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D.C. prepares to host Int’l AIDS Conference

Event expected to draw more than 30,000 to city from July 22-27

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Gay News, Washington Blade, HIV/AIDS

Julie Scofield, executive director of the National Alliance of State and Territorial AIDS Directors (Blade photo by Michael Key)

The International AIDS Conference is expected to draw more than 30,000 people from around the world to D.C. July 22-27.

Former President Bill Clinton, former first lady Laura Bush, Bill Gates of the Bill and Melinda Gates Foundation, Health and Human Services Secretary Kathleen Sebelius, U.S. Global AIDS Coordinator Eric Goosby, “The View” co-host Whoopi Goldberg and singer Elton John are among those who are scheduled to speak at the Walter E. Washington Convention Center. The White House has yet to confirm whether President Obama will attend; California Rep. Barbara Lee and Michel Sidibé, executive director of UNAIDS, are among those who are scheduled to speak at the opening session on July 22. The Gay Men’s Chorus of Washington is also slated to perform.

“We are gathering at a defining moment in the AIDS epidemic where the science tells us we can turn the tide on HIV,” said Dr. Elly Katabira, president of the International AIDS Society who serves as the conference’s international chair, and Dr. Diane Havlir of the University of California-San Francisco, who is the U.S. co-chair of AIDS 2012, in a statement that officially welcomed delegates to the nation’s capital. “Scientific advances are also propelling towards the efforts to find a cure and vaccine for HIV. AIDS 2012 will unite science, community and leadership from around the globe to develop strategies and mobilize support for translating new evidence into meaningful action that reflects HIV’s complex web of social, human rights and political issues.”

The conference — the theme of which is “Turning the Tide Together” — will feature a number of workshops and other events that will specifically discuss the epidemic’s impact among men who have sex with men and other LGBT communities. These will include networking spaces in the Global Village that will allow LGBT people and MSM to share strategies to more effectively respond to HIV and advocate on behalf of those living with the virus. “The Lancet” will also present a symposium on the epidemic’s impact among MSM on July 24.

Debbie McMillan of Transgender Health Empowerment will be among the panelists on a July 26 plenary that will examine the virus’ effects on at-risk populations. A symposium on the same day will discuss the future of HIV prevention and related health and human rights issues among gay, transgender and MSM communities.

The Blade is also an official media sponsor of the conference and will host a photo exhibit chronicling AIDS in Washington in the Global Village, which is open to the public.

A call to action

The International AIDS Society and the University of California-San Francisco on Tuesday unveiled a nine-point plan designed to further combat the global epidemic.

The “Washington, D.C., Declaration” specifically calls for an end to stigma, discrimination and human rights abuses against people with the virus and those who remain at-risk for HIV. It backs what it describes as evidence-based prevention, treatment and care that respects the human rights of “those at greatest risk and in greatest need.” The declaration further stresses the need for accelerated research on new HIV prevention initiatives, treatments and a vaccine.

UNAIDS noted in its 2010 report that an estimated 33.3 million people around the world live with HIV. The agency further reported that the number of new infections has fallen 19 percent since 1999. UNAIDS also found that 5.2 million of the estimated 15 million people with the virus in developing countries who need antiretroviral treatment receive it.

“In a scenario unthinkable just a few years ago, we now have the knowledge to begin to end AIDS in our lifetimes,” said Katabira, professor of medicine at Uganda’s Makerere University. “Yet, at this moment of extraordinary scientific progress and potential, the global response to AIDS faces crippling financial challenges that threaten past success and future progress. Through this declaration, we stand together to call on world leaders across all sectors to provide increased resources, visionary leadership and a full-fledged commitment to seize the opportunity before us.”

This year marks the first time since 1990 that the International AIDS Conference has taken place in the United States—President Obama in 2009 completed the process that lifted the ban on people with HIV from entering the country. City officials and HIV/AIDS service providers alike plan to use the biennial gathering to highlight local efforts to combat the epidemic.

