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22

Olson, Rebecca E. Towards a Sociology of Cancer Caregiving: Time to Feel. Taylor & Francis Group, 2016.

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23

Dickson, Kenneth. Living Through Cancer: A Story of Love and Caregiving. Trafford Publishing, 2005.

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24

Dickson, Kenneth. Living Through Cancer: A Story of Love and Caregiving. Trafford Publishing, 2005.

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25

Barry, Michael S. The Art of Caregiving: How to Lend Support & Encouragement to Those With Cancer. Life Journey, 2007.

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26

Boehmer, Ulrike, Melissa A. Clark, and Lisa Fredman. Female Caregivers to Female Cancer Survivors (DRAFT). Edited by Youngmee Kim and Matthew J. Loscalzo. Oxford University Press, 2018. http://dx.doi.org/10.1093/med/9780190462253.003.0005.

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Анотація:

In this chapter, the authors focus on adult female caregivers performing informal caregiving tasks to adult females diagnosed with cancer. The authors limit discussion to a binary definition of gender, whereas Chapter 11 addresses gender minorities, including transwomen caregivers and transgender care recipients. The authors present national data on adult caregivers and describe the characteristics of female-to-female caregivers. They present a theoretical model for evaluating the impact of female-to-female cancer caregiving and review interventions that are relevant to this group of caregivers. While female caregiver to female patient is the most prevalent caregiver–patient combination, there is mostly an absence of same-gender effects on cancer caregiving and interventions.

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27

Dickson, Kenneth. Living Through Cancer: A Story of Love and Caregiving Plus Workbook. Trafford Publishing, 2005.

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28

Barry, Michael S. Art of Caregiving: How to Lend Support and Encouragement to Those with Cancer. Cook, David C., 2015.

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29

Barry, Michael S. Art of Caregiving: How to Lend Support and Encouragement to Those with Cancer. Cook, David C., 2015.

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30

Society, American Cancer, ed. Cancer caregiving A to Z: An at-home guide for patients and families. Atlanta, GA: American Cancer Society/Health Promotions, 2008.

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31

Cancer caregiving A to Z: An at-home guide for patients and families. Atlanta, GA: American Cancer Society/Health Promotions, 2008.

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32

Sparks, Tracy M. Helping Your Spouse Beat Stage IV Cancer: The Never-Ending Cycle to Caregiving. Independently Published, 2020.

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33

Applebaum, Allison J., ed. Cancer Caregivers. Oxford University Press, 2019. http://dx.doi.org/10.1093/med/9780190868567.001.0001.

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Анотація:

Cancer caregivers are an essential extension of the healthcare team. Rapid advances in cancer care, including new drugs and immunotherapies and more sophisticated diagnostic tools, have improved our ability to extend lives and enhance survival. As patients are living longer and with today’s shorter hospital stays and shift towards increased outpatient care, however, the burden on caregivers and their needs have substantially increased. Cancer Caregivers reveals the depth of complexities of caregiving experiences that the field of Psycho-Oncology has been exploring and the vast expanses we have left to understand. This text describes the characteristics and experiences of cancer caregivers based on their life stage, relationship to the patient, and ethnic group membership, as well as patients’ disease and treatment type. It highlights the significant progress in research focused on the development and dissemination of psychosocial interventions for cancer caregivers, and includes in-depth case studies to illustrate their delivery and application. The text also explores the provision of support to caregivers in the community and the legal and ethical concerns faced by caregivers across the care trajectory. Cancer Caregivers offers both fundamental and practical information and is a resource for all healthcare professionals who work with patients and families facing cancer.

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34

Stetz, Kathleen Mary. THE EXPERIENCE OF SPOUSE CAREGIVING FOR PERSONS WITH ADVANCED CANCER (FAMILY, COPING, CHRONIC ILLNESS). 1986.

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35

(Editor), Peter S. Houts, and Julia A. Bucher (Editor), eds. Caregiving: A Step-By-Step Resource for Caring for People With Cancer at Home. American Cancer Society, 2000.

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36

Ayres, Lioness, and Lioness Ph D. Ayres. Stories of Family Caregiving: Reconsiderations of Theory, Literature, And Life. SIGMA Theta Tau International, Center for Nur, 2002.

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37

S, Houts Peter, Bucher Julia A, Nezu Arthur M, and American Cancer Society, eds. Caregiving: A step-by-step resource for caring for the person with cancer at home. [S.l.]: American Cancer Society, 2000.

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38

Sivaram, Sudha. Cancer in the Global Health Context. Edited by David A. Chambers, Wynne E. Norton, and Cynthia A. Vinson. Oxford University Press, 2018. http://dx.doi.org/10.1093/med/9780190647421.003.0029.

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Globally, a shift in the pattern of disease from infectious etiology to chronic conditions is leading to an increased focus on the prevention and control of non-communicable diseases. In this chapter, three cases are presented that illustrate the potential of implementation science in low- and middle-income countries. The first is a case from India that seeks to understand the context of care seeking and caregiving for cervical cancer in India. The second case presents more than a decade of work in El Salvador, a country with competing priorities in health. The third case describes how implementation science methods are being used in Vietnam to identify barriers to and facilitators for implementing a tobacco cessation intervention in community settings.

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39

Blank, Thomas O., Lara Descartes, and Marysol Asencio. Male Patients and Their Male Caregivers (DRAFT). Edited by Youngmee Kim and Matthew J. Loscalzo. Oxford University Press, 2018. http://dx.doi.org/10.1093/med/9780190462253.003.0006.

