Fresh Air - The Forgotten Heroes Of The AIDS Crisis
Episode Date: February 1, 2024Kai Wright's WNYC podcast, Blindspot, revisits the early years of the HIV/AIDS epidemic, focusing in particular on populations that are frequently overlooked — including the pediatric patients at Ha...rlem Hospital.Learn more about sponsor message choices: podcastchoices.com/adchoicesNPR Privacy Policy
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This is Fresh Air. I'm Tanya Mosley.
You've probably heard the comparisons, the height of the COVID pandemic to the early days of the HIV-AIDS crisis.
Millions of people have died from both diseases.
Both ravaged communities and exposed the fault lines in medical care.
Well, in a new podcast series from WNYC and the History Channel,
journalists Kai Wright and Lizzie Ratner take us to New York in the mid-80s when the HIV virus first took root.
So new, it didn't even have a name.
Hi.
So nice to meet you.
Valerie Reyes Jimenez remembers how it all started.
This block has changed so much.
Or at least when they first started to notice it.
We said that people had the monster because they had that look.
They had the sucked-in cheeks.
They were really thin.
A lot of folks were saying, oh, you know, they had liver cancer.
You know, they had cancer.
That's what they died from.
Because you couldn't name it yet.
You called it the monster, or grid,
or in another part of town, maybe the gay plague.
Mostly, though, you avoided talking about it at all
until you just couldn't anymore.
People just started, like, disappearing.
Like, one day they were there, and the next day they were gone.
These 20 people that used to hang out in this building shooting up, they're all gone.
You know, like, car wash, bopple, tear sew, you know, coco-wee.
And, like, all these people, they're all gone.
Like, where did they go?
That was an excerpt from the new podcast, Blindspot, The Plague in the Shadows, co-hosted by our guest today, Kai Wright. Now in its third
season, Blindspot covers overlooked or misunderstood events of our past that continue to shape our
present. Kai Wright is also host and managing editor of Notes from America with Kai Wright.
Before WNYC, Wright was an editor for The Nation and the editorial director of Color Lines. His writing has appeared in several publications, including The New York Times, Mother Jones, and Salon.
And Kai Wright, welcome to Fresh Air.
Thanks so much for having me.
Blind spot is a concept that is exactly that, the things that we overlook or cannot see, you go to places that we've not heard many stories about when we
look back at history during the start of the HIV AIDS crisis. A pediatric ward in Harlem,
a drug market in the South Bronx, a woman's prison in upstate New York. And we're going to talk about
some of what you illuminate in this podcast. But I first want to know, how did you choose which places to go and to focus on?
A lot of the stories are set in New York City
because certainly for the early part of the epidemic,
New York was an epicenter of the documented epidemic.
But the places that we were particularly interested
in talking about are places that
allow HIV to teach us about our society. So this has always been, and it remains, HIV,
this epidemic, it's a roadmap of our social inequities, and our bigotries, yes, but also our political and economic choices
about who is expendable.
And that's been true at the majoritarian level
as a country, as a globe,
but it's also true within communities most affected,
within the LGBT community, within the black community.
And so as a consequence,
the people who have been most affected are often
also the people who have been most undocumented in the storytelling and least talked about.
And so we wanted to go back, we wanted to tell some of the stories that came out of those
communities. And in doing so, help us see more pointedly the ways in which this epidemic,
really, it's a medical crisis, but really, it's a map of our social inequities.
Well, let's start with the perception of HIV-AIDS as a gay disease early on,
and how that impacted public messaging about the threat. You interviewed Dr. Lawrence K. Altman.
He's a longtime science reporter with the New
York Times and a doctor who is credited with writing one of the first mainstream media reports
about HIV and AIDS. The date of his first article is July 3rd, 1981. I want to note, you want to
make a point that there were other media outlets, smaller outlets, those that were focused on LGBTQ
communities that were reporting this out.
But this was one of the first mainstream reports.
And the title of that article was Rare Cancer Seen in 41 Homosexuals.
But as you lay out in this podcast, that's not exactly the full scope of what doctors were seeing.
