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Supervisor Kuehl on historic LGBTQ death data collection order

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It’s an old adage: you don’t know what you don’t know. To which might be added: you won’t find out if you don’t care. All of which makes the motion passed Sept. 3 by the Los Angeles County Board of Supervisors historic, moving and possibly precedent-setting.

LA County became the first local government body in the nation to pass a motion requiring culturally competent trained medical examiners and coroners to investigate violent deaths— including suicides, hate crimes, and homicides—to see if they involve the LGBTQ community, to collect data on the victim’s sexual orientation or gender identity data, and regularly report back to the Supervisors so they might develop better prevention and safety policies.

“Most of what I know, I get from CSI shows or those kinds of things where medical examiners are quite prominent” in determining if and what kind of crime occurred, out Supervisor Sheila Kuehl tells the Los Angeles Blade.

“This adds another kind of layer to the work that they already do, which is, if possible, to identify that this is a subpopulation group that we want to look at specifically,” Kuehl says. “Sometimes, it can help and sometimes, we’re not sure what to do about it. But we do want to be able to create greater understanding and protection of, especially, trans women who have been very vulnerable to violence and murder. I think that this is just the beginning.”

In fact, the motion says: “The work of the Medical Examiner and Coroner’s [Office] is vital, as it often is used to gather evidence and information that can be used in a criminal proceeding. However, this work can also highlight disparities in mortality rates, and provide valuable insight that can be used to guide policies, resources, and law enforcement efforts to protect at-risk communities.

“Many Medical Examiner and Coroner’s offices, including our own, do not currently collect and aggregate data pertaining to sexual orientation and gender identity,” the motion says. “In the absence of this data, it is impossible to detect the presence of disparities in mortality rates of the LGBTQ community. By tracking this data, it will allow us to better understand these disparities and develop policies that seek to address them at the County level.”

Kuehl co-authored the motion with Supervisor Kathryn Barger, who succeeded her former boss, conservative Republican Mike Antonovich. But while Antonovich had a reputation for being anti-LGBTQ, Barger has long appeared to be an LGBTQ ally. Kuehl says she cares “deeply” about the LGBTQ community.

LA County Supervisors Sheila Kuehl and Kathryn Barger (Via Barger’s Facebook page)

“Because [Barger’s] not part of the community or in a community that’s part of the community, I think the data about suicide among our young people in our community, about murder and violence against trans people and the data about how much higher a percentage of our young people are in the foster care system than exist in the general society—it came to her a little bit later than I had seen it,” Kuehl says.  “She was very moved by it and just decided that it was something we wanted to know about in the county.”

Barger’s original motion “asked Dr. Lucas, our coroner, who’s also the chief medical examiner, just to develop a plan for collecting the data because it’s not always clear what a person’s sexual orientation might’ve been or motive if it’s a hate crime, etc. We need to know how we’re going to do that,” says Kuehl.

Additionally, Barger directed them “to hire a consultant or a subject matter expert to do tightening in the department. If there’s any way, in terms of sensitively, to figure out… if there’s a way to even help collect this data without asking somebody’s parents, which would not always be sensitive. Then, we want a report back every three months on how they’re coming along figuring this out. It seemed like a reasonable way to start collecting the data, and a very, very necessary thing because we have no real data in the county to back up our larger understanding of the experience in the community.”

One source for the data that so impacted Barger was The Trevor Project, which just updated their statistics in time for the new school year. The Trevor Project’s 2019 National Survey on LGBTQ Youth Mental Health reported that of 34,000 LGBTQ youth surveyed, 39% of LGBTQ youth seriously considered attempting suicide in the past 12 months, with more than half of transgender and non-binary youth having seriously considered. “The same study found that 14% of LGB youth had a suicide attempt in the previous 12 months, rising to 29% for transgender and nonbinary youth,” the motion reported.

“Lesbian, gay, bisexual, transgender and non-binary youth are more than 4 times more likely to attempt suicide than their peers, so it’s imperative for school suicide prevention policies to also be LGBTQ competent. In addition, our research shows that more than half of LGBTQ youth are not out to a single adult in school; these policies show LGBTQ youth, out or not, that their school is a safe place for them to learn, and that school staff are prepared to help them in times of crisis,” said Sam Brinton, Head of Advocacy and Government Affairs for The Trevor Project.

