Literature DB >> 24602967

The expressivist objection to prenatal testing: the experiences of families living with genetic disease.

Felicity Kate Boardman1.   

Abstract

The expressivist objection to prenatal testing is acknowledged as a significant critique of prenatal testing practices most commonly advanced by disability rights supporters. Such writers argue that prenatal testing and selective termination practices are objectionable as they express disvalue not only of the foetus being tested, but also of disabled people as a whole, by focusing exclusively on the disabling trait. While the objection has been widely critiqued on the basis of its theoretical incoherence, this paper highlights the way in which it, nevertheless, is a significant mediator in decisions around the use of reproductive genetic technologies. By drawing on 41 in-depth qualitative interviews (drawn from a sample of 61) conducted in the UK between 2007 and 2009 with families and individuals living with a genetic disease, Spinal Muscular Atrophy (SMA), this paper highlights the ways in which expressivist objections feature prominently in the reproductive decisions of families living with SMA and the significant emotional burden they represent. While the literature on the expressivist objection has focused on the reproductive decisions of those undergoing prenatal testing for a condition of which they have little (or no) prior knowledge, the context of intimate familial relationships and extensive experience with the tested-for condition fundamentally alters the nature and impact of expressivist objections within families living with an inheritable condition. By focussing on the reproductive decisions of families living with SMA and their strategic management of the expressivist objection, this paper will address the call, made primarily by disability rights supporters, for 'experientially based' (as opposed to medical) information about the tested-for disability to be made available to would-be parents considering selective termination. It will be argued that parents' experiential knowledge of the tested-for disability can, in fact, amplify expressivist objections to prenatal testing, and thus paradoxically constrain, rather than facilitate, reproductive decisions.
Copyright © 2014 The Author. Published by Elsevier Ltd.. All rights reserved.

Entities:  

Keywords:  Disability rights; Expressivist objection; Genetic risk; Qualitative; Reproductive decision making; Spinal Muscular Atrophy; UK

Mesh:

Year:  2014        PMID: 24602967     DOI: 10.1016/j.socscimed.2014.02.025

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


  15 in total

1.  "This lifetime commitment": Public conceptions of disability and noninvasive prenatal genetic screening.

Authors:  Rosemary J Steinbach; Megan Allyse; Marsha Michie; Emily Y Liu; Mildred K Cho
Journal:  Am J Med Genet A       Date:  2015-11-14       Impact factor: 2.802

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

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

3.  It's complicated - Factors predicting decisional conflict in prenatal diagnostic testing.

Authors:  Cécile Muller; Linda D Cameron
Journal:  Health Expect       Date:  2015-04-13       Impact factor: 3.377

4.  Family Sense-Making After a Down Syndrome Diagnosis.

Authors:  Lauren Clark; Heather E Canary; Kyle McDougle; Rebekah Perkins; Ruth Tadesse; Avery E Holton
Journal:  Qual Health Res       Date:  2020-07-03

5.  Using ethnodrama to support parents in sense-making after prenatal or neonatal diagnosis of a child's disabling condition.

Authors:  Jacqueline Eaton; Sydney Cheek-O'Donnell; Erin Johnson; Lauren Clark
Journal:  J Appl Res Intellect Disabil       Date:  2021-10-27

6.  Disability Experiences and Perspectives Regarding Reproductive Decisions, Parenting, and the Utility of Genetic Services: a Qualitative Study.

Authors:  C Roadhouse; C Shuman; K Anstey; K Sappleton; D Chitayat; E Ignagni
Journal:  J Genet Couns       Date:  2018-06-16       Impact factor: 2.537

7.  Spanish- and English-Speaking Pregnant Women's Views on cfDNA and Other Prenatal Screening: Practical and Ethical Reflections.

Authors:  Erin Floyd; Megan A Allyse; Marsha Michie
Journal:  J Genet Couns       Date:  2016-01-07       Impact factor: 2.537

8.  Generating a taxonomy for genetic conditions relevant to reproductive planning.

Authors:  Diane M Korngiebel; Carmit K McMullen; Laura M Amendola; Jonathan S Berg; James V Davis; Marian J Gilmore; Cary O Harding; Patricia Himes; Gail P Jarvik; Tia L Kauffman; Kathleen A Kennedy; Dana Kostiner Simpson; Michael C Leo; Frances L Lynch; Denise I Quigley; Jacob A Reiss; C Sue Richards; Alan F Rope; Jennifer L Schneider; Katrina A B Goddard; Benjamin S Wilfond
Journal:  Am J Med Genet A       Date:  2016-03       Impact factor: 2.802

9.  The role of experiential knowledge within attitudes towards genetic carrier screening: A comparison of people with and without experience of spinal muscular atrophy.

Authors:  Felicity K Boardman; Philip J Young; Oliver Warren; Frances E Griffiths
Journal:  Health Expect       Date:  2017-07-13       Impact factor: 3.377

10.  Anticipated stigma and blameless guilt: Mothers' evaluation of life with the sex-linked disorder, hypohidrotic ectodermal dysplasia (XHED).

Authors:  Angus Clarke
Journal:  Soc Sci Med       Date:  2016-04-25       Impact factor: 4.634

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