Even Altman, who also worked at a hospital. What did he share
with you? Yeah, he and many others we've talked to, and this is now well documented, were seeing
in public hospitals and in places that served drug users, provide services to drug users, you know, going back as late as the late 70s,
we're seeing the same constellation of symptoms that would become known as AIDS,
and that were first reported in gay and bisexual men, specifically in Los Angeles, and then
the Bay and then New York City. And so folks were seeing this, but it's hard to answer fully as to why
people were unable to connect the dots between what they were seeing in populations of people
who were injection drug users in particular and their sexual partners. So we were talking about a lot of women of color and poor women of color and what they
were seeing in those gay men. It was really the first glaring blind spot in this epidemic.
And I think there's something interesting in the conversation with Larry Altman. And I want to be
very super clear that the goal is not here to
blame him for something. He wrestles with it. Sure. He was very reflective in the podcast.
Yeah. You know, of what did we see and why didn't we see it? And he was, you know, he was reporting
on it. You know, he was reporting on the epidemic period, which is, you know, not what most of
journalism was doing. So he is to be lauded for that.
But what his reporting became part of was, as you say, this larger feedback loop that strongly linked
this disease to gay men. You actually asked him, did he wrestle with the limitations of what the
CDC had established at the time versus what he was actually seeing. I think he was working at
Bellevue Hospital and he was seeing IV drug users, women. What did he say about that? Because I think
it was really interesting also, it's a commentary on journalism and its role in disseminating
information at that time. Well, you know, I mean, what he said was that this was, he was reporting
the facts and the facts as they were being given to him by the Centers for Disease Control.
And one of the dynamics of not only this epidemic, but conversations about healthcare period is this notion that the men in white coats at the front of the room are the experts.
And their expertise is the beginning and the end of fact about health.
And so what the CDC was saying was received wisdom.
But the CDC had limited vision.
You know, it's funny because what the cdc was
reporting it was a self-reinforcing set of facts um that you know when the cdc would report on the
cases amongst gay men the purpose of that is to tell the health world hey this thing is happening
so people who saw cases among gay men would come back to the CDC and say, yes, I see it.
And so that became this self-reinforcing loop about this is about gay men, not about anybody
else. You also spoke with Anthony Fauci, who in the early 80s was the director of NIA,
the National Institute of Allergy and Infectious Diseases. What did he say upon reflection on the heavy focus of gay men
and maybe discounting or just not including the information on what doctors were seeing and
communities were seeing? You know, he said, listen, and I think this is fair and just. He said,
listen, it's the same lesson we've learned with COVID, to bring COVID again into the conversation, is that this was something that was developing rapidly. It was something that we had never seen before.
And we didn't know what we didn't know. And that part of science and part of public health
is that we are responding to these things in real time and learning things in real time.
And what they knew in, you know,
July of 1981 when Larry Altman published that article in the New York Times or in June of 1981
when the CDC first reported these cases was very different than what they knew even a year later.
And that is true. I mean, I, you know, I think one of the interesting facts here is the rapidity
with which the official data did start to catch up with
reality. I mean, it was within, you know, by the end of the following year, they were starting to
acknowledge, you know, oh, this is, there's an epidemic amongst drug users. There's an epidemic
amongst women. There's an epidemic amongst, there's a pediatric AIDS epidemic. We were starting to see those things as they learned it, but it is so
both instructive and sad and frustrating to think about. Nonetheless, this narrative that locked in
at the beginning, how a set of things that aren't true that can lock into our public imagination, that this was just a gay epidemic, could stick with us to today. One of the epicenters during those early days
was the Pediatrics Department of Harlem Hospital. It became known worldwide when Princess Diana
visited the hospital in the late 80s. Before we listen to a bit from the podcast,
remind us of how children with HIV were perceived
and really how little information doctors had on the reasons
most of these children had the virus.
Well, there are kind of two things going on in the 80s
dealing with children with HIV.
I mean, on one hand, to the degree that people are talking about the idea
that children have HIV,
they are the innocent victims of the epidemic.
And people will remember the name Ryan White, perhaps,
who was the 13-year-old boy
who was contracted HIV through a blood transfusion in Indiana and in 1985
was barred from going to his school because he had AIDS and became kind of the face of
young people, innocent people with AIDS.
And so that's one conversation that's happening.
But the other part of that, the reality of the epidemic amongst children with HIV is there are people who are being born with it.
And they're being born with it because, in many cases, their mothers were injection drug users or had sexual relationships with injection drug users and were HIV positive.