D.C. Officials, HIV/AIDS groups seek presence at conference

The Department of Health’s HIV/AIDS, Hepatitis, Sexually Transmitted Disease and Tuberculosis Administration will present 15 scientific abstracts on the epidemic during the conference. The D.C. Center for AIDS Research, the body that coordinates HIV/AIDS-specific research in Washington, will highlight city-based research in a Global Village session. Mayor Vincent Gray is among those who will speak at a Memorial AIDS Quilt ceremony on July 22.

“It’s appropriate that AIDS 2012 is taking place in the District, its first return to the U.S. in 22 years, as the District has in so many ways been the face of our nation’s epidemic,” said D.C. Council member David Catania (I-At Large.) “From years of an inadequate and failed response to now, an increasingly effective and aggressive one, the District embodies the varied and diverse experience our nation has endured with the deadly disease. AIDS2012 will be a fantastic opportunity for the District to showcase its innovative prevention and treatment programs for the best and brightest in the field. The District stands as an example of what can occur when data-driven, evidence-based policies are put in place.”

Whitman-Walker Health will hold a forum on the state of the epidemic at the Lisner Auditorium, where the city’s first AIDS forum took place in 1983, on July 24. Metro Teen AIDS and Us Helping Us have also scheduled a series of events to coincide with the conference. Organizers have also organized tours of Helping Individual Prostitutes Survive, Food and Friends, La Clinica del Pueblo and other D.C. HIV/AIDS service organizations for delegates.

“We are pleased and honored to have the International AIDS Conference come to D.C.,” Dr. Ray Martins, chief medical officer at Whitman-Walker, told the Blade. “The conference gives the world a chance to learn more about the state of HIV/AIDS in the District of Columbia, but also the breadth of the response to the epidemic locally. It will allow us to highlight the tremendous efforts made by outreach workers and volunteers as well as health care providers and our elected officials.”

A number of gatherings, panels and other events will also take place throughout the city in the days leading up to the conference. These include the Gay Men’s Health Summit at George Washington University and the Global Forum on MSM and HIV on July 21, a panel on stigma in transgender and other HIV-vulnerable communities at the Human Rights Campaign on July 21 and Youth Force’s annual conference at Gallaudet University in Northeast Washington from July 17-19 and the International Network of Religious Leaders Living with or Personally Affected by HIV/AIDS’ conference at Howard University from July 17-19.

“It’s really an incredible event, so I’m glad it’s coming back here,” Ron Simmons, president of Us Helping Us, told the Blade. “With the eyes of the world focused on you, this is the time to take advantage of it.”

Calls to bolster response to domestic epidemic

HIV/AIDS activists also plan to use the conference to urge lawmakers in this country and around the world to reaffirm their commitment to ending the epidemic.

The Rev. Al Sharpton, journalist Tavis Smiley and former Atlanta Mayor Andrew Young are among those scheduled to speak at the “Keep the Promise” March that will wind its way from the Washington Monument to the intersections of 3rd Street, N.W., and Constitution and Pennsylvania Avenues, N.W., on July 22. Members of the We Can End AIDS coalition told the Blade earlier this month that they plan to hold a five-point march on July 24 that organizers said could end in acts of non-violent civil disobedience.

Policy makers also plan to urge Congress to adequately fund policies they say effectively combat the domestic epidemic.

“When people think of AIDS today, most probably don’t realize that AIDS is still really in a crisis mode in our country,” said Carl Schmid, deputy executive director at the AIDS Institute, during a press conference at the National Press Club in D.C. on Tuesday. He noted that 20 percent of the 1.2 million Americans with HIV today do not know their status. Schmid also pointed to roughly 50,000 new diagnoses each year. “Many, including our youth, have become complacent. With nearly 40 percent of new infections occurring in those under age 29 and with more HIV in our country than ever before, it is imperative that we raise our country’s consciousness.”

President Obama in 2010 unveiled a National HIV/AIDS Strategy that seeks to reduce rates of HIV and HIV-related health disparities and increase access to care for people with the virus.

