advertisement

as told to: 'being hiv-positive enabled me to find a real passion and life purpose'

christian hui, a toronto-based hiv+ activist and social worker, shares his story of triumph over racism, xenophobia and homophobia.

as told to: 'being hiv positive enabled me to find a real passion and life purpose'
why haven’t governments around the world come together to bring about an overall solution? everyone in the world who is living with hiv should already have access to medication. getty
christian hui is a toronto-based hiv+ activist and social worker who is dedicated to bringing awareness to hiv stigma and the importance of treatment. he is a cihr vanier graduate scholar and policy studies phd candidate, and is the co-founder of ontario positive asians (opa+) and the canadian positive people network (cppn). he is also a senior global community advisor at prevention access campaign. in the new year, he will begin work as the north american delegate for the ngo delegation to the unaids programme coordinating board (pcb). this is his story.  
i am 43 years old, and i have lived with hiv for 18 years. as a young adult, even though i knew about hiv prevention, just being queer, having been bullied, and experiencing racism, xenophobia and homophobia when i moved to the u.s. as a settler immigrant — all that discrimination impacted me in terms of the choices that i was able to make, for example, how i was negotiating safer sex and connecting with other queer men. so when i was diagnosed, i didn’t take the news well at all. i didn’t see anyone for about six months, and went into a deep depression.

i had internalized the stigma as a queer asian

a friend of mine, who i considered my canadian brother and who passed away a couple of years ago, was active in the community and would link me with services that were fighting the stigma. but the way that i had internalized the stigma as a queer asian, i didn’t want to seek those services. i felt ashamed when i thought about it, i didn’t want to go to the food bank, i didn’t want to see the caseworker, i resisted treatment, all because i was needing to process my diagnosis. and at that time, treatment access was not at its best. to this day, hiv medication is very expensive. then, organizations were recommending people who tested positive to go on disability and i did. my psyche, then, was dealing with the diagnosis, but also with being on social assistance. it was tough because i come from a culture where we’re expected to be professionals — doctors, lawyers, whatever — and i was not any of that. it was a mind-fuck dealing with that and the fear that people might ostracize me. it took me a while to sort through that.
story continues below

advertisement

today, i would say being hiv+ is one of the best things that has happened to me in the sense that it enabled me to find a real passion and life purpose. after trying to cope with the diagnosis through substance use, i was tested for hepatitis c, and was living with both. i asked myself, ‘do i want to live or do i want to die?’ so i went through treatment for my substance use, and i recognized that i wanted to volunteer and start rebuilding my life. i found an agency where i eventually started working for a number of years. it is an ethno-cultural specific organization called acas (asian community aids services). they serve east and southeast asians living with hiv. i found a home there, and i started accepting who i am — a queer, hiv+ patient with multiple intersecting identities, and a settler immigrant who experienced depression and used and injected drugs. i could be who i was in a supportive environment, and that was a life-changing experience for me.
 christian hui is a toronto-based hiv+ activist and social worker who is dedicated to bringing awareness to hiv stigma and the importance of treatment. supplied
christian hui is a toronto-based hiv+ activist and social worker who is dedicated to bringing awareness to hiv stigma and the importance of treatment. supplied

hiv/aids and covid have similarities

i also went back to school to study social work, and learn how to provide programming services and research showing the greater involvement or meaningful engagement of people living with hiv/aids (mepa). i will be serving as one of several north american representatives on the ngo delegation to the unaids programme coordinating board (pcb). as global activists, we engage and represent the needs of civil society and represent people living with hiv in key priority population groups. it’s never been more important as we’re experiencing the effects of the dual hiv/aids and covid-19 pandemics. hiv has been a global pandemic for over 40 years, but the word “pandemic” was never really applied to hiv/aids. we need to recognize that hiv/aids and covid-19 have lots of similarities, and that the two pandemics disproportionately impact communities that have often been historically oppressed. from an activist standpoint, we don’t have vaccine equity. covid-19 has taken the forefront of resources and news media, while people don’t really talk about hiv and aids quite so much anymore. that needs to change.
story continues below

advertisement

as as an hiv+ person with suppressed viral loads, we are the safest groups of people to have sex with, you cannot contract hiv from us. but that is not necessarily celebrated. why haven’t governments around the world come together to bring about an overall solution? everyone in the world who is living with hiv should already have access to medication. we need to recognize that u=u is prevention and it is positive. using this campaign to de-stigmatize hiv can encourage the promotion of universal treatment access. we, as a global community, need to come together and invest in our collective health, we must place it and the structural determinants that support people to thrive and be healthy as major societal and political priorities.
as people living with hiv, we know what the gaps are, and i think a lot of times within this new liberalized world order — the way a lot of pressure has been placed on innovation — funding priorities don’t always align with our needs. there are many organizations that cannot address the intersectional needs of the members of their community, and as a bipoc person, there’s this sense that we always need to be repeating ourselves. so there’s a lot of tension because funding has not increased, and support organizations are often competing against each other. on that note, a lot of activists are pushing for community-led monitoring, which means creating our own independent mechanism to assess whether the needs of our peers are actually being met. it’s one way our community can hold organizations and funders accountable.
story continues below

advertisement

doing the work i do now, after the journey i went through, is an honour and a privilege. it’s also very humbling to be able to support this community. i started out as someone who didn’t really know what activism means and so being able to provide opportunities and mentorship is an amazing feeling. it’s made me who i am.
sadaf ahsan is a toronto-based culture writer, editor and stereotypical middle child. she can be reached here.
thank you for your support. if you liked this story, please send it to a friend. every share counts.

comments

postmedia is committed to maintaining a lively but civil forum for discussion and encourage all readers to share their views on our articles. comments may take up to an hour for moderation before appearing on the site. we ask you to keep your comments relevant and respectful. we have enabled email notifications—you will now receive an email if you receive a reply to your comment, there is an update to a comment thread you follow or if a user you follow comments. visit our community guidelines for more information and details on how to adjust your email settings.