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There is a dearth of literature on male-to-male caregiving relationships generally and almost none specific to cancer. Some prior studies have included male caregivers and/or male care recipients, but they have rarely separated out male–male dyads for analysis. Thus, without access to much research specific to male–male caregiving for cancer, this chapter draws on related and relevant literature, such as that on men caring for men with AIDS and interactions within prostate cancer support groups. These findings are used to describe what male–male caregiving may look like. A consideration of how female caregiving is typically foregrounded and valued in the caregiving literature is used to critique the current state of knowledge of male caregiving, and the large research gap in this field is identified.

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40

Snoad, John, and Sherri Snoad. Welcome to the Other Side!: Reclaiming Life after Surviving and Caregiving Through the Abyss of Cancer. Author Solutions, Incorporated, 2021.

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41

Snoad, John, and Sherri Snoad. Welcome to the Other Side!: Reclaiming Life after Surviving and Caregiving Through the Abyss of Cancer. Author Solutions, Incorporated, 2021.

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42

Snoad, John, and Sherri Snoad. Welcome to the Other Side!: Reclaiming Life after Surviving and Caregiving Through the Abyss of Cancer. Author Solutions, Incorporated, 2021.

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43

Kim, Youngmee, Hannah-Rose Mitchell, and Amanda Ting. Theories of Gender in Adjustment to Medical Illness (DRAFT). Edited by Youngmee Kim and Matthew J. Loscalzo. Oxford University Press, 2018. http://dx.doi.org/10.1093/med/9780190462253.003.0003.

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Caregiving has historically been considered the role of women, yet the number of male caregivers has increased substantially in recent years. Such changes call for systematic understanding of the role of gender in caregiving processes. This chapter summarizes theoretical perspectives pertaining to gender issues in caregiving and then evaluates their adequacy for the cancer caregiver population. Despite lack of gender theory–driven research in cancer caregiving, studies support the adequacy of gender theories in identifying subgroups of caregivers who are vulnerable to adverse effects of cancer in the family and in developing evidence-based interventions. Integration of the issues related to the medical trajectory of the patients, lifespan stage of the caregivers, sociocultural resources, and risk factors in this emerging area of gender-oriented research and practice in cancer caregiver is highly encouraged.

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44

Applebaum, Allison J. Meaning-Centered Psychotherapy for Cancer Caregivers. Oxford University Press, 2017. http://dx.doi.org/10.1093/med/9780199837229.003.0006.

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Existential distress among caregivers of patients with all sites and stages of cancer is common and may serve as a driving mechanism of caregiver burden. Concurrently, the caregiving experience is an opportunity for meaning-making and growth. To date, no empirically supported treatments specifically target meaning-making and existential distress among cancer caregivers. To address this critical gap in the literature, meaning-centered psychotherapy has been adapted for delivery to cancer caregivers (meaning-centered psychotherapy for cancer caregivers (MCP-C)). This chapter presents the rationale and overview of MCP-C, and it highlight key elements of the intervention that uniquely target the specific existential needs of cancer caregivers. A case example of an MCP-C group member is presented to illustrate key MCP-C therapeutic techniques. It also discusses challenges of delivery of MCP-C to this vulnerable population and current MCP-C trials that address these barriers to delivery and utilization.

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45

KENT, James. Complete Colorectal Cancer Cookbook: Nutritious Recipes to Fight Colon Rectum Includes Prevention, Therapies, Caregiving and Much More. Independently Published, 2022.

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46

Hagedoorn, Mariët, and Tracey A. Revenson. Men Caring for Women in the Cancer Context (DRAFT). Edited by Youngmee Kim and Matthew J. Loscalzo. Oxford University Press, 2018. http://dx.doi.org/10.1093/med/9780190462253.003.0004.

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Анотація:

This chapter provides an overview of the consequences of a cancer diagnosis for female patients and their male caregivers, mostly partners or spouses. The majority of the couples adjust well; only a minority shows elevated levels of psychological distress a year or more after diagnosis. Nevertheless, the literature shows that cancer and its treatment may have a considerable impact on sexual functioning, fertility, and other aspects of the relationship. Communication between patients and partners and between couples and health care professionals plays a key role in solutions to these problems. Psychosocial interventions that may ameliorate the stresses these couples face are presented throughout the chapter. The authors also address issues of gender and caregiving.

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47

Shapiro, Dan. And in health: A guide for couples facing cancer together. 2013.

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48

McQuellon, Richard P., and Michael A. Cowan. The Art of Conversation in Cancer Care. 2nd ed. Oxford University Press, 2021. http://dx.doi.org/10.1093/med/9780197500293.001.0001.

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The Art of Conversation in Cancer Care: Lessons for Caregivers, is organized around the themes of mortal time and healing conversation with patients and their caregivers. Mortal time is not so much a specific period, but rather, the psychological experience encountering mortality that accompanies the diagnosis of cancer. The book has three major sections. In part I, the many ways people experience mortal time are articulated. These include a range of adaptive and less adaptive methods such as dysfunctional avoidance. In part II, the basic elements of healing conversation are described, with an emphasis on the hope that can spring from talking with a trusted companion. We discuss empathy, listening carefully and responding thoughtfully and compassionately. In Part III, the topic is guidance for caregivers. This section includes material on the risks and costs of caregiving as well as personal virtues that help a person navigate the demands of mortal time with their loved one. We discuss resilience and the consequences of absorbing suffering including empathy shift where the cancer caregiver becomes less empathic with minor illnesses in others. We conclude with the power of healing conversation in mortal time as a source of hope. The book includes numerous patient vignettes that illustrate the art of conversation in cancer medicine.

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49

Damocles Wife The Inside Story Of Cancer Caregiving Longterm Survival In The Midst Of Motherhood Marriage Making Life Matter. Two Louise Press, 2012.

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50

Woznick, Leigh A., and Carol D. Goodheart. Living With Childhood Cancer : A Practical Guide to Help Families Cope. American Psychological Association (APA), 2001.

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