Under the White House’s proposed budget for fiscal year 2013, funding for HIV prevention programs would increase by $40 million. The president also seeks a $75 million increase in funding for the AIDS Drug Assistance Program under the Ryan White Comprehensive AIDS Response Emergency Act.

Julie Scofield, executive director of the National Alliance of State and Territorial AIDS Directors, applauded the Obama administration for what she described during the National Press Club press conference as its ongoing commitment to fight the domestic epidemic. She stressed, however, that federal funding has not kept pace with the needs of those with HIV.

“It has always been important to acknowledge from the very beginning of this fight that the goals of the strategy cannot be achieved without significant increases in funding for critical domestic HIV/AIDS discretionary programs,” said Scofield.

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District of Columbia

Trans activists arrested outside HHS headquarters in D.C.

Protesters demonstrated directive against gender-affirming care

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(Photo by Alexa B. Wilkinson)

Authorities on Tuesday arrested 24 activists outside the U.S. Department of Health and Human Services headquarters in D.C.

The Gender Liberation Movement, a national organization that uses direct action, media engagement, and policy advocacy to defend bodily autonomy and self-determination, organized the protest in which more than 50 activists participated. Organizers said the action was a response to changes in federal policy mandated by Executive Order 14187, titled “Protecting Children from Chemical and Surgical Mutilation.”

The order directs federal agencies and programs to work toward “significantly limiting youth access to gender-affirming care nationwide,” according to KFF, a nonpartisan, nonprofit organization that provides independent, fact-based information on national health issues. The executive order also includes claims about gender-affirming care and transgender youth that critics have described as misinformation.

Members of ACT UP NY and ACT UP Pittsburgh also participated in the demonstration, which took place on the final day of the public comment period for proposed federal rules that would restrict access to gender-affirming care.

Demonstrators blocked the building’s main entrance, holding a banner reading “HANDS OFF OUR ‘MONES,” while chanting, “HHS—RFK—TRANS YOUTH ARE NO DEBATE” and “NO HATE—NO FEAR—TRANS YOUTH ARE WELCOME HERE.”

“We want trans youth and their loving families to know that we see them, we cherish them, and we won’t let these attacks go on without a fight,” said GLM co-founder Raquel Willis. “We also want all Americans to understand that Trump, RFK, and their HHS won’t stop at trying to block care for trans youth — they’re coming for trans adults, for those who need treatment from insulin to SSRIs, and all those already failed by a broken health insurance system.”

“It is shameful and intentional that this administration is pitting communities against one another by weaponizing Medicaid funding to strip care from trans youth. This has nothing to do with protecting health and everything to do with political distraction,” added GLM co-founder Eliel Cruz. “They are targeting young people to deflect from their failure to deliver for working families across the country. Instead of restricting care, we should be expanding it. Healthcare is a human right, and it must be accessible to every person — without cost or exception.”

(Photo by Cole Witter)

Despite HHS’s efforts to restrict gender-affirming care for trans youth, major medical associations — including the American Medical Association, the American Academy of Pediatrics, and the Endocrine Society — continue to regard such care as evidence-based treatment. Gender-affirming care can include psychotherapy, social support, and, when clinically appropriate, puberty blockers and hormone therapy.

The protest comes amid broader shifts in access to care nationwide. 

NYU Langone Health recently announced it will stop providing transition-related medical care to minors and will no longer accept new patients into its Transgender Youth Health Program following President Donald Trump’s January 2025 executive order targeting trans healthcare. 

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CMS moves to expand HIV-positive organ transplants

HIV/AIDS activists welcome potential development

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Earvin 'Magic' Johnson, right, and NMAC CEO Harold Phillips speak at the 2025 U.S. Conference on HIV/AIDS in D.C. (Washington Blade photo by Michael Key)

The Centers for Medicare and Medicaid Services is pushing forward a proposed rule that would make it not only easier for people with HIV in need to get organ transplants from HIV-positive donors, but also make it a priority where there was often a barrier.

The Washington Blade sat down with people familiar with this topic — from former heads of the Centers for Disease Control and Prevention, to HIV activists and to the first HIV-positive person to donate an organ — about what this proposed change could mean.

