Search
Skip to Search Results- 3Duggleby, W.
- 3Maxwell, Colleen J.
- 3Strain, Laurel A.
- 3Wanless, Deanna
- 2ACCES Research Group
- 2Gilbart, Erin
- 11Graduate and Postdoctoral Studies (GPS), Faculty of
- 11Graduate and Postdoctoral Studies (GPS), Faculty of/Theses and Dissertations
- 9Nursing, Faculty of
- 7Nursing, Faculty of/Chronicity
- 5ACCES Research Group
- 5ACCES Research Group/Research Reports (ACCES)
-
Family members providing home-based palliative care to older adults: The enactment of multiple roles
Download2008
Clemmer, S., Ward-Griffin, C., Forbes, D.
Canadians are experiencing increased life expectancy and chronic illness requiring end-of-life care. There is limited research on the multiple roles for family members providing home-based palliative care. Based on a larger ethnographic study of client-family-provider relationships in home-based...
-
Fall 2016
Approximately 15 million people worldwide experience stroke annually, of which five million are left permanently disabled, creating a need for long term support from family and community services. This sudden, unplanned and unpredictable event can have a devastating effect on the mental and...
-
Hope and connection: The experience of family caregivers of persons with dementia living in a long term care facility.
Download2013
Duggleby, W., Schroeder, D., Nekolaichuk, C.
Background: Hope is a psychosocial resource that is essential for the psychological, spiritual, and physical well-being of family members caring for persons with dementia. A significant positive relationship has been found between hope and well-being in family caregivers of persons with dementia...
-
2013-01-01
Walls-Ingram, Sheena, O'Connell, Megan E., Cammer, Allison, Dal Bello-Haas, Vanina, Stewart, Norma, Crossley, Margaret, Innes, Anthea, Forbes, Dorothy, Morgan, Debra, Kirk, Andrew
Abstract Although only 20-50% of individuals with dementia are diagnosed, early diagnosis enables patients and families to access interventions and services, and plan for the future. The current study explored the experiences of rural family caregivers in the period leading up to a diagnostic...
-
2009
Molzahn, A. E., McNulty, V., Gallagher, E.
The purpose of this study was to describe the quality of life (QOL) of current adult day center (ADC) clients and their family caregivers in one region of Canada. Semi-structured interviews were conducted with 10 ADC clients and 10 caregivers. Data analysis used a modified constant comparative...
-
Role of Caregiver Beliefs About Alzheimer Disease in the Social Creation of Dependency Among Persons With Alzheimer Disease
DownloadFall 2012
It is estimated that over 1.1 million people in Canada will have dementia by 2038 (Alzheimer Society of Canada, 2010). In the caregiving context it is important that independence be maintained for as long as possible. Previous research has shown that caregivers can inadvertently create excess...