They were poor women of color.
And this was the height of the crack epidemic,
we have to remember.
And those infants who were being born with HIV
were being separated from their parents
and were living and dying their whole lives
on hospital wards.
And Harlem Hospital is one place where that was happening,
more so than anywhere else in the country.
Right. I mean, you talked with Dr. Stephen Nicholas,
who was a pediatrician there.
He told you that Harlem had the highest rate of mother-baby AIDS.
I want to play a clip from your conversation with him.
He's one of many who told you about a four-year-old child named James who was a patient there. In this clip I'm about to play, Dr. Nichols
is talking about those last days of James's life. Let's listen.
I suppose we all felt that he was our child because we were all part of the family.
But death was never far away.
HIV affects the brain, can affect the brain, and he lost his developmental milestones.
So he lost the ability to walk, and then he lost the ability to walk,
and then he lost the ability to talk.
What did he end up passing, though?
Because I know...
Pneumonia, I believe.
Ten level F, right?
Yeah, that would make sense,
because at the time of his passing,
treatments were so...
We didn't know.
We really didn't.
They were just being put together,
and so he probably, you know, wasn't on the standard,
because there wasn't a standard.
Two months before his fourth birthday,
James died in Harlem Hospital.
And I realized that I had to hold a funeral,
and that the family was, in fact, the Harlem Hospital,
and virtually the entire hospital knew about James.
That was a clip from the new WNYC and History Channel podcast, Blindspot,
which looks at the realities of the HIV-AIDS crisis
during those early days of the epidemic.
Kai, James, as you lay out beautifully in this
podcast, really stole everyone's heart. He was one of those kids, as you mentioned, who spent his
whole life there. There was actually a name for these kids. Yeah, they were called border babies,
as in boarding at the hospital. You know, this was one of the provocations for this project in general.
My reporting partner, Lizzie Ratner, who is from New York, spent her whole life here watching the
epidemic and learned about the idea of border babies. And it was one of the things where she
said, well, I've never heard of that. Why haven't I heard of that? And wanted to learn more. And
we talked for years about it before we started reporting on it. And this story, this piece of the story is both really hard when you think about
kids like James, who, as you said, he lived, he was born in Harlem Hospital. He lived his entire
life, all four years of his life on that ward. He only left the hospital once. One time,
he managed to go outside and he died there. These are really difficult stories. But honestly, also,
Tanya, I have to say, it's one of the more uplifting stories also for me because the people
at Harlem Hospital, and this is one of the real, when you ask why I report this podcast, why I tell this story now, is no matter where you enter into this history, you find these incredible human beings who just did above and beyond to take care of human beings, who led with love to take care of other human beings when institutions were failing.
And Harlem Hospital is, the Pediatric Ward of Harlem Hospital is exhibit A of that.
This is a place where we had seen enormous public divestment from that hospital and from
that neighborhood period since the fiscal crisis in New York City in the 70s through
to when the epidemic emerged and at the time when they were
caring for these children. They had very few resources. The stigma was out of control. People
did not want to have anything to do with people with AIDS, including these kids. And the nurses
and doctors on that ward used their own money, their own time to literally create a home for kids like James.
There's a nurse we meet.
She recurs in the podcast.
I have fallen in love with this woman, Maxine Frere.
Yeah.
And she was one of the lead nurses on that floor.
She worked at Harlem Hospital for 40 years.
And she spent her whole life in Harlem.
So her family lived nearby.
And when she would
come home, her family would ask her to take off all of her clothes at the front door because she
was working with AIDS. I just can't help but think about also the nurses and doctors during COVID who
had these same types of relationships with their patients. These nurses and doctors did something,
as you say, that at the time was not happening.
They would touch these children. Even that basic human instinct of touching
someone who had HIV and AIDS during that time was a big deal. And they tried to treat these children.
That's right. And they were not considered essential workers. They were not considered heroes at the time.
They were considered pariahs, the health care workers, you know, to their families and to their communities, if they were thought about at all.
They did this work without any of the applause. I mean, that's another thing that has just been so clear as we've reported this, is just the wounds are fresh still 40 years later.
Let's play a clip from Maxine and Monica.
They both were longtime nurses at Harlem Hospital.
