The experience of caring for a family member with Alzheimer's disease.
about
Psychosocial factors that shape patient and carer experiences of dementia diagnosis and treatment: a systematic review of qualitative studiesAnticipatory grief in new family caregivers of persons with mild cognitive impairment and dementia.Health care experiences of people with dementia and their caregivers: a meta-ethnographic analysis of qualitative studiesCaregiver burden and coping strategies in caregivers of patients with Alzheimer's disease.Crisis in access to care: geriatric psychiatry services unobtainable at any price.Negotiating the joint career: couples adapting to Alzheimer's and aging in place.History, development, and future of the progressively lowered stress threshold: a conceptual model for dementia care.Caring for parents with neurodegenerative disease: a qualitative description.Familial caregivers of older adults.Using meta-ethnography to understand the emotional impact of caring for people with increasing cognitive impairment.A recipe for mealtime resilience for families living with dementia.The legitimacy of rest: conditions for the relief of burden in advanced dementia care-giving.Caregiver burden of Mexican dementia patients: the role of dysexecutive syndrome, sleep disorders, schooling and caregiver depression.Sense of coherence, burden, and affective symptoms in family carers of people with dementia.Life orientation in Finnish family caregivers' of persons with Alzheimer's disease: a diary study.Why do patients and their families not use services for dementia? Perspectives from a developed Asian country.Lived experiences of Iranian family member caregivers of persons with Alzheimer's disease: caring as 'captured in the whirlpool of time'.Renewing everyday hope: the hope experience of family caregivers of persons with dementia.Quality of life for caregivers of people with Alzheimer's disease.Socioecological factors and positive aspects of caregiving: findings from the REACH II intervention.Place of death and end-of-life transitions experienced by very old people with differing cognitive status: retrospective analysis of a prospective population-based cohort aged 85 and over.Assessing mental well-being in family carers of people with dementia using the Warwick-Edinburgh Mental Well-Being Scale.Pre-death grief in the context of dementia caregiving: a concept analysis.Stigma among Iranian family caregivers of patients with Alzheimer's disease: A hermeneutic study.Predictors and Moderators of Quality of Life in Alzheimer's Disease Patients.Resourcefulness in African American and Caucasian American Caregivers of Persons With Dementia: Associations With Perceived Burden, Depression, Anxiety, Positive Cognitions, and Psychological Well-Being.Effects of positive cognitions and resourcefulness on caregiver burden among caregivers of persons with dementia.A caregiver perspective of how Alzheimer's disease and related disorders affect couple intimacy.
P2860
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P2860
The experience of caring for a family member with Alzheimer's disease.
description
2001 nî lūn-bûn
@nan
2001年の論文
@ja
2001年学术文章
@wuu
2001年学术文章
@zh
2001年学术文章
@zh-cn
2001年学术文章
@zh-hans
2001年学术文章
@zh-my
2001年学术文章
@zh-sg
2001年學術文章
@yue
2001年學術文章
@zh-hant
name
The experience of caring for a family member with Alzheimer's disease.
@en
The experience of caring for a family member with Alzheimer's disease.
@nl
type
label
The experience of caring for a family member with Alzheimer's disease.
@en
The experience of caring for a family member with Alzheimer's disease.
@nl
prefLabel
The experience of caring for a family member with Alzheimer's disease.
@en
The experience of caring for a family member with Alzheimer's disease.
@nl
P2093
P2860
P1476
The experience of caring for a family member with Alzheimer's disease.
@en
P2093
H K Butcher
K C Buckwalter
P A Holkup
P2860
P356
10.1177/019394590102300104
P577
2001-02-01T00:00:00Z