The Cancer’s Margins Project: Access to Knowledge and Its Mobilization by LGBQ/T Cancer Patients

Detalhes bibliográficos
Autor(a) principal: Taylor, Evan T.
Data de Publicação: 2019
Outros Autores: Bryson, Mary K., Boschman, Lorna, Hart, Tae, Gahagan, Jacqueline, Rail, Genevieve, Ristock, Janice
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Texto Completo: https://doi.org/10.17645/mac.v7i1.1718
Resumo: Sexual and/or gender minority populations (LGBQ/T) have particular cancer risks, lower involvement in cancer screening, and experience barriers in communication with healthcare providers. All of these factors increase the probability of health decisions linked with poor outcomes that include higher levels of cancer mortality. Persistent discrimination against, and stigmatization of, LGBQ/T people is reflected in sparse medical curriculum addressing LGBQ/T communities. Marginalization makes LGBQ/T persons particularly reliant on knowledge derived from online networks and mainstream media sources. In what is likely the first nationally-funded and nation-wide study of LGBQ/T experiences of cancer, the Cancer’s Margins project (www.lgbtcancer.ca) conducted face-to-face interviews with 81 sexual and/or gender minority patients diagnosed and treated for breast and/or gynecological cancer in five Canadian provinces and the San Francisco Bay area (US). With specific attention to knowledge access, sharing, and mobilization, our objective was to document and analyze complex intersectional relationships between marginalization, gender and sexuality, and cancer health decision-making and care experiences. Findings indicate that cancer care knowledge in online environments is shaped by cisnormative and heteronormative narratives. Cancer knowledge and support environments need, by contrast, to be designed by taking into account intersectionally diverse models of minority identities and communities.
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spelling The Cancer’s Margins Project: Access to Knowledge and Its Mobilization by LGBQ/T Cancer Patientsbiographical knowledge; biomedical knowledge; cancer; cancer care; gender; health disparities; health equity; information access; LGBT health; minority cancer patients; transgender; treatmentSexual and/or gender minority populations (LGBQ/T) have particular cancer risks, lower involvement in cancer screening, and experience barriers in communication with healthcare providers. All of these factors increase the probability of health decisions linked with poor outcomes that include higher levels of cancer mortality. Persistent discrimination against, and stigmatization of, LGBQ/T people is reflected in sparse medical curriculum addressing LGBQ/T communities. Marginalization makes LGBQ/T persons particularly reliant on knowledge derived from online networks and mainstream media sources. In what is likely the first nationally-funded and nation-wide study of LGBQ/T experiences of cancer, the Cancer’s Margins project (www.lgbtcancer.ca) conducted face-to-face interviews with 81 sexual and/or gender minority patients diagnosed and treated for breast and/or gynecological cancer in five Canadian provinces and the San Francisco Bay area (US). With specific attention to knowledge access, sharing, and mobilization, our objective was to document and analyze complex intersectional relationships between marginalization, gender and sexuality, and cancer health decision-making and care experiences. Findings indicate that cancer care knowledge in online environments is shaped by cisnormative and heteronormative narratives. Cancer knowledge and support environments need, by contrast, to be designed by taking into account intersectionally diverse models of minority identities and communities.Cogitatio2019-02-05info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleapplication/pdfhttps://doi.org/10.17645/mac.v7i1.1718oai:ojs.cogitatiopress.com:article/1718Media and Communication; Vol 7, No 1 (2019): Communicating on/with Minorities; 102-1132183-2439reponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãoinstacron:RCAAPenghttps://www.cogitatiopress.com/mediaandcommunication/article/view/1718https://doi.org/10.17645/mac.v7i1.1718https://www.cogitatiopress.com/mediaandcommunication/article/view/1718/1718https://www.cogitatiopress.com/mediaandcommunication/article/downloadSuppFile/1718/391Copyright (c) 2019 Evan T. Taylor, Mary K. Bryson, Lorna Boschman, Tae Hart, Jacqueline Gahagan, Genevieve Rail, Janice Ristockhttp://creativecommons.org/licenses/by/4.0info:eu-repo/semantics/openAccessTaylor, Evan T.Bryson, Mary K.Boschman, LornaHart, TaeGahagan, JacquelineRail, GenevieveRistock, Janice2022-12-20T10:57:36Zoai:ojs.cogitatiopress.com:article/1718Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-19T16:20:19.046176Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãofalse
dc.title.none.fl_str_mv The Cancer’s Margins Project: Access to Knowledge and Its Mobilization by LGBQ/T Cancer Patients
title The Cancer’s Margins Project: Access to Knowledge and Its Mobilization by LGBQ/T Cancer Patients
spellingShingle The Cancer’s Margins Project: Access to Knowledge and Its Mobilization by LGBQ/T Cancer Patients
Taylor, Evan T.