And in this clip, Maxine describes the relationships they had
with the parents and the children.
We lost so many kids.
It was completely mind-numbing.
We actually had set up a bereavement clinic
where the kids would tell us what they wanted to have when they died,
how they wanted to die, what clothes they wanted to have on, you know.
One little boy wanted me to be in his bed with him
and his mother and his grandmother, and so we did.
We knew so little in the beginning.
It was really like walking through a minefield.
The death was hard. It was hard on all of us.
But I think the preparation helped us get through a lot of it.
You know, being able to talk about it amongst ourselves,
because we needed to have a little counseling sometime ourselves,
crying all the time, was very difficult.
They trusted us.
They trusted us emphatically.
I think most of them...
I remember one little boy said,
if I didn't have HIV, I wouldn't have met you guys.
He said, I wouldn't have met you. That was a clip from the new WNYC and History Channel
podcast, Blind Spot, which looks at the realities of the HIV AIDS crisis during those early days of
the epidemic. Let's take a short break. If you're just joining us, I'm talking with Kai Wright,
host of Blind Spot, The Plague in the Shadows, about the early days of the HIV-AIDS crisis, a podcast produced by the History Channel and WNYC Studios.
We'll continue our conversation after a short break. I'm Tanya Mosley, and this is Fresh Air.
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Today we're talking to Kai Wright, host of Blindspot, The Plague in the Shadows,
which takes us to New York in the mid-80s and 90s when the HIV virus first took root.
Kai Wright is the host and managing editor of Notes from America with Kai Wright.
His journalism focuses on social, racial, and economic justice.
Previously, he was an editor at The Nation and the editorial director of Color Lines.
Kai, in your reporting, you highlight the explosion of activism that happened towards the latter half of the 80s and into the 90s. And
one of those activists was Dr. Margaret Haggerty, who ran the pediatric ward at Harlem Hospital.
She helped turn the tide of public sentiment by sharing publicly what they were seeing there.
But then there was this somewhat painful part of all of this, because there had to be a label of innocence, as one of the folks you talked to said, for the tides to turn, for the public to have compassion for those suffering from HIV and AIDS.
There was the Ryan White Care Act fulfilled? Or how did that change and shift our understanding
of the needs of HIV and AIDS patients at the time? Well, there are a few things happening.
On one level, because of a range of activism, some of which is familiar to people, ACT UP
was founded in 1987. And that kind of very public pressuring
of the federal government, but also the people like Margaret Haggerty, who were, I mean, she's
literally throwing these, the deaths on her pediatric ward in the face of federal officials,
you know, and saying, you know, you never cared about public
hospitals, you've never cared about poor people. And so now we're seeing the outcome of that as
you don't care about these children dying. That kind of activism is happening. And then there's
also an activism that's happening in the black community at that time that's exploding, where
we're starting to see black gay men convince members of Congress and other
important civil rights leaders to care about HIV. So there's this convergence of activism that
starts to turn the tide in 87 to force the federal government at least and some state governments to
snap to and say, oh yeah, there is a here, and we are going to have to do something. And so you start to see policy. And one of those really important pieces
of policy is the Ryan White Care Act that's passed in 1990. And it remains a really important part
of the American response to HIV. It funds care and treatment for poor people, essentially.
And it is notable that that law is named after Ryan White, a 13-year-old boy who got HIV through a blood transfusion.
And he is really the epitome of innocence in this epidemic.
He is the person that people can say, he's the type of person who can say, you didn't do anything to bring this on yourself. And that framework,
as from 87 forward, I would argue, we're still struggling with it today. The idea that, okay,
we can start to respond to this, but only for the people who didn't deserve it. For these drug users, for these
promiscuous gay men, for people who brought this on themselves, for the mothers of those children
at Harlem Hospital, they are considered vectors of disease as opposed to victims.
And to put this into perspective, this was also during the time of the war on drugs. So there was a vilification of people who were drug users. of the – because it was the crack epidemic and we had entered into a period where child welfare agencies were stepping into hospitals and saying, you know, we have to separate this child from that parent without a lot – from not only that parent but that family without a real meaningful conversation about what could happen to this child other than being separated from their
family.
Are there other family members who might care for them?