The motion also cited the current data for hate crimes. “The Federal Bureau of Investigation’s (FBI) statistics show that in 2017, 7,175 hate crimes were reported, 1,130 of which were based on sexual orientation bias and 119 on gender identity bias. According to the National Center for Transgender Equality, one in four transgender people have been assaulted simply because they are transgender. The report went on to say that of these incidents, the majority of deadly attacks against transgender people are against women of color,” the motion reported.

Though press stories on the motion tend to emphasize LGBTQ youth, Kuehl says “they’re not going to limit themselves here. But we will probably ask them to aggregate the data by age, as well, because it is important when we have so many youth in our foster care and juvenile justice system who identify as LGBTQIA. It’s important for us to know because the outreach that we do or the work that we do in the Department of Children and Family Services, in Probation, in the Office of Diversion and Re-entry, which has a juvenile division now—we want to have some sensitivity to the community, as well. So, we’re probably going to slice and dice the data, but it won’t be limited” to youth.

First, staff needs to be trained to be able to figure out how they can collect the data. “The core for us, actually, is to see if we need additional or different kinds of services that the county can provide to help, particularly, with messages about suicide prevention that could be more targeted, working with outside entities, like Trevor. We already have an LGBTQ youth project in five departments where I ask for a report back every quarter about how they’re improving their services and sensitivity about this youth population,” says Kuehl.

“It’s not like we know what we’re going to do with it yet, but we do have these other projects that could incorporate new data,” Kuehl continues. “We might also want to make certain that we have some idea about safety in our various areas in the county. No one is ever safe from being attacked and harmed. You just can’t watch everybody at every minute, but there may be something. We could see there’s a zip code where trans people are more in danger or something.

“There are a lot of touchpoints in the county,” Kuehl says, “but I don’t think they will analyze the experience of our community in terms of why. What we can only try to do is aggregate data and take it for the truth and try to work with it.”

Let that sink in. LA’s local governmental body—the most populous county in the country with more that 10 million people—wants to collect LGBTQ data and “take it for the truth” instead of erasing LGBTQ data at the federal level. Perhaps the idea might catch on.

Reminder: September is Suicide Prevention Month. If you, or someone you care about, is in a crisis, call the Suicide Prevention Lifeline at (800) 273-8255 or text “Home” to 741-741 or call The Trevor Project 24/7 at 1-866-488-7386 or text START to 678678.

 

 

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Fentanyl Crisis

Federal health officials hold roundtable on opioid overdose crisis

“Deaths caused by opioids like illicit fentanyl are preventable with naloxone,” said White House advisor Dr. Rahul Gupta

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HHS Secretary Xavier Becerra, Rahul Gupta, Tammy Baldwin, Robert Calif and Miriam Delphin Rittmon at Whitman-Walker Health (Washington Blade by Lou Chibbaro Jr)

WASHINGTON – U.S. Department of Health and Human Services Secretary Xavier Becerra and four other high level federal health officials held a roundtable community meeting followed by a press conference at D.C.’s Whitman-Walker Health headquarters on Friday to discuss what they said were “groundbreaking” efforts to address and end the nation’s epidemic of deaths from the overdose of opioid drugs.

A statement released by HHS says Becerra and the other officials, including Dr. Rahul Gupta, director of the White House Office of National Drug Control Policy, reached out to Whitman-Walker, which, among other things, operates one of the D.C. metro area’s preeminent substance abuse treatment programs, to commemorate the one-year anniversary HHS’s Overdoes Prevention Strategy program.

“Now, one year after the release of this strategy, our nation is in a much stronger position to treat addiction and save lives,” Becerra said. “We didn’t get here by accident. Thanks to decades of work by advocates, coupled with an unparalleled people-first strategy and unprecedented investment by the Biden-Harris administration, we have made a great deal of progress,” he said.

The officials, including Gupta, pointed out that the Overdose Prevention Strategy over the past year and an updated effort launched this month have focused on greatly expanding availability of the drug overdose antidote medication naloxone.

