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dc.rights.licensehttps://creativecommons.org/licenses/by/4.0/legalcode
dc.contributor.authorPomeranz, Deborah
dc.date.accessioned2025-06-20T07:21:26Z
dc.date.available2025-06-20T07:21:26Z
dc.date.issued2022
dc.identifier.issnissn:0948-9975
dc.identifier.urihttps://www.genderopen.de/25595/3941
dc.description.abstractThere is a particular impetus to consider the history of the US AIDS epidemic through an intersectional lens, given that the inequities structuring the early years of the crisis continue to be reproduced in the popular imagination of its history. Iris De La Cruz (1953-1991) is often mobilized in this context as an example of the diversity of AIDS activism as well as of the epidemic’s disproportionate toll on marginalized groups. However, this framing, though well-intentioned, positions De La Cruz’s AIDS diagnosis as the entry point to her life and historical significance. Further, by identifying marginalized women with their serostatus, it privileges oversimplified associations over self-identification and historical specificity, emptying the lives of women with AIDS of individuality. Overall, narratives of De La Cruz as an AIDS fighter, activist, and simply as a woman with AIDS disregard the rest of her vibrant life and reveal nothing about her that could not have been said in advance.
dc.language.isoeng
dc.subjectAIDS
dc.subjectFrauengeschichte
dc.subjectHIV/AIDS
dc.subjectIris De La Cruz
dc.subjectRepräsentation
dc.subjectUS-Geschichte
dc.subject.ddcddc:900
dc.titleRepresenting AIDS’ Invisible Subjects: Iris De La Cruz and the Historical Intersectional-Recovery Imperative
dc.typearticle
dc.typearticle
dc.identifier.doihttp://dx.doi.org/10.25595/3935
dc.source.pageinfo73–88
dc.type.versionpublishedVersion
dc.source.journalFZG (FZG – Freiburger Zeitschrift für GeschlechterStudien)
dc.source.issue1
dc.source.volume28
dc.identifier.pihttps://doi.org/10.3224/fzg.v28i1.05
local.typeZeitschriftenartikel


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