And so they had developed this idea of a social hold, which I think is really instructive
to how the drug war shaped this epidemic, where if a mother was flagged as someone that the state
did not trust to take care of her child, then a social hold was put on the newly born child
to not be allowed to leave the hospital. And that's how you ended up with border babies in
the first place. And you certainly cannot separate this epidemic from the fact of the drug epidemic of the 80s
and the political response to the drug epidemic of the 80s and the criminalization
response of the drug epidemic of the 80s it worsened the reality for individual families
and it got in the way of all kinds of responses that could have shortened this epidemic, quite frankly.
I mean, one of the things that I think people don't wrap their heads around
is there's a part of this epidemic that didn't need to happen at all.
You know, the drug war is directly responsible
for the epidemic amongst injection drug users.
At one point, half of all the injection drug users in New York City were HIV positive.
Wow.
Half.
Half.
And that is a direct consequence of the fact that during the 70s, there was a shift to
saying, okay, we're going to have a policing response to the heroin crisis.
And a number of states, including New York, outlawed the possession of syringes. You weren't allowed to have works in your possession. And what that led to was the creation of shooting galleries that we now response to the fact that it was illegal to have
works. And so cops could stop you on the street. And if you had worked, they put you in jail. And
so people would get together and share the same needle in the shooting galleries. And it became
one of the most efficient ways that HIV spread on this planet was in those shooting galleries.
And it led to those kind of alarming numbers. That is, that is, so that is the drug war and the choices we made about how to deal
with drugs directly causing huge amounts of death. And then when we came up, when, when,
when public health started to come up with the idea of, okay, well, there's no reason for these
needles to be the vector for people getting infected, and came up with the notion of syringe
exchange, which is something we have now, it took so long for that to actually become legal,
because of the mentality about those people are bringing it on themselves. And so we can't have
a public health intervention. We can't we can't have a public health intervention.
We can't treat drug use as a public health problem and just simply allow them to have
clean needles. And once we did that, it went from 50% to 3% infection rates.
Wow. I mean, that's astounding.
There are particular lessons like that where our bigotries, our punitive attitude towards people who are in need
have caused disease in this country. And HIV is a sadly excellent example for us to look at,
to see that process. If you're just joining us, I'm talking with Kai Wright,
host of Blindspot, The Plague in the Shadows, about the early days of the HIV-AIDS crisis,
a podcast produced by the History Channel and WNYC Studios.
We'll continue our conversation after a short break. This is Fresh Air.
Today, we're talking to Kai Wright, host of Blindspot, The Plague in the
Shadows, which takes us to New York in the mid-80s and 90s when the HIV virus first took root. Kai
Wright is the host and managing editor of Notes from America with Kai Wright. His journalism
focuses on social, racial, and economic justice. Previously, he was an editor at The Nation
and the editorial director of Color Lines. Your co-host Lizzie Ratner delves into the research
for treatment and support, which was squarely focused on men during that time. And we've
learned so much about bias and healthcare. It was sort of astounding
to hear in the podcast how women had to fight to convince their doctors to even give them an HIV
test. But in December of 1990, thanks in part to activists, there was a breakthrough, a conference
with the National Institutes of Health about HIV in women, and then studies started to come out. And then we started to see advances in treatment.
But even with this progress during that time period, we're talking like the 90s into the early
2000s, you were reporting on the epidemic during that time.
Disparity over access to medicines was still pretty significant. Yeah. I stepped into covering this epidemic in the mid-'90s.
I was a young black gay man just out of college finding my sexuality.
And this epidemic had been a ghost in my life since I was 12 years old.
And at that moment,
it was a really interesting moment to step into it because this is 1996.
Anti-retroviral therapy becomes available.
The drug therapy that has kept people alive
began to really hit the market and become available.
And we saw death rates just drop dramatically. And that was a moment of celebration, certainly in the gay male
community, where people were literally getting up off of the deathbed. I mean, that's some of the
stuff that when I first started covering this and thinking about it as a reporter, what I was covering were people getting up literally out of their deathbeds to live long and healthy lives.
But not across all populations.
This is also the moment that we see a divergence that now defines this epidemic, where people, if you have access to, the simplest way to understand
it is if you have access to the healthcare system, politically, culturally, economically,
in all the ways, if you have access, HIV was becoming and now has become something that
exists in the background. And if you do not, then HIV remained as deadly and as virulent as it was in 1985.