biographical knowledge; biomedical knowledge; cancer; cancer care; gender; health disparities; health equity; information access; LGBT health; minority cancer patients; transgender; treatment
title_short The Cancer’s Margins Project: Access to Knowledge and Its Mobilization by LGBQ/T Cancer Patients
title_full The Cancer’s Margins Project: Access to Knowledge and Its Mobilization by LGBQ/T Cancer Patients
title_fullStr The Cancer’s Margins Project: Access to Knowledge and Its Mobilization by LGBQ/T Cancer Patients
title_full_unstemmed The Cancer’s Margins Project: Access to Knowledge and Its Mobilization by LGBQ/T Cancer Patients
title_sort The Cancer’s Margins Project: Access to Knowledge and Its Mobilization by LGBQ/T Cancer Patients
author Taylor, Evan T.
author_facet Taylor, Evan T.
Bryson, Mary K.
Boschman, Lorna
Hart, Tae
Gahagan, Jacqueline
Rail, Genevieve
Ristock, Janice
author_role author
author2 Bryson, Mary K.
Boschman, Lorna
Hart, Tae
Gahagan, Jacqueline
Rail, Genevieve
Ristock, Janice
author2_role author
author
author
author
author
author
dc.contributor.author.fl_str_mv Taylor, Evan T.
Bryson, Mary K.
Boschman, Lorna
Hart, Tae
Gahagan, Jacqueline
Rail, Genevieve
Ristock, Janice
dc.subject.por.fl_str_mv biographical knowledge; biomedical knowledge; cancer; cancer care; gender; health disparities; health equity; information access; LGBT health; minority cancer patients; transgender; treatment
topic biographical knowledge; biomedical knowledge; cancer; cancer care; gender; health disparities; health equity; information access; LGBT health; minority cancer patients; transgender; treatment
description Sexual and/or gender minority populations (LGBQ/T) have particular cancer risks, lower involvement in cancer screening, and experience barriers in communication with healthcare providers. All of these factors increase the probability of health decisions linked with poor outcomes that include higher levels of cancer mortality. Persistent discrimination against, and stigmatization of, LGBQ/T people is reflected in sparse medical curriculum addressing LGBQ/T communities. Marginalization makes LGBQ/T persons particularly reliant on knowledge derived from online networks and mainstream media sources. In what is likely the first nationally-funded and nation-wide study of LGBQ/T experiences of cancer, the Cancer’s Margins project (www.lgbtcancer.ca) conducted face-to-face interviews with 81 sexual and/or gender minority patients diagnosed and treated for breast and/or gynecological cancer in five Canadian provinces and the San Francisco Bay area (US). With specific attention to knowledge access, sharing, and mobilization, our objective was to document and analyze complex intersectional relationships between marginalization, gender and sexuality, and cancer health decision-making and care experiences. Findings indicate that cancer care knowledge in online environments is shaped by cisnormative and heteronormative narratives. Cancer knowledge and support environments need, by contrast, to be designed by taking into account intersectionally diverse models of minority identities and communities.
publishDate 2019
dc.date.none.fl_str_mv 2019-02-05
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https://doi.org/10.17645/mac.v7i1.1718
https://www.cogitatiopress.com/mediaandcommunication/article/view/1718/1718
https://www.cogitatiopress.com/mediaandcommunication/article/downloadSuppFile/1718/391
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dc.publisher.none.fl_str_mv Cogitatio
publisher.none.fl_str_mv Cogitatio
dc.source.none.fl_str_mv Media and Communication; Vol 7, No 1 (2019): Communicating on/with Minorities; 102-113
2183-2439
reponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
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