Literature DB >> 19940091

Managing identity while living with Alzheimer's disease.

Hazel Macrae1.   

Abstract

Although any illness can negatively affect the self, Alzheimer's disease poses a special threat. Based on interviews with nine Canadians diagnosed with early-stage Alzheimer's disease, and adopting a symbolic interactionist perspective, this study examines the impact of the illness on identity. Findings indicate that, given the necessary resources, persons with Alzheimer's can live meaningful, purposeful lives and creatively manage to protect and preserve identity. In contrast to previous research, participants did not reveal a great deal of concern about potential loss of self.

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Year:  2009        PMID: 19940091     DOI: 10.1177/1049732309354280

Source DB:  PubMed          Journal:  Qual Health Res        ISSN: 1049-7323


  12 in total

1.  'The problem here is that they want to solve everything with pills': medication use and identity among Mainland Puerto Ricans.

Authors:  Wallis E Adams; Irina L G Todorova; Mariana T Guzzardo; Luis M Falcón
Journal:  Sociol Health Illn       Date:  2015-02-27

2.  Patient and caregiver goals for dementia care.

Authors:  Lee A Jennings; Alina Palimaru; Maria G Corona; Xavier E Cagigas; Karina D Ramirez; Tracy Zhao; Ron D Hays; Neil S Wenger; David B Reuben
Journal:  Qual Life Res       Date:  2016-12-20       Impact factor: 4.147

3.  Expectations and Concerns of Older Adults With Cognitive Impairment About Their Relationship With Medical Providers: A Call for Therapeutic Alliances.

Authors:  Elena Portacolone; Kenneth E Covinsky; Julene K Johnson; Jodi Halpern
Journal:  Qual Health Res       Date:  2020-06-20

4.  Constructing Couples' Stories: Narrative Practice Insights from a Dyadic Dementia Intervention.

Authors:  Kristin S Scherrer; Berit Ingersoll-Dayton; Beth Spencer
Journal:  Clin Soc Work J       Date:  2014-03-01

5.  Are Humor Styles of People With Dementia Linked to Greater Purpose in Life?

Authors:  Wingyun Mak; Silvia Sörensen
Journal:  Gerontologist       Date:  2018-09-14

6.  Carer Experience Supporting Someone With Dementia and Cancer: A Narrative Approach.

Authors:  Gary Witham; Carol Haigh; Duncan Mitchell; Anna Beddow
Journal:  Qual Health Res       Date:  2017-10-28

7.  Facilitators and barriers to co-research by people with dementia and academic researchers: Findings from a qualitative study.

Authors:  Jacob Waite; Fiona Poland; Georgina Charlesworth
Journal:  Health Expect       Date:  2019-04-22       Impact factor: 3.377

8.  What outcomes are important to patients with mild cognitive impairment or Alzheimer's disease, their caregivers, and health-care professionals? A systematic review.

Authors:  Claire Tochel; Michael Smith; Helen Baldwin; Anders Gustavsson; Amanda Ly; Christin Bexelius; Mia Nelson; Christophe Bintener; Enrico Fantoni; Josep Garre-Olmo; Olin Janssen; Christoph Jindra; Isabella F Jørgensen; Alex McKeown; Buket Öztürk; Anna Ponjoan; Michele H Potashman; Catherine Reed; Emilse Roncancio-Diaz; Stephanie Vos; Cathie Sudlow
Journal:  Alzheimers Dement (Amst)       Date:  2019-03-07

Review 9.  Psychosocial factors that shape patient and carer experiences of dementia diagnosis and treatment: a systematic review of qualitative studies.

Authors:  Frances Bunn; Claire Goodman; Katie Sworn; Greta Rait; Carol Brayne; Louise Robinson; Elaine McNeilly; Steve Iliffe
Journal:  PLoS Med       Date:  2012-10-30       Impact factor: 11.069

10.  Subjective experiences of cognitive decline and receiving a diagnosis of dementia: qualitative interviews with people recently diagnosed in memory clinics in the UK.

Authors:  Penny Xanthopoulou; Rose McCabe
Journal:  BMJ Open       Date:  2019-08-01       Impact factor: 2.692

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