Literature DB >> 20065304

Subjective experience of family stigma as reported by children of Alzheimer's disease patients.

Perla Werner1, Dovrat Goldstein, Eli Buchbinder.   

Abstract

In this study we explored the subjective experience of family stigma as reported by children of persons with Alzheimer's disease (AD). Our data indicated that family stigma in the area of AD was primarily experienced in three dimensions: caregivers' stigma, lay public's stigma, and structural stigma. We found that in all these dimensions family stigma follows a process characterized by three core elements: cognitive attributions, emotional reactions, and behavioral responses. Findings of this study highlight the profound stigma confronting caregivers of persons with AD. What emerges is a poignant picture of adult children living with stigmatic beliefs while providing care for their parents with AD. We suggest that swift steps be taken to deal with these stigmatic beliefs. Mainly, structural discrimination must end if all citizens are to receive truly fair and equitable health care services and benefits.

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Year:  2010        PMID: 20065304     DOI: 10.1177/1049732309358330

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


  17 in total

1.  Perceived Challenges in Dementia Care by Vietnamese Family Caregivers and Care Workers in South Australia.

Authors:  Lily Dongxia Xiao; Lesley Habel; Anita De Bellis
Journal:  J Cross Cult Gerontol       Date:  2015-09

2.  The relative contributions of biomarkers, disease modifying treatment, and dementia severity to Alzheimer's stigma: A vignette-based experiment.

Authors:  Shana D Stites; Jeanine Gill; Emily A Largent; Kristin Harkins; Pamela Sankar; Abba Krieger; Jason Karlawish
Journal:  Soc Sci Med       Date:  2021-12-01       Impact factor: 4.634

3.  What features of stigma do the public most commonly attribute to Alzheimer's disease dementia? Results of a survey of the U.S. general public.

Authors:  Shana D Stites; Jonathan D Rubright; Jason Karlawish
Journal:  Alzheimers Dement       Date:  2018-03-27       Impact factor: 21.566

4.  Compassion fatigue: an application of the concept to informal caregivers of family members with dementia.

Authors:  Jennifer R Day; Ruth A Anderson
Journal:  Nurs Res Pract       Date:  2011-09-08

Review 5.  Timely Diagnosis for Alzheimer's Disease: A Literature Review on Benefits and Challenges.

Authors:  Bruno Dubois; Alessandro Padovani; Philip Scheltens; Andrea Rossi; Grazia Dell'Agnello
Journal:  J Alzheimers Dis       Date:  2016       Impact factor: 4.472

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.  From "What the Hell Is Going on?" to the "Mushy Middle Ground" to "Getting Used to a New Normal": Young People's Biographical Narratives Around Navigating Parental Dementia.

Authors:  Mel Hall; Pat Sikes
Journal:  Illn Crises Loss       Date:  2016-05-26

8.  Family members' perspectives on learning cognitively unimpaired older adults' amyloid-β PET scan results.

Authors:  Emily A Largent; Maramawit Abera; Kristin Harkins; Sara J Feldman; Wendy R Uhlmann; J Scott Roberts; Jason Karlawish
Journal:  J Am Geriatr Soc       Date:  2021-07-12       Impact factor: 5.562

9.  Caregiver Stigma and Burden in Memory Disorders: An Evaluation of the Effects of Caregiver Type and Gender.

Authors:  Phoebe V Kahn; Heather A Wishart; Jennifer S Randolph; Robert B Santulli
Journal:  Curr Gerontol Geriatr Res       Date:  2016-01-28

10.  "It was then that I thought 'whaat? This is not my Dad": The implications of the 'still the same person' narrative for children and young people who have a parent with dementia.

Authors:  Pat Sikes; Mel Hall
Journal:  Dementia (London)       Date:  2016-03-07
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