“Deaths caused by opioids like illicit fentanyl are preventable with naloxone, and today’s announcement means more life-saving naloxone will be in communities across the country,” Gupta said. “The latest data continue to show a hopeful trend of a decreases in overdose deaths, so we must remain focused on fully implementing President Biden’s National Drug Control Strategy that will save tens of thousands of lives by expanding care for substance use disorder, making naloxone more accessible, and dismantling drug trafficking operations,” he said. 

In addition to Gupta from the White House, Becerra was joined at the community meeting and press conference by Dr. Miriam Delphin-Rittmon, assistant secretary for the Substance Abuse and Mental Health Services Administration (SAMHSA), which is an arm of HHS; Dr. Debra Houry, acting principal deputy director of the U.S. Centers for Disease Control and Prevention and Dr. Robert Califf, commissioner of the U.S. Food and Drug Administration. 

Also participating in the roundtable session and press conference was U.S. Sen. Tammy Baldwin (D-Wis.), the nation’s first out lesbian member of the Senate. 

Becerra said he invited Baldwin to participant in the day’s events, among other things, because of her record of advocacy and support for funding of federal substance abuse and overdose prevention programs. 

“One area I’ve championed in Congress is increasing access to overdose reversal medication like naloxone,” Baldwin said. “We know that when you increase access to this safe and effective treatment that you save lives,” she said. “And I’m thrilled to see the Biden administration and especially the Food and Drug Administration taking steps to increase access to naloxone.”

Califf told the gathering one of the FDA’s recently launched efforts is to work with drug manufacturers to arrange for naloxone to become an over-the-counter drug that would further expand its availability. 

The roundtable discussion session, which included close to 50 participants, including Becerra and the other federal officials, was closed to the press, according to an HHS spokesperson, because among those participating were Whitman-Walker clients and others who receive services and support for what the officials called substance use disorder.

During the press conference that followed, Becerra spoke of how some of those participating in the roundtable discussion were part of Whitman-Walker’s success stories in helping people overcome substance use problems 

“We’re here because a year ago we decided to go in a different direction at the federal level,” he said at the press conference. “We decided that we’re not moving fast enough, we’re not moving close enough to where we need to be to try to help communities and those folks at Whitman-Walker who are trying to not just get folks into treatment but to save lives,” Becerra said. 

“And that was the great thing about the round table that we just had,” he said. “We heard about how people thrive,” he said, adding, “And one of the clients, Deborah, spoke about how she’s on the verge of getting her degree from college … That’s what we want to see … I want to thank the folks at Whitman-Walker for letting us come today to see how people can thrive and be part of that success.”

Whitman-Walker Health CEO Naseema Shafi told the Washington Blade after the press conference that Whitman-Walker has a long history of partnering with federal government agencies in addressing health issues, including Whitman-Walker’s role as a healthcare facility welcoming the LGBTQ community. 

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AIDS and HIV

Patti LaBelle, Gladys Knight dazzle World AIDS Day concert 

“As millions remain affected by HIV/AIDS, World AIDS Day provides an opportunity to honor those we’ve lost and those living with HIV/AIDS”

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Patti LaBelle performs onstage during World AIDS Day 2022 at John F. Kennedy Center for the Performing Arts on November 30, 2022 in Washington, DC. (Photo by Paul Morigi/Getty Images for AIDS Healthcare Foundation)

WASHINGTON – The AIDS Healthcare Foundation (AHF) hosted its 2022 World AIDS Day Concert on Wednesday, Nov. 30, in the concert hall of The John F. Kennedy Center for the Performing Arts in the nation’s capital.

Renowned multi-Grammy Award-winning vocalists Patti LaBelle and Gladys Knight delivered show-stopping performances to the packed crowd, which included supporters, dignitaries such as: Harold Phillips, Director of the White House Office of National AIDS Policy; White House Senior Advisor for Public Engagement, Mayor Keisha Lance Bottoms, Congresswoman Sheila Jackson Lee, and New Orleans Mayor, Mayor LaToya Cantrell, and more, in a night of hope and celebration.

