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Understandings of Down's syndrome: A Q methodological investigation

Author

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  • Bryant, Louise D.
  • Green, Josephine M.
  • Hewison, Jenny

Abstract

Down's syndrome has been, and continues to be, a central focus of prenatal testing technology. However, there has been surprisingly little examination of how parental understandings of the condition relate to prenatal testing choices. This study, carried out at the University of Leeds, uses Q methodology to identify 'competing equivalent stories' of Down's syndrome and to highlight the shared and distinct themes within these stories. Seventy-six people were selected as being likely to represent a diverse range of views about Down's syndrome, approximately half of whom had some known experience or expertise related either to the condition or to prenatal testing. The participants were asked to Q sort 50 propositions about Down's syndrome that were selected to reflect different views about the condition in terms of its impact on the affected person, on families with an affected child, and on society. Using Principal Components Analysis, five statistically independent factors were extracted that reflected a range of views towards, and experiences of, people with Down's syndrome. Despite a virtual consensus about the rights of existing people with Down's syndrome to healthcare, an education, and inclusion in their community, there were significant differences in how participants believed they personally would adjust to an affected child. Furthermore, whether or not people with Down's syndrome were seen to be within 'a continuum of normality' sheds light on how views about the condition may be linked to views about prenatal testing and termination of pregnancy. The study demonstrates that people hold complex and sometimes seemingly contradictory views about Down's syndrome, and that these are likely to influence their prenatal testing decisions. Antenatal settings currently provide little opportunity for people to discuss and explore their beliefs about disability. It is argued that this may affect the ability of some individuals to make decisions that are informed by their own views and values.

Suggested Citation

  • Bryant, Louise D. & Green, Josephine M. & Hewison, Jenny, 2006. "Understandings of Down's syndrome: A Q methodological investigation," Social Science & Medicine, Elsevier, vol. 63(5), pages 1188-1200, September.
  • Handle: RePEc:eee:socmed:v:63:y:2006:i:5:p:1188-1200
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    References listed on IDEAS

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    1. Raz, Aviad, 2004. ""Important to test, important to support": attitudes toward disability rights and prenatal diagnosis among leaders of support groups for genetic disorders in Israel," Social Science & Medicine, Elsevier, vol. 59(9), pages 1857-1866, November.
    2. Eccleston, Chris & De C. Williams, Amanda C. & Rogers, Wendy Stainton, 1997. "Patients' and professionals' understandings of the causes of chronic pain: Blame, responsibility and identity protection," Social Science & Medicine, Elsevier, vol. 45(5), pages 699-709, September.
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    1. Gottfre[eth]sdóttir, Helga & Björnsdóttir, Kristín & Sandall, Jane, 2009. "How do prospective parents who decline prenatal screening account for their decision? A qualitative study," Social Science & Medicine, Elsevier, vol. 69(2), pages 274-277, July.
    2. Bryant, Louise D. & Ahmed, Shenaz & Ahmed, Mushtaq & Jafri, Hussain & Raashid, Yasmin, 2011. "'All is done by Allah'. Understandings of Down syndrome and prenatal testing in Pakistan," Social Science & Medicine, Elsevier, vol. 72(8), pages 1393-1399, April.
    3. Ahmed, Shenaz & Bryant, Louise D. & Tizro, Zahra & Shickle, Darren, 2012. "Interpretations of informed choice in antenatal screening: A cross-cultural, Q-methodology study," Social Science & Medicine, Elsevier, vol. 74(7), pages 997-1004.

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