Impact of Emotional and Psychological Factors on Illness Outcomes
Order Instructions
SOCIAL WORK
SOCW 6205 – MEDICAL SOCIAL WORK II
Discussion 2: Impact of Emotional and Psychological Factors on Illness Outcomes
The experience of illness can reach beyond the patient and impact the family system considerably. Patients experience illness through the lenses of their personal emotions, past experiences, stage of life, familial role, social relationships, responsibilities, stressors, and cultural and spiritual beliefs. Other factors, including the nature of the illness and comorbid conditions, also influence how the patient perceives illness. Together, these factors impact how and whether patients seek care, utilize health resources, and receive and adhere to treatment—all of which eventually impact the outcome of the illness.
To prepare for this Discussion:
Think about a patient’s emotional or psychological response to illness and the factors (e.g., depression, stress, anxiety) that might contribute to this response. Select two factors that you believe are important and might critically affect a patient’s course of life beyond family (e.g., at work, school, social life, role in the community). Consider the stages of an illness—diagnosis, treatment, adherence to treatment, worsening of condition, complications, and survival.
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• By Day 3 (Note!!! PLEASE WRITE OUT EACH QUESTION BEFORE PROVIDING A RESPONSE. “Please I need an excellent paper”
Post a description of the two factors you selected. Explain how these factors influence illness and a patient’s life beyond his or her family. Then, explain how these factors might present themselves during at least two stages during the course of illness. Finally, explain how a medical social worker might intervene to ensure that the patient receives the services he or she needs to cope best during each of these stages.
Be sure to support your responses with specific references to the resources. If you are using additional articles, be sure to provide full APA-formatted citations for your references both within the text and on the referencing section. PLEASE ALWAYS INCLUDE THE REQIRED TEXTBOOK as part of the references and if possible some of the REQUIRED READING if applicable. Please always start by referring to THE TEXTBOOK, below
REQUIRED TEXTBOOK
Hospital Social Work 2006
Author: Beder, Joan
ISBN-13: 978-0-415-95067-1
ISBN-10: 0-415-95067-8
Edition/Copyright: 2006
Publisher: Routledge N. Y.
REQUIRED
Handbook of Health Social Work 3RD 19
Author: Gehlert, Sarah
ISBN-13: 978-1-119-42072-9
ISBN-10: 1-119-42072-5
Edition/Copyright: 3RD 19
Publisher: John Wiley & Sons, Inc.
REQUIRED
Social Work in Health Settings: Practice in Context 4TH 16
Author: McCoyd, Judith L.M.
ISBN-13: 978-1-138-92436-9
ISBN-10: 1-138-92436-9
Edition/Copyright: 4TH 16
Publisher: Routledge N. Y.
Required Readings
Chiang, J.J., Miller, G. E., Turiano, N.A., Mroczek, D.K. (2018). Affective reactivity to daily stress and 20-year mortality risk in adults with chronic illness: Findings from the national study of daily experiences. Health Psychology, 37(2), 170-178.
Martire, L. M., & Schulz, R. (2007). Involving family in psychosocial interventions for chronic illness. Current Directions in Psychological Science, 16(2), 90–94.
Petrie, K. J., & Weinman, J. (2012). Patients’ perceptions of their illness: The dynamo of volition in health care. Current Directions in Psychological Science, 21(1), 60– 65.
Goldberg, A., & Rickler, K. S. (2011). The role of family caregivers for people with chronic illness. Medicine and Health, Rhode Island, 94(2), 41–42. Retrieved from http://www.rimed.org/medhealthri/2011-02/2011-02- 41.pdf
The Role of Family Caregivers for People with Chronic Illness by Goldberg, A.; Rickler, K. S., in Medicine and Health, Rhode Island, Vol. 94/Issue 2. Copyright 2011 by Rhode Island Medical Society. Reprinted by permission of Rhode Island Medical Society.
Karelina, K., & DeVries, A. C. (2011). Modeling social influences on human health. Psychosomatic Medicine, 73(1), 67–74.
Modeling social influences on human health by Karelina, K., & DeVries, A. C., in Psychosomatic Medicine, Vol. 73, Issue 1. Copyright 2011 by Lippincott Williams & Wilkins, Inc. Reprinted by permission of Lippincott Williams & Wilkins, Inc. via the Copyright Clearance Center.
Lawrence, E. (2012). The impact of chronic illness on the family. Retrieved from http://www.igliving.com/magazine/articles/IGL_2012-06_AR_The-Impact-of-Chronic-Illness-on-the-Family.pdf
Lawrence, E. (2012). The impact of chronic illness on the family. Used with permission of FFF Enterprises, Inc. Retrieved from http://www.igliving.com/Assets/IGL/Articles/IGL_2012-06_AR_The-Impact-of-Chronic-Illness-on-the-Family.pdf
Conrad, P., & Barker, K. K. (2010). The social construction of illness: Key insights and policy implications. Journal of Health and Social Behavior, 51(S1), S67–S79.
Uchino, B. N. (2009). Understanding the links between social support and physical health: A life-span perspective with emphasis on the separability of perceived and received support. Perspectives on Psychological Science, 4(3), 236–255.
Optional Resources
Northouse, L., Williams, A. L., Given, B., & McCorkle, R. (2012). Psychosocial care for family caregivers of patients with cancer. Journal of Clinical Oncology, 30(11), 1227–1234.
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