The legendary Gladys Knight performs at the Kennedy Center during a free concert hosted by AHF to commemorate World AIDS Day on December 1, 2022, in Washington.
(Joy Asico/AP Images for AIDS Healthcare Foundation)

AIDS Healthcare Foundation (AHF), is the world’s largest HIV/AIDS care provider, currently operating in 45 countries. The concert is held every year to commemorate World AIDS Day, observed internationally each year on Dec. 1. This year also marked the global organization’s 35th anniversary. 

At the event, longtime humanitarian and AIDS advocate, Princess Diana was honored, posthumously, with AHF’s Lifetime Achievement Award. Under its “Keep the Promise!” banner, AHF also acknowledged progress made in the global fight against HIV and AIDS and continues to raise awareness about “The Other Pandemic” as a reminder of the significant work still to be done on HIV/AIDS, as well as remembering the lives that have been lost over the years.  

Legendary entertainers Patti LaBelle (L) Gladys Knight (C) and AHF President Michael Weinstein, together at The Kennedy Center during a free concert hosted by AHF to commemorate World AIDS Day on December 1, 2022, in Washington.
(Joy Asico/AP Images for AIDS Healthcare Foundation)

Michael Weinstein, President of AHF, said, “As millions remain affected by HIV/AIDS around the globe, World AIDS Day annually provides an opportunity to honor those we’ve lost and those living with HIV/AIDS today, as well as reminding leaders and the community of the work that still remains to address this epidemic. From providing compassionate AIDS hospice care in those darkest early days to growing to become the largest global AIDS organization today, now providing lifesaving care and treatment to more than 1.7 million people around the globe, we also celebrate the tireless work of all those who help make today’s AHF possible: our staff, Board, affiliate organizations and affinity groups, friends, family and elected officials and community partners across the globe, but most of all, our clients and patients—with our annual 2022 World AIDS Day event. It was a momentous night to host our World AIDS Day concert at The Kennedy Center for the first time, and welcome back the legendary Patti LaBelle, and have another great American icon, Gladys Knight join us, while also being able to honor the legacy and humanitarian work of the late Princess Diana.”

President of AIDS Healthcare Foundation, Michael Weinstein and Director of the White House Office of National AIDS Policy, Harold Phillips attend World AIDS Day 2022 at John F. Kennedy Center for the Performing Arts on November 30, 2022 in Washington, DC.
(Photo by Paul Morigi/Getty Images for AIDS Healthcare Foundation)
Congresswoman, Sheila Jackson Lee and Patti LaBelle attend World AIDS Day 2022 at John F. Kennedy Center for the Performing Arts on November 30, 2022 in Washington, DC.
(Photo by Paul Morigi/Getty Images for AIDS Healthcare Foundation)
Derek J. attends World AIDS Day 2022 at John F. Kennedy Center for the Performing Arts on November 30, 2022 in Washington, DC.
(Photo by Paul Morigi/Getty Images for AIDS Healthcare Foundation)
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AIDS and HIV

Cleve Jones, activist & founder of AIDS Memorial Quilt honored

National AIDS Memorial hosted observances at the 10-acre Memorial Grove and displaying Quilt in nearly 100 communities throughout the U.S.

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Former San Francisco mayor Art Agnos presents award to Cleve Jones (Photo courtesy of National AIDS Memorial Foundation)

SAN FRANCISCO  – The National AIDS Memorial marked World AIDS Day with a national observance at the 10-acre National AIDS Memorial Grove in San Francisco, honoring AIDS activist and founder of the AIDS Memorial Quilt Cleve Jones with its Lifetime of Commitment Award. 

The two days of events brought together leaders on the front lines of the epidemic for powerful conversations and events focused on “Changing the Pattern for a Future without AIDS,” referencing a major initiative of the Memorial that is bringing the Quilt to the South to address the growing crisis of rising HIV rates amount communities of color and marginalized populations.

Jones, who founded the Quilt thirty-five years ago, was recognized for his visionary leadership, activism, and powerful voice in the fight for health and social justice. He remains an inspirational force for change and action today, standing up without hesitation and using his voice for those who are often overshadowed and not heard.  

