Since the start of this semester, I have been working for
the North Carolina AIDS Action Network. The Elton John AIDS Foundation has graciously
financially supported my work with NCAAN.
After accepting my sexuality as a gay man, one of my biggest
fears became contracting HIV. I come from a low-income, Latino household, one
that used to be undocumented, so there existed many barriers for my family and
I to have access to information that would destigmatize HIV and its
intersection with queerness in our communities.
I had this idea that because I was gay, I would contract HIV
and my family members and loved ones would disown me. The culmination of this
fear was that love with another man would be unattainable.
I have been very lucky to befriend people that have helped
me destigmatize HIV, both in the community and in myself. I have reached a level of comfort where I
can speak on how I can reduce my risk of contracting HIV, not because being HIV
positive would be a lapse in my moral character, but because the working
systems of society have made it difficult for people with HIV to live fulfilling
lives.
While working at Pride events across the state with NCAAN, I
have been able to interact with both HIV positive and negative individuals. These
interactions included me working at booths and passing out information, but
what has been the most moving for me has been the times when people have shared
their status with me, unsolicited.
One of the particular handouts we give at the NCAAN booth
includes a small booklet from a pharmaceutical company that has thirty quotes,
each for a day of the month, of people with HIV that gives insight into a part
of how that individual’s life has changed since they knew their status.
It was one of the pieces of information that moved me the
most. It held genuine pieces of people’s stories. It told me about their fight
for survival in a society that attempted to disown their humanity and push them
further into the shadows, while also letting that person with their newly
discovered status know that they would be content and okay.
One of the goals that we have at NCAAN is to increase the accessibility
of HIV preventative services to individuals across the state. We also relay
information about how to stay “safe,” and we do all as an attempt to decrease
the spread of HIV across North Carolina.
While talking to Matt Martin, one of my supervisors, one of
the most difficult things that we encounter is a way to amplify preventative
information and services, at the same time attempting to discontinue the
stigmatization that being HIV positive is a mark of death – stereotypes that
have harmed the personal relationships and whole lives of individuals in our
LGBTQ communities.
Simultaneously, we tell people to be safe and weary of how
to prevent the contracting HIV, while at the same time telling them that it’s
okay to be HIV positive, and that a full, healthy life is possible.
The most important voice in the act to destigmatize HIV is
the voice of the same people that are being shunned from society. When people
with HIV speak of their experiences, they push, implicitly, the taboo of HIV
into the light of everyday life. We have all probably met someone with HIV,
whether they know it or not, and whether we know it or not. They deserve the
same respect and love that we would expect.
In a society that has consistently asked HIV positive
individuals to feel wrong and embarrassed about their status, these individuals
fight to speak up. Even though the burden is being placed on those that are
already burdened, the weight of that voice allows people
like me to feel comfortable to reach out and reside in an environment that will
allow me to live with health and with love – something that was so far from
reach as a closeted child.
-Erick D. Aguilar, Outreach Analyst Intern for the NC AIDS Action Network
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