Vis enkel innførsel

dc.contributor.authorSolbrække, Kari Nyheim
dc.contributor.authorSøiland, Håvard
dc.contributor.authorLode, Kirsten
dc.contributor.authorGripsrud, Birgitta Haga
dc.date.accessioned2018-02-07T09:01:13Z
dc.date.available2018-02-07T09:01:13Z
dc.date.created2016-09-13T08:52:18Z
dc.date.issued2017-03
dc.identifier.citationSolbrække, K. N. et al. (2017) Our genes, our selves: hereditary breast cancer and biological citizenship in Norway. Medicine, Health care and Philosophy. 20(1), pp. 89-103.nb_NO
dc.identifier.issn1386-7423
dc.identifier.urihttp://hdl.handle.net/11250/2483158
dc.descriptionThis is a post-peer-review, pre-copyedit version of an article published in "Medicine, Health Care and Philosophy". The final authenticated version is available online at: http://dx.doi.org/10.1007/s11019-016-9737-y.nb_NO
dc.description.abstractIn this paper we explore the rise of ‘the breast cancer gene’ as a field of medical, cultural and personal knowledge. We address its significance in the Norwegian public health care system in relation to so-called biological citizenship in this particular national context. One of our main findings is that, despite its claims as a measure for health and disease prevention, gaining access to medical knowledge of BRCA 1/2 breast cancer gene mutations can also produce severe instability in the individuals and families affected. That is, although gene testing provides modern subjects with an opportunity to foresee their biological destiny and thereby become patients in waiting, it undoubtedly also comes with difficult existential dilemmas and choices, with implications that resonate beyond the individual and into different family and love relations. By elaborating on this finding we address the question of whether the empowerment slogan, which continues to be advocated through various health, BRCA and breast cancer discourses, reinforces a naïve or an idealized notion of the actively responsible patient: resourceful enough to seek out medical expertise and gain sufficient knowledge, on which to base informed decisions, thereby reducing the future risk of developing disease. In contrast to this ideal, our Norwegian informants tell a different story, in which there is no apparent heroic mastery of genetic fates, but rather a pragmatic attitude to dealing with a dire situation over which they have little control, despite having complied with medical advice through national guidelines and follow-up procedures for BRCA 1/2 carriers. In conclusion we claim that the sense of safety that gene testing and its associated medical solutions allegedly promise to provide proved illusory. Although BRCA-testing offers the potential for protection from adverse DNA-heritage, administered through possibilities for self-monitoring and self-management of the body, the feeling of ‘being in good health’ has hardly been reinforced by the emergence of gene technology.nb_NO
dc.language.isoengnb_NO
dc.publisherSpringer Netherlandsnb_NO
dc.subjectbrystkreftnb_NO
dc.subjectarvelig brystkreftnb_NO
dc.subjectgenernb_NO
dc.subjectgentestingnb_NO
dc.subjectbiological citizenshipnb_NO
dc.subjectsubjectivitynb_NO
dc.subjectbreast cancernb_NO
dc.titleOur genes, our selves: hereditary breast cancer and biological citizenship in Norwaynb_NO
dc.typeJournal articlenb_NO
dc.typePeer reviewednb_NO
dc.description.versionacceptedVersionnb_NO
dc.rights.holder© Springer Science+Business Media Dordrecht 2016nb_NO
dc.subject.nsiVDP::Medical disciplines: 700::Clinical medical disciplines: 750::Oncology: 762nb_NO
dc.source.pagenumber89-103nb_NO
dc.source.volume20nb_NO
dc.source.journalMedicine, Health care and Philosophynb_NO
dc.source.issue1nb_NO
dc.identifier.doi10.1007/s11019-016-9737-y
dc.identifier.cristin1380621
dc.relation.projectUniversitetet i Stavanger: IN-10208nb_NO
cristin.unitcode217,13,0,0
cristin.unitnameDet helsevitenskapelige fakultet
cristin.ispublishedtrue
cristin.fulltextpostprint
cristin.qualitycode1


Tilhørende fil(er)

Thumbnail

Denne innførselen finnes i følgende samling(er)

Vis enkel innførsel