U.S. House Speaker, Rep. Nancy Pelosi (D-Cailf.) praised Jones in a special video tribute, saying, “Cleve, you are a force of nature – unshakable in the face of adversity, overflowing with a passion for serving others.”

“When the AIDS crisis tightened its grip on San Francisco – when pain and despair grew rampant – you kept hope alive,” she continued. “You were a shining light in the dark, building community out of grief and spurring action out of anguish. From the halls of power to union halls and picket lines, you have never relented in your mission: empowering the oppressed, tearing down injustice and honoring the dignity and beauty of every person.”

Presenting the award to Jones was former San Francisco mayor and mentor Art Agnos to an audience of more than 600 people from the community who gathered on the eve of World AIDS Day for a gala to support the Memorial’s programs. 

“I’m honored to receive this award, but more importantly I’m so pleased that the Quilt now has a permanent home with the National AIDS Memorial and that it is continuing its mission of activism and justice. One thing I’ve learned is that through hope one finds courage and through courage we find love. Love is at the core of what we do and that is what this Quilt represents,” Jones told the audience gathered.

The National AIDS Memorial worked with local partners from across the country to display hundreds of Quilt sections featuring more than 3,500 individual panels in nearly 100 communities on World AIDS Day. 

The largest Quilt display ever in Alabama is taking place in Montgomery and surrounding areas as part of the memorial’s Change the Pattern initiative. The program, funded through a $2.4 million grant from Gilead Sciences, is organizing quilting workshops, displays and educational programming with Southern AIDS Coalition throughout the Southern U.S.

“On this World AIDS Day, it is inspiring to know that thousands of Quilt panels are on display in communities across the country, touching hearts and minds through the stories represented in the fabric,” said Gilead Sciences Chairman and CEO Daniel O’Day.  “The Quilt’s purpose remains as strong and important today, as it was thirty-five years ago, when the vision of Cleve Jones sparked a powerful movement to advance health and social justice.”

The National AIDS Memorial’s World AIDS Day Observance panelists highlighted the importance of the work being done around the country, the interconnectivity of issues to reach zero, and the importance of education and outreach to at-risk populations during three powerful conversations available for viewing online on the memorial’s website and include: Reflections with Cleve Jones and 35 years of the Quilt; The State of the Epidemic Today with Leaders on the Frontlines; and Young Leaders Making an Impact.

 

Reading of the Names at the National AIDS Memorial Grove in San Francisco
(Photo courtesy of National AIDS Memorial Foundation)

“As our community comes together this World AIDS Day, it’s hard not to look around and see who’s missing – our friends, lovers, and family we’ve lost over four decades of this horrific, cruel disease,” said National AIDS Memorial CEO John Cunningham. “It always brings tears, and we carry so many emotions, particularly as we think of what could have been. But for me, as a man living with HIV/AIDS, I shift to a brighter space, choosing to look around me, thinking about so many of us still here, living and thriving. Survivors, who have so much to be thankful for, but also a heavy burden to share our own stories and journey, so history never repeats itself.”

He continued, “Today, people are still dying and there should have been a cure long ago. We are angry because bigotry, hate, and stigma persist today in society.  And we carry shame, because communities of color and marginalized populations continue to be disproportionately impacted by HIV and discrimination, and it shouldn’t be this way.  It’s time to change the pattern.”

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AIDS and HIV

Translatinx network helps a resilient community ‘Live Its Truth’

“We’re trying to push ourselves to the next level through community empowerment and leadership development”

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Courtesy of Cristina Herrera

NEW YORK – When Cristina Herrera was 15 years old, she traveled alone from Southern California to the Bronx in pursuit of new life experiences. A native of El Salvador, Cristina thought as a teenager that she was different, but she was unsure about which terminology fully captured her identity.

“I knew that I wasn’t gay,” explains Cristina. “But I couldn’t put into words as to who I was.” 

It was only through connecting with the trans Latinx community in New York that Cristina found herself – and came out as transgender.

When Cristina began her gender transition in the mid-1980s, she says there were barely any employment opportunities for a transgender person. To survive, many immigrant trans women in Cristina’s circle engaged in sex work and became more susceptible to contracting HIV. Policing and arrests of sex workers also put their immigration statuses in peril, and stigma exposed them to violence. It was during this time that Cristina became set on improving the lives of trans Latinx people.

