'the forgotten epidemic': world's largest hiv/aids conference will draw thousands to montreal
"community engagement makes science better and results of uptake better. we learned this from hiv.”
stigma. it’s not something you would expect 40 years into what casey house ceo joanne simons refers to as the hiv pandemic. that 40 years represents decades of scientific advancements and educational outreach, to show the public the truth about living with hiv. but, as members of the casey house community explained at the others premiere on wednesday, misinformation and hostility is still all too common.
individuals living with hiv are twice as likely to have depression, due in large part to the stress associated with living with the diagnosis, according to the national institutes of health . stigma has also been associated with creating barriers to treatment, care and support services and causing patients to develop internalized stigma — both of which can result in higher levels of anxiety, lower quality of life and lower adherence to antiretroviral therapy.
others , a slow-burn short horror film, explores the terror caused by stigma and what it means when someone cannot trust the kind gestures of strangers. healthing sat down with director paul shkordoff to talk about approaching this short movie and how the fear of stigma played a very real role in its development.
this interview has been edited for length and clarity.
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how did you first get involved with the movie?
you mentioned it took about a year from concept to final film — what was the development process like?
once we found peter [ mcpherson] , we wanted to adjust the story. we completely threw out the old script because we wanted to craft a story that felt closer to — not necessarily peter’s experience — but who peter was as a person. [a story] that didn’t feel like we were asking him to reach outside of his comfort zone in terms of the character he was trying to portray. we really tried to create a space where he could bring as much of his own experience to the film.
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how did you approach fleshing out a story on the stigma people living with hiv have experienced, while still being respectful?
i had the opportunity to go to casey house early in 2022. covid-19 was still on the horizon. i think an omicron wave had just passed and they had set up — as safe as they possibly could — the opportunity for me to speak with clients of theirs who were staying at casey house. and we just had a conversation. i was telling them about the film and asking them, does it feel truthful? does that feel real? but also, just letting them speak and trying to reflect back the many experiences that i had the opportunity to learn from and hear about through casey house.
one of the goals for this film was to have a lead protagonist who lives with hiv. how did you go about that?
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we reached out to casting agents that opc had a relationship with. we casted in canada, across the country. but then we started to reach out to casting agents in the u.s. and all the big markets in new york and l.a., and europe as well. it was just proving how necessary the film was, because there was a stigma that we were constantly coming up against from casting agencies. [we were told] no one wants to come out for this role, because they don’t want people to know that they are living with hiv. they didn’t want to carry that stigma with them as a result of taking the role. it was so eye opening; it really just proved how necessary the film was.
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emma jones is a multimedia editor with healthing. you can reach her at emjones@postmedia.com or on instagram and twitter @jonesyjourn .