And so in black communities, particularly in the South, amongst young black gay men, amongst poor black women, The epidemic at that time,
we used to make the comparison,
there was data that you could,
if you took that part of the epidemic
in the United States out,
it was statistically more comparable
to the epidemic in sub-Saharan Africa
than it was to the epidemic anywhere
in the Western world,
which is to say places,
it was more like places
that had very limited healthcare systems
than it was to the richest country in the world.
There's also what was happening
within black and brown communities
around stigma and understanding.
I want to play a clip from an upcoming episode. Parnessa Seal
worked at Harlem Hospital collecting data on AIDS. And as a reminder, Harlem Hospital treated
primarily Black and Latino patients. And Seal talks about grappling with the lack of support
from Black community groups, specifically the church, during those early days. Let's listen to her account of what
it was like. And my work took me on the floor, and people wanted to be, they wanted to be visited.
They wanted someone to pray with them. They wanted someone to hold their hand. And I was there. I
didn't want to do it. And I'm like, where's the church? Because I'm looking at the church that I grew up in in Lincolnville.
When you're sick, you know, mama and the pastor and them, they're rushing to the hospital. And that was just not happening.
That was Pernessa Seal on the new podcast Blindspot, The Plague in the Shadows, talking about what she wasn't seeing in the hospital, support from the church, which has
historically been one of the foundational community centers for Black people. She decided to mobilize
what she called the pew and not the pulpit. What did she end up doing?
Parnessa Seal is truly one of the heroes of the AIDS epidemic.
And she is a woman who, as you heard,
was of deep faith,
who was working at Harlem Hospital as a social worker and an epidemiologist,
and didn't see the church, the black church,
doing what she knew it could do.
And so she just started organizing, pastor by pastor, the black church, doing what she knew it could do.
And so she just started organizing pastor by pastor, congregation by congregation.
Her first step was she decided, okay, well, we just need to have what she called a Harlem week of prayer for the healing of AIDS.
And she went around Harlem and she got as many faith leaders and as many congregations as she could convince to show up for a day at Harlem Hospital and pray with her and walk around Harlem Hospital in prayer for the people inside it. the force of her personality and the force of her tenaciousness and the fact that she
was reaching her peers, that she knew something about the church, the black church and how
it functions, that she was able to begin turning the tide.
I mean, there are now thousands of faith institutions in her coalition all around the world.
Whereas at the time time that first year,
she managed to get 50 to show up, which is a big number for the first time around.
But she has been one of the people, one of, who are really responsible for changing a lot of the
conversation in the church. And listen, I grew up in the black church. It's been a humongously important part of
my life. And I know the kind of caretaking that can happen because there are so many instances
in my childhood I can remember where somebody from my mother's church, from my church,
intervened in some way in my life to make me safe when my parents weren't around.
And that is something that just did not happen as this epidemic began to ravage the Black
community.
40% of people living with HIV today are Black.
Let's take a short break.
If you're just joining us, I'm talking with Kai Wright, host of Blind Spot, The Plague in the Shadows, about the early days of the HIV AIDS crisis, a podcast produced by the History Channel and WNYC Studios.
We'll continue our conversation after a short break.
This is Fresh Air. fresh air. What did people like Parnessa run up against when she tried to get people in the Black
Church involved in helping people who had AIDS? It's really what one scholar puts to us,
describes as a hierarchy of respectability, is what she ran into. And the idea that there are people in our community who are engaged in irresponsible
behavior that brings disrepute on themselves and on all of us at a time of crisis, a broader crisis
around the Reagan agenda, around the crack epidemic, where the community had many crises,
and these people were considered making it worse.
And so they had brought it on themselves and they did not deserve empathy or love.
And her challenge and the challenge of other activists, other black activists like her,
was to reverse that thinking, was to say, these are our brothers and our sisters and uh and and in many cases us is the funny thing um and we have to uh and we have
we have to love each other um that was that was her real core challenge you know and she talks
about it was bad enough the stigma was significant enough that funeral homes refused to bury
black funeral homes you know one of the the big institutions of a place like Harlem
are the funeral homes, because this was one of the places that black people could get
economic advancement throughout the years of segregation was through creating our own
funeral parlors. Did churches refuse services? Absolutely. Absolutely. There became a whole genre of queer activism in particular that is the AIDS funeral, because people would have to come up with their own ways to celebrate people who had been lost. erase everything about that person's life that they found shameful. They would erase the fact
that they were queer. They would erase the fact that they had HIV. They would say they died of
cancer. They would say they died of tuberculosis, of things other than HIV. And so then in the act
of burying them, dehumanize them. And that was a profound and real part of what was happening,
not only in the black community, but certainly in the black community.