“My community was already informally supporting one another,” she says. “But I wanted to make sure that other people would never have to go through some of the difficult issues I experienced.”

Determined to fulfill this promise, Cristina put herself through college and landed a job at a nonprofit supporting the LGBTQ+ community. She absorbed as much as she could at the organization, but she started to want a bigger influence on how to serve the community that helped find her identity. 

“In 2005, I began dreaming about starting a trans-led, immigrant-led organization,” she says. “My dream came true two years later when I started the nonprofit.”

Today, as the founder and CEO of the advocacy nonprofit Translatinx Network, she serves trans Latinx people in New York City and beyond. The organization, which for the past three years has been a Gilead TRANScend Community Impact Fund grantee, connects people to legal aid, HIV prevention and support groups, and immigration assistance.

In the years since its creation, Cristina and her colleagues have led the charge in providing support and connections for trans Latinx people as they build their communities in the United States.

“Many people in our community went from being in the shadows to becoming documented and getting their green cards or work permits,” she says. “We were showing our community that we don’t have to be stuck – that there’s more to life.”

Cristina is now looking for ways to replicate the success of the organization by gathering information and its outcomes and continuing to expand its services. “We want to stay on the front lines and keep our community healthy and protected,” she says. “We’re trying to push ourselves to the next level through community empowerment and leadership development.”

And Cristina is proud that through her organization’s success, she’s able to serve a population that has historically been left out or forgotten.

“I love any opportunity where I can be there for others,” she says. “I want all of us to be able to live our truth while at the same time fulfill our life goals.”

The preceding article was previously published by [email protected] © 2022 Gilead Sciences, Inc. and is republished with permission.

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AIDS and HIV

Ending HIV-related stigma in the Southern U. S.: Gina’s story

“Stigma is an onion with many layers,” Gina says. “We can really do this – we really can, but we have to address the layers that drive HIV”

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Blossom Chrishelle Brown (Left) with Gina Marie Brown (Photo Credit: Southern AIDS Coalition)

BIRMINGHAM, Al. – Gina Brown has been living with HIV for 27 years and introduces herself as a social worker by training, but an activist by birth. As the Director of Strategic Partnerships and Community Engagement at the Southern AIDS Coalition, she’s working to fight against challenges that she has personally experienced such as homelessness, addiction and abuse, as well as stigma, racism, sexism and ageism.

“Everything that you could think of when it comes to HIV, I’ve experienced,” she says. “When I’m sitting at the table, I’m not just talking with an employee hat on. I’m talking from a community standpoint as a person on the same journey.”

‘Stigma kills’

Stigma can be a significant barrier to receiving HIV care or medical treatment. A 2021 survey by GLAAD and Gilead shows that the U.S. South not only has the highest rates of HIV diagnosis, but it’s also a region that is generally uncomfortable with HIV. Positive test results, in turn, are too often accompanied by secrecy and isolation.

“Stigma kills. I know that sounds like a cliché, but it’s the truth,” Gina says. “It keeps people out of care. It keeps people from taking their medication. It keeps people from disclosing their status. It keeps people from being happy.”

Stigma impacts people everywhere with HIV, but Gina believes in the Southern United States it’s more than just external stigma. “We internalize what people say and think about us. We get caught up in it and actually think those things about ourselves too.” 

The Southern AIDS Coalition, a Gilead grantee, focuses on stigma reduction and culturally appropriate care. Education and public health advocacy are core to the organization’s goals of preventing new transmissions and building a better life for people living with HIV.

Using deliberate language to discuss HIV is one important tool the coalition uses to help dismantle stigma, Gina says.

“You go in the room, and you might have somebody who will stand up and say, ‘I’m HIV.’ And I say, ‘No, you’re living with HIV.’ That’s the first thing, getting people to understand that we are living, we’re not dying, we’re not sick, we’re not all of those things,” she says.

Power of Community: Sharing HIV Experiences

Gina also helps facilitate a program called “Out of the Shadows,” with the Institute of Women and Ethnic Studies. The group works to provides a safe space for women in the New Orleans community to share their HIV experiences, improve access to services and overcome feelings of isolation. She says it was her own experience with the community that was critical to helping her regain her confidence after being diagnosed.

