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The disclosure of one’s HIV-positive status is a personal decision that can play an
important role in engagement in HIV treatment and care. Social network approaches
situate individuals within broader webs of social connections that influence health
and wellbeing and thus hold the potential to elucidate key social factors shaping the
process of disclosure. As part of a larger clinical study examining how substance use
and mental health shape HIV outcomes, we recruited 61 individuals newly diagnosed
with HIV at two clinics in Western Kenya to participate in an egocentric social net-
works study. We conducted a survey that generated a visual network map to guide
a subsequent qualitative interview about experiences being diagnosed and living
with HIV. We thematically analyzed the qualitative data and visual network maps to
examine the social contexts and patterns of HIV disclosure, with the goal of identify-
ing supportive contexts of disclosure. The mean age was 36.7 years (range: 20–62);
women were significantly younger than men and more likely to self-report a mental
health issue. Typically, participants disclosed their HIV-positive status to a small num-
ber of close, trusted alters in their network, including intimate partners, siblings and
other family members, and friends. The need for mental health support in the wake of
a new diagnosis, especially among women, encouraged disclosure. Across nearly all
stories, stigma was a powerful deterrent to sharing one’s status, and multiple people
noted prior disclosure to others not named in their current networks because their
relationships were negatively impacted. Our study shows how the intersection of
social relationships, mental health, and stigma is critical in understanding
decision-making processes around disclosure. Selective disclosure typically improved participants’ wellbeing while stigma precluded disclosure and exacerbated distress.
Our study offers suggestions for social network interventions to support people living
with HIV/AIDS. |
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