Literature DB >> 16431006

The best experts: the narratives of those who have a genetic condition.

Alan Petersen1.   

Abstract

In recent years, there have been growing expectations about the future benefits deriving from the uptake of genetics knowledge in healthcare. At the same time, there have been increasing calls to make greater use of patient expertise in treatment. However, relatively little is known about the experiences, needs and expertise of those who currently have a genetic condition. Drawing on the findings from an Australian study involving 21 semi-structured interviews with members of support groups which represent those with various genetic conditions (cystic fibrosis, haemochromatosis, haemophilia, and thalassaemia) this article discusses how individuals learn about, live with and manage their condition, and assesses the extent to which their experiences differ from those with other chronic illness conditions. It argues that while the experiences of individuals who have a genetic condition would appear to be similar in many respects to those with other chronic illnesses, they tend to encounter particular challenges in managing their condition due to its inheritable nature.

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Mesh:

Year:  2006        PMID: 16431006     DOI: 10.1016/j.socscimed.2005.11.068

Source DB:  PubMed          Journal:  Soc Sci Med        ISSN: 0277-9536            Impact factor:   4.634


  21 in total

1.  Agency and choice in genetic counseling: Acknowledging patients' concerns.

Authors:  Kieran O'Doherty
Journal:  J Genet Couns       Date:  2009-10       Impact factor: 2.537

2.  Grandmothers as gems of genetic wisdom: exploring South African traditional beliefs about the causes of childhood genetic disorders.

Authors:  Claire Penn; Jennifer Watermeyer; Carol MacDonald; Colleen Moabelo
Journal:  J Genet Couns       Date:  2009-09-25       Impact factor: 2.537

Review 3.  The relationship between the genetic counseling profession and the disability community: a commentary.

Authors:  Anne C Madeo; Barbara B Biesecker; Campbell Brasington; Lori H Erby; Kathryn F Peters
Journal:  Am J Med Genet A       Date:  2011-05-12       Impact factor: 2.802

4.  Narrating disability, narrating religious practice: reconciliation and fragile X syndrome.

Authors:  Marsha Michie; Debra Skinner
Journal:  Intellect Dev Disabil       Date:  2010-04

5.  Talking about disability in prenatal genetic counseling: a report of two interactive workshops.

Authors:  Jan Hodgson; Jon Weil
Journal:  J Genet Couns       Date:  2011-10-25       Impact factor: 2.537

6.  Human genome editing and the identity politics of genetic disability.

Authors:  Felicity Boardman
Journal:  J Community Genet       Date:  2019-09-06

7.  Self-management and skills acquisition in boys with haemophilia.

Authors:  Kate Khair; Liz Meerabeau; Faith Gibson
Journal:  Health Expect       Date:  2013-05-27       Impact factor: 3.377

Review 8.  Disclosure of genetic information within families.

Authors:  Agatha M Gallo; Denise B Angst; Kathleen A Knafl
Journal:  Am J Nurs       Date:  2009-04       Impact factor: 2.220

9.  A place for genetic uncertainty: parents valuing an unknown in the meaning of disease.

Authors:  Ian Whitmarsh; Arlene M Davis; Debra Skinner; Donald B Bailey
Journal:  Soc Sci Med       Date:  2007-06-11       Impact factor: 4.634

10.  Presenting life with cystic fibrosis: a Q-methodological approach to developing balanced, experience-based prenatal screening information.

Authors:  Katherine F Wright; Louise D Bryant; Stephen Morley; Jenny Hewison; Alistair J A Duff; Daniel Peckham
Journal:  Health Expect       Date:  2013-08-02       Impact factor: 3.377

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