“What you see now is not always who I was in this fight. It was people who truly carried me and gave me tools to empower myself. People saw things in me that I never saw in myself,” she says.

Gina now wants to serve as that type of person for those she works with, and she always strives to meet them where they are in their journeys. “If you need to crawl, I will crawl with you. When you start walking, I will walk with you.”

But Gina says with a laugh, “When you start running, you’re on your own because I’m too old to run. I’ll do everything else with you, but I’m not running.”

Ending the HIV Epidemic

Efforts by the Southern AIDS Coalition and other organizations to reduce stigma and discrimination have been highlighted by the United Nations as critical to ending the epidemic. Gina looks with optimism toward the end of the epidemic and the UNAIDS goal to get every community and country on track to end AIDS as a public health threat by 2030. 

“Stigma is an onion with many layers,” Gina says. “We can really do this – we really can, but we have to address the layers that drive HIV.”

The preceding article was previously published by [email protected] © 2022 Gilead Sciences, Inc. and is republished with permission.

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AIDS and HIV

Iconic landmarks in Los Angeles to light up red on World AIDS Day

This year’s theme, “Putting Ourselves to the Test: Achieving Equity to End HIV,” calls out the disproportionate impact across sub-populations

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Los Angeles Blade graphic

LOS ANGELES –  As Angelenos mark World AIDS Day, several prominent landmarks around Los Angeles County– including Union Station, City Hall/Grand Park Fountain, Dignity Health Sports Park, LAX Pylons, and Six Street Viaduct — will switch their evening architectural lighting to all red to increase awareness about HIV/AIDS, show solidarity in the fight against HIV, and honor those who have died due to HIV disease.

World AIDS Day, observed each year on December 1, provides the opportunity to honor and remember the more than 40 million people worldwide, including over 27,000 Los Angeles County (LAC) residents lost to HIV/AIDS since this epidemic began.

This year’s World AIDS Day theme, “Putting Ourselves to the Test: Achieving Equity to End HIV,” calls attention to the disproportionate impact of HIV across sub-populations, particularly across race, gender, sexual orientation and geographic lines. 

Los Angeles County has an estimated 59,400 people living with HIV and in 2021 there were 1,479 new HIV diagnoses reported, mostly among gay men, African-Americans, Latinos, and transgender persons.

“We thank our partners across the community who have been working for decades to increase awareness and prevention of HIV/AIDS and provide services and support for those living with HIV, “and honor those in our communities we lost to this terrible disease,” said Barbara Ferrer, PhD, MPH, MEd, Director of Public Health. “More than anything, as we honor, on World AIDS Day, those in our communities we lost to this terrible disease, we re-commit ourselves to the work to end the HIV/AIDS epidemic, which continues to disproportionately impact communities of color and the LGBTQ community.”

Public Health works with others to help bring an end to the epidemic by reducing the number of new annual HIV infections, decreasing the number of undiagnosed people living with HIV, and increasing the viral suppression rates among people who are diagnosed with HIV.

Public Health collaborates with a broad cross-section of diverse community partners to implement community-driven outreach and education, community-based HIV/STD testing, linkage to care, intensive street-based case management, and clinic-based services.  Recently, Public Health has spearheaded innovative programming through our many new Ending the HIV Epidemic (EHE) Initiatives (www.lacounty.hiv), expanded HIV testing access through both community-based partners and the  www.takemehome.com testing initiative, ongoing efforts to prevent homelessness among persons living with HIV; enhanced outreach efforts to the transgender community through our TransInLA Instagram and Facebook pages and supporting HIV-positive individuals with accessing lifesaving medication. Research shows that suppressing HIV to undetectable levels virtually eliminates transmission of the virus to sexual partners.

Public Health encourages people to learn more about HIV, know their HIV status, and, if necessary, access free life-saving HIV medications and services.  To learn more about HIV and STDs and locate HIV testing, services, and resources, please visit www.getprotectedla.com and http://publichealth.lacounty.gov/dhsp/

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