‘It's their blood not mine’

Who’s responsible for (not) telling relatives about genetic risk?

Karen Forrest-Keenan, Sheila A Simpson, Brenda Wilson , Edwin Van Teijlingen, Lorna McKee, Neva E Haites, E Matthews

Research output: Contribution to journalArticle

32 Citations (Scopus)

Abstract

With advances in the 'new genetics', an increasing number of people will have access to genetic information and predictive or susceptibility testing. Genetic knowledge has implications for individuals themselves, as well as other family members. In general, health professionals encourage people to pass on genetic risk information to their relatives. However, the disclosure of such information is not always straightforward and, consequently, some people may not be aware of their risk. If risk information is actively withheld, genetic counsellors may need to determine whether they have a duty to pass this on, particularly when preventive action can be taken. To date, little research has explored the barriers and facilitators in family communication about genetic risk. This paper draws on empirical data from a qualitative study exploring communication in families with late-onset familial disease. Interviews were conducted with participants who received genetic counselling for risk of Huntington's disease and hereditary breast or ovarian cancer. Participants' experiences of who was responsible for (not) telling relatives in their families is studied. A number of themes were identified. These were: (1) 'whose place is it to tell', (2) the gendering of disclosure, and (3) who is 'family'. The implications of these findings are considered.
Original languageEnglish
Pages (from-to)209-226
Number of pages18
JournalHealth, Risk & Society
Volume7
Issue number3
DOIs
Publication statusPublished - Sep 2005

Keywords

  • family communication
  • late-onset genetic risk
  • Huntington's Disease
  • hereditary breast and/or ovarian cancer
  • qualitative study
  • cystic-fibrosis
  • South-Wales
  • cancer-risk
  • information
  • disclosure
  • experience
  • attitudes
  • breast

Cite this

‘It's their blood not mine’ : Who’s responsible for (not) telling relatives about genetic risk? / Forrest-Keenan, Karen; Simpson, Sheila A; Wilson , Brenda; Van Teijlingen, Edwin; McKee, Lorna; Haites, Neva E; Matthews, E.

In: Health, Risk & Society, Vol. 7, No. 3, 09.2005, p. 209-226.

Research output: Contribution to journalArticle

Forrest-Keenan, K, Simpson, SA, Wilson , B, Van Teijlingen, E, McKee, L, Haites, NE & Matthews, E 2005, '‘It's their blood not mine’: Who’s responsible for (not) telling relatives about genetic risk?', Health, Risk & Society, vol. 7, no. 3, pp. 209-226. https://doi.org/10.1080/13698570500229606
Forrest-Keenan, Karen ; Simpson, Sheila A ; Wilson , Brenda ; Van Teijlingen, Edwin ; McKee, Lorna ; Haites, Neva E ; Matthews, E. / ‘It's their blood not mine’ : Who’s responsible for (not) telling relatives about genetic risk?. In: Health, Risk & Society. 2005 ; Vol. 7, No. 3. pp. 209-226.
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