Open AccessCrisis of Erasure
Author(s) -
Curtis S. Tenney,
Karl Surkan,
Lynette Hammond Gerido,
Dawn Betts-Green
Publication year - 2021
Publication title -
the international journal of information, diversity, and inclusion
Language(s) - English
Resource type - Journals
ISSN - 2574-3430
DOI - 10.33137/ijidi.v5i4.37406
Subject(s) - transgender , breast cancer , normative , population , health care , femininity , human sexuality , psychology , social psychology , gender studies , medicine , sociology , cancer , demography , political science , law
In this paper, we use the topic of breast cancer as an example of health crisis erasure in both informational and institutional contexts, particularly within the transgender and gender-nonconforming population. Breast cancer health information conforms and defaults to conventional cultural associations with femininity, as is the case with pregnancy and other “single-sex” conditions (Surkan, 2015). Many health information and research practices normalize sexualities, pathologize non-normative gender (Drescher et al., 2012; Fish, 2008; Müller, 2018), and fail to recognize gender-nonconforming categories (Frohard‐Dourlent et al., 2017). Because breast cancer health information is sexually normalized, an information boundary exists for the LGBTQ+ community, particularly among transgender and gender-nonconforming adults who are at greater risk of discrimination in healthcare settings (Casey et al., 2019). Transgender and gender-nonconforming people experience unique marginalization and risk with respect to breast cancer. We call upon and propose library and information research, education, and practice opportunities inclusive of the health information needs of transgender and gender-nonconforming populations.