And that's what Parnessa had to undo.
And she talks about how like funeral directors come to her now and say, you know, she talked to a particular funeral director who comes to her now and says, you know, I want to repent for the way I behaved at that time.
And as Parnessa says, that's great.
But you cannot go back and fix this.
You cannot go back and reverse what happened then.
We carry those scars.
Kai, you've been deep in this work for a long time.
You also came of age, like me, during the crisis.
How did the AIDS and HIV crisis impact you and your understanding of yourself and the world growing up?
I, as you probably do, Tanya, have deeply imprinted in my emotional memory the moment
I thought, oh, this has something to do with me.
That's 1985.
I was 12 years old.
I remember I was laying on the floor of my grandmother's living room,
watching the news with my uncle. And he was sitting behind me on the couch. And the news
breaks of Rock Hudson, the actor Rock Hudson has AIDS. And he would die later that year.
But in that moment, it was about him and having the diagnosis. And my uncle says,
he literally cannot believe it. He says, there is absolutely no way that Rock Hudson has AIDS
because he is not gay. Now, he used more colorful language than that. I won't sully your ears
with the exact quotes. But the point was, there are two things happening
there. One, disbelief that this could be a thing, because this person, Rock Hudson, who they saw
as heterosexual, could not possibly be gay. And so the ability to disbelieve is just really
striking in that moment. But for me, for me, as I was laying there, I knew,
oh, this has something to do with me. Did you know you were gay at the time? I did not. I could not
have told you that. I'm 12 years old. I'm starting to struggle with things that I wouldn't be able
to articulate, feelings that I wouldn't be able to understand until I was in my 20s. But nonetheless, I knew this has something to do with me.
And from that moment to this day,
this virus has been intimately tied to love and to lust
and to intimacy and to my sexuality.
And that is true for probably three generations of certainly gay men at this
point. It has been such a presence. Through this podcast, you also kind of opened up a portal for
people to understand that there are a significant number of people who are still walking around carrying the grief of the magnitude
of loss during that time period. I think about just when I look at old videos of New York during
that time period, the late 70s, early 80s, the art, the culture. And the first thing that always
comes to my mind is so many of those artists,
so many of those dancers, so many of those people who are contributing to society are no longer here.
Yeah. We have lost so much and continue to lose so much. The people just five years older than me,
the men who, particularly the black gay men who I was turning to for mentorship as I was coming out, and you talk to them, and they were everybody they knew.
They're whole social circles.
They're lovers.
People who just assumed they themselves were going to die. I have a friend and colleague who I worked with for a long time on HIV,
Phil Wilson, who's, you know, was one of the people who really led that movement in the black community. And he has been HIV positive since 1981. He's done a lot of very tenacious activism.
And in the course of this podcast, after knowing him for decades, I asked him for the first time
about like, you know, Phil, you're a kind of person who can be a little relentless. You know, you don't let up. What
is that about? And he said to me, for me, that's my trauma. I felt like if I stop, I'm going to die.
Wow.
You know, and if I stop, everybody I know is going to die.
Kai Wright, thank you so much for this conversation.
Thank you so much for it.
Kai Wright is the co-host of Blindspot, The Plague in the Shadows.
He's also host and managing editor of Notes from America with Kai Wright.
To keep up with what's on the show and get highlights of our interviews,
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Fresh Air's executive producer is Danny Miller.
Our technical director and engineer is Audrey Bentham.
Our interviews and reviews are produced and edited by Amy Sallet, Phyllis Myers, Roberta Shorrock, Anne-Marie Baldonado, Sam Brigger, Lauren Krenzel,
Heidi Saman, Teresa Madden, Seth Kelly, and Susan Nakundi. Our digital media producer
is Molly C.B. Nesper. Thea Chaloner directed today's show. I'm Tanya Mosley.