Background: Family carers of people living with dementia provide care over many months or years with little to no formal support. Carers' experiences of compassion for themselves and others including receiving compassion can influence their caregiving experience and the quality of care they provide. However, little is known about healthcare professionals (HCPs) understanding of how compassion is experienced by family carers and how best HCPs can support family carers to cultivate and maintain compassion for themselves and others.
Methods: This study used qualitative interviews to explore family carers experience of compassion for themselves and others (including receiving compassion from others) while caring for someone living with dementia. Inductive thematic analysis was used to explore and report the barriers and facilitators to family carers experiences of compassion.
Results: Interviews with ten family carers (nine current and one former carer) comprising of five daughters, three wives, one husband and one son were undertaken. Barriers and facilitators were identified for compassion for self, others and receiving compassion. While facilitators to compassion included having the opportunity to maintain an identify outside of caring role, positive memories, and shared understanding, experiences that made it difficult for carers to maintain compassion included the perception that one needs to sacrifice own needs and feelings of guilt and shame.
Conclusions: Preliminary findings indicate that whilst carers of people living with dementia acknowledge that compassion is important, they indicate that the caring role could be a barrier to experiencing and maintaining compassion. Future research needs to focus on developing supportive interventions designed to addressing factors that may hinders carers abilities to cultivate and maintain compassion.
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http://dx.doi.org/10.1002/alz.088926 | DOI Listing |
Alzheimers Dement
December 2024
The University of Texas Health Science Center at San Antonio, San Antonio, TX, USA.
Background: Approximately 6.7 million people in the US are diagnosed with an Alzheimer's disease (AD), with greater incidence in women and minorities. Approximately 11 million family members provide uncompensated care to their family members with dementia, with more than 60% reporting high or very high levels of stress, a condition associated with increased risk for AD.
View Article and Find Full Text PDFAlzheimers Dement
December 2024
Washington University in St. Louis School of Medicine, St. Louis, MO, USA.
Background: Alzheimer disease (AD) related cognitive decline occurs at relatively young ages in individuals with Down syndrome (DS, early-mid 50s) and in those with autosomal dominant mutations (ADAD, 40-50s). Both groups show similar patterns of amyloid accumulation. We examined if brain volumes are similarly affected by AD pathology in individuals with DS and ADAD.
View Article and Find Full Text PDFAlzheimers Dement
December 2024
Federal University of Sao Paulo (UNIFESP), Sao Paulo, Brazil.
Background: (1) to present the main findings of two National Dementia Reports developed in partnership with the Brazilian Ministry of Health; (2) to summarize and discuss the proposed public health initiatives to respond to the challenges identified in the reports.
Methods: Desk review, bibliometric study, cross sectional data and secondary analysis of existing data.
Results: There is a lack of knowledge in Brazil in most parts of the country about the epidemiology as well as other important dementia-related factors.
Alzheimers Dement
December 2024
Emory University Nell Hodgson Woodruff School of Nursing, Atlanta, GA, USA.
Background: One in five people with cognitive impairment or dementia lacks family caregivers. People aging alone receive care from non-family sources, including friends and neighbors, but the dynamics of these relationships are unexplored.
Method: Thematic analysis of qualitative interviews with 15 people with cognitive impairment or early dementia without close family and 14 non-family caregivers RESULT: We identified five themes that shape non-family dementia caregiving dynamics: 1) establishing a relationship of trust, 2) personal motivations for seeking/providing care, 3) negotiating caregiving etiquette, 4) establishing caregiving boundaries, 5) the role of distant family.
Background: The survival outcomes following an Alzheimer's disease (AD) diagnosis hold significant importance for health management, caregivers, patients, and their families. Hawaii is known as the most diverse ethnic population in the United States and there exist significant racial health disparities. This study investigates racial/ethnic disparities in survival among AD patients in Hawaii and develops Machine Learning models for overall survival prediction, utilizing Hawaii Medicare data.
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