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dc.contributor.authorCharles, Gloria A.en_US
dc.date.accessioned2009-05-21T13:25:09Z
dc.date.available2009-05-21T13:25:09Z
dc.date.issued2002-05-21T13:25:09Z
dc.identifier.urihttp://hdl.handle.net/10464/1263
dc.description.abstractThis research is qualitative in nature and has explored, by means of interviews, the '^^ experiences of 10 men in their roles in caring for their spouses with Alzheimer Disease (see glossary) in their homes. Additional data were collected by attending 3 formal support group meetings and one informal meeting of a group of men who brought their wives to a support group meeting for their wives with AD. The data retrieved supported the assumption that education about the disease, utilization of formal community support services, and attendance at caregiver support groups or programs can assist healthy male caregivers in caring for their wives with AD in their homes.en_US
dc.language.isoengen_US
dc.publisherBrock Universityen_US
dc.subjectMale caregivers.en_US
dc.subjectMale caregiversen_US
dc.subjectAlzheimer's diseaseen_US
dc.titleExploring the experiences of male spousal caregivers for their wives with alzheimer disease in their homes : the lived experience and the men's perception of support groups /en_US
dc.typeElectronic Thesis or Dissertationen_US
dc.degree.nameMaster of Educationen_US
dc.degree.levelMastersen_US
dc.contributor.departmentDepartment of Graduate and Undergraduate Studies in Educationen_US
dc.degree.disciplineFaculty of Educationen_US
refterms.dateFOA2021-07-30T02:03:47Z


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