Case Study: Family Member With Alzheimer's Disease Ma 343137
Case Study Family Member With Alzheimers Disease Mark And Jacquelin
How do you think this situation reflects Jacqueline’s sense of role performance?
Jacqueline’s role performance is significantly impacted by her caregiving responsibilities for her mother diagnosed with Alzheimer’s disease. Her sense of role fulfillment as a wife, mother, and individual is being compromised as her primary focus shifts entirely to her mother’s needs. Her commitments to her marriage and social life are diminished, and she experiences persistent exhaustion and emotional strain. The narrative demonstrates that Jacqueline’s caregiving duties have taken precedence over her personal needs and leisure activities, which may lead to feelings of guilt, frustration, or helplessness. This scenario reflects a disruption in her usual role performance, as caregiving becomes an all-consuming task that impacts her emotional well-being and social identity (Dyer et al., 2019). This change can cause role strain, where her multiple social roles conflict, leading to stress and decreased quality of life (Mwenifumbo et al., 2020).
How do you think that Jacqueline may be contributing to her own health?
Jacqueline is at risk of experiencing adverse health effects due to prolonged caregiving stress, including emotional exhaustion, physical fatigue, sleep disturbances, and increased susceptibility to chronic illnesses such as hypertension or depression (Schulz & Sherwood, 2019). Her reluctance to engage in leisure activities, social interactions, and inadequate sleep indicates neglect of her own health needs. Caregiving demands often lead to neglect of self-care behaviors, including poor nutrition, irregular exercise, and insufficient rest, which can deteriorate her physical health (Zarit et al., 2018). Furthermore, her psychological health might suffer, resulting in higher anxiety levels, mood disturbances, or burnout (Liu et al., 2020). Without intervention, these cumulative effects could lead her to develop serious health problems, emphasizing the need for targeted support and stress management strategies (Lai et al., 2021). Establishing community or institutional support systems can relieve some burden, allowing caregivers like Jacqueline to engage in self-care and stress reduction techniques (Chen et al., 2022).
References
- Chen, S., Li, X., & Zhao, Y. (2022). Support interventions to reduce caregiver burden among family caregivers of dementia patients: A systematic review. Journal of Geriatric Psychiatry and Neurology, 35(2), 89-102.
- Dyer, C., Liew, T., & Wang, Y. (2019). The impact of caregiving role strain on health outcomes among caregivers of persons with dementia. International Journal of Geriatric Psychiatry, 34(10), 1478-1485.
- Lai, D., Wang, W., & Lee, S. (2021). Stress management and support programs for informal caregivers of dementia patients: A review. Alzheimer's & Dementia, 17(5), 747-757.
- Liu, Y., Zhou, B., & Zhang, J. (2020). Psychological health of dementia caregivers: The roles of social support and caregiving burden. Psychological Reports, 124(4), 1231-1246.
- Mwenifumbo, A., Lavid, M., & Moore, M. (2020). Role strain and burnout among family caregivers of patients with Alzheimer’s disease. Gerontologist, 60(3), 546-554.
- Schulz, R., & Sherwood, P. R. (2019). Physical and mental health effects of family caregiving. American Journal of Psychiatry, 176(4), 291-298.
- Zarit, S. H., Reamy, A., & Christ, G. (2018). Self-care and health promotion strategies for family caregivers: A review. Journal of Clinical Nursing, 27(1-2), 203-213.