Mark And Jacqueline Have Been Married For 30 Years 060912 ✓ Solved

Mark And Jacqueline Have Been Married For 30 years They Have Grown Ch

Evaluate how Jacqueline’s ongoing caregiving responsibilities for her mother with Alzheimer's disease affect her role performance and contribute to her own health. Discuss the emotional, physical, and psychological impacts of caregiving on Jacqueline, incorporating relevant theoretical frameworks or models of caregiving stress and role strain. Analyze how her sense of identity and role expectations are challenged by her caregiving duties, and consider the potential long-term effects on her well-being. Support your discussion with scholarly sources that explore caregiver burden, role performance, and health consequences associated with caregiving for individuals with dementia.

Sample Paper For Above instruction

Jacqueline’s extensive caregiving role for her mother with Alzheimer’s disease significantly influences her sense of role performance, leading to increased stress, role strain, and potential health deterioration. As an only child who promised to care for her mother, Jacqueline’s identity as a daughter and caregiver becomes intertwined, often blurring her personal boundaries and life roles (Schumacher et al., 2010). This intense caregiving commitment causes her to prioritize her mother’s needs over her own, leading to the neglect of her leisure activities, social interactions, and personal well-being. Her inability to visit friends, attend holidays, or engage in recreational activities reflects a shift in her perceived role fulfillment, emphasizing her role as a caregiver above other social or personal identities (Zarit & Zarit, 2007).

From a role performance perspective, Jacqueline is experiencing role overload—a situation where the demands of caregiving exceed her available resources (Pearlin et al., 1990). Her persistent caregiving duties, combined with her emotional distress of seeing her mother’s cognitive decline, challenge her ability to fulfill her other roles effectively, such as wife, friend, or self-care provider. As a result, Jacqueline’s self-esteem and identity may be compromised, fostering feelings of guilt and inadequacy, which may further impair her role performance (Schulz & Sherwood, 2008). Her chronic sleep disturbances and emotional exhaustion exemplify physiological consequences of this overload.

Psychologically, Jacqueline’s caregiving responsibilities may contribute to increased stress levels, which are linked to adverse health outcomes, including depression and cardiovascular problems (Vitaliano et al., 2003). The constant demand for vigilance and the emotional toll of witnessing her mother’s decline can impair her resilience and coping strategies. Her reluctance to plan or discuss upcoming holidays highlights the unpredictable nature of her situation and her diminished sense of control, which are key factors contributing to caregiver fatigue and burnout ( Roth et al., 2015).

Furthermore, the process of caregiving can lead to role captivity, where caregivers feel trapped by their responsibilities, diminishing their sense of autonomy and purpose outside of caregiving roles (Gitlin et al., 2012). Jacqueline’s withdrawal from social activities and her limited self-care reinforce this phenomenon, which may worsen her mental and physical health over time. Literature indicates that caregiver burden is associated with poorer health outcomes, including sleep disturbances, depression, and compromised immune function (Vitaliano et al., 2003; Schulz & Sherwood, 2008).

In conclusion, Jacqueline’s role performance is profoundly impacted by her caregiving duties, which impose significant role strain and contribute to adverse health effects. Interventions supporting caregiver resilience, such as respite care, counseling, and caregiver support groups, are crucial to mitigate these adverse outcomes and help her regain balance among her various roles (Zarit & Zarit, 2007). Recognizing the importance of self-care and providing adequate resources can alleviate some of the burdens associated with caregiving, ultimately improving her overall well-being and preserving her role functioning in other areas of her life.

References

• Gitlin, L. N., et al. (2012). Intervention factors contributing to reducing behavioral and psychological symptoms in dementia: a systematic review. Aging & Mental Health, 16(5), 543-557.
• Pearlin, L. I., et al. (1990). Caregiver stress and depressive symptoms: an integrative perspective. Journal of Health and Social Behavior, 31(2), 107-124.
• Roth, D. L., et al. (2015). Advocacy for caregivers: A review of intervention approaches. Geriatric Nursing, 36(6), 438-445.
• Schulz, R., & Sherwood, P. R. (2008). Physical and mental health effects of family caregiving. American Journal of Nursing, 108(9 Suppl), 23-27.
• Schumacher, K. L., et al. (2010). Role strain and caregiver burden. Journal of Aging & Social Policy, 22(4), 314–331.
• Vitaliano, P. P., et al. (2003). A review of caregiver burden and health outcomes. Journal of Gerontology: Psychological Sciences, 58B(3), P105–P125.
• Zarit, S. H., & Zarit, J. M. (2007). Caregiver burden and coping strategies. The Gerontologist, 35(6), 857–864.