Abstract
ABSTRACT This paper expands the scope of inquiry into HIV and aging through an ethnographic exploration of a small group of older, long-term (20 or more years) HIV+ gay white men in Toronto who meet fortnightly to discuss and reflect on everyday challenges of living with HIV but do not want to be affiliated with existing HIV/AIDS support organizations. Their discussions reveal a critique of professionalization and biomedical bias in contemporary mainstream Canadian HIV/AIDS discourses and support services, reflecting their shared experiences and memories of the HIV/AIDS epidemic in Canada over many decades. I argue that their frustration with and disengagement from contemporary mainstream HIV/AIDS discourses and support services, based on shared experiences and memories, produces a particular form of “queer viral time,” developed through the intersectional dynamics of epidemiological time, gender, age, race and sexual orientation. Queer viral time draws attention to the temporal dimensions of socio-sexual subject formations, social inequalities, and health governance.
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