HIV is a virus that attacks the body’s immune system, particularly targeting the body’s T-cells, which makes it harder to fight off infection and disease. If left untreated, HIV can become AIDS. Without treatment, AIDS can lead to death within a few months or years. The virus is spread through direct contact with bodily fluids — often through sex, unclean needles, or from mother to baby during pregnancy.

According to HIV.gov, a website managed by the U.S. Department of Health and Human Services, approximately 1.2 million people in the U.S. were living with HIV in 2022. Of those 1.2 million, 13 percent don’t know they have it.

The virus disproportionately impacts men who have sex with men and people of color.

The CDC’s statistics show men are most affected, making up almost 80 percent of diagnoses, with gay and bisexual men accounting for the majority. Racial disparities also are present — Black people make up 38 percent of diagnoses. The World Health Organization estimates that around 44.1 million people have died from AIDS-related illnesses globally as of 2024.

Since the virus was first detected 45 years ago, scientists have been working on ways to treat and prevent its spread. In 1987, the first breakthrough in fighting HIV came as the U.S. approved the first HIV medication, AZT — marking the beginning of antiretroviral therapy. This medicine — and later descendants of it, like today’s widely prescribed Biktarvy — stop the HIV virus from reproducing and allow the body to keep its T-cells.

Then in 2012, another big step toward minimizing the scope of the potentially fatal disease came as the CDC approved the first HIV prevention medication, Truvada, more commonly known as PrEP. As of 2024, nearly 600,000 people in the U.S. are using PrEP, according to AIDSVu, which uses data from Gilead Sciences (manufacturers of Truvada and Biktarvy) and is compiled by researchers at the Rollins School of Public Health at Emory University.

The following year, in 2013, the HIV Organ Policy Equity (HOPE) Act was signed into law, enabling the use of organs from HIV-positive donors for transplants into HIV-positive recipients, overturning a 1988 ban.

There are an estimated 123,000 people waiting for organ transplants in the U.S. The number of HIV-positive people on that list is estimated to be smaller, harder to precisely quantify, but they are still in dire need.

A study from the New England Journal of Medicine, published in 2024, analyzed the outcomes of 198 kidney transplantations to people with HIV at 26 medical centers across the U.S. from 2018 to 2021.

Results from the study showed that for kidney transplants performed using organs from 99 donors with HIV and 99 without HIV, one-year survival rates for HIV-positive recipients were nearly identical (94 percent and 95 percent, respectively). Three-year survival rates were also similar (85 percent and 87 percent). Organ rejection rates were also numerically on par after three years (21 percent and 24 percent). Other measures for surgical outcomes, including the number of side effects that occurred, were also roughly the same for both groups.

This shows that, overall, HIV-positive-to-HIV-positive transplants are nearly identical in outcome to transplants between HIV-negative donors and recipients.

Where we are now

Now in 2026, CMS is pushing past the clinical trial testing phase it has been in, making HIV-positive-to-HIV-positive organ transplants more widespread and more accessible.

Adrian Shanker, the former deputy assistant secretary for health policy and senior advisor on LGBTQ health equity at HHS, explained to the Blade that the HOPE Act was a step in the right direction, but this policy change from CMS will expand the ability to help HIV-positive patients in need.

“The original HOPE Act asked for scientific research,” Shanker explained. “There were 10 years of clinical trials. The Biden administration promulgated a rule that removed clinical trial requirements for kidney and liver transplants between people living with HIV. This proposed rule is further implementation on the CMS side with the organ procurement organizations to ensure they’re carrying out the stated intent of the HOPE Act law. It’s building on consensus that has existed through multiple administrations.”

The proposed change would go into effect on July 1, and, according to Shanker, would help everyone in need of an organ — not just HIV-positive people.

“People living with HIV, their ability to receive organs from other people living with HIV in a more streamlined way means that the overall organ waitlist is sped up as well,” he added. “So it benefits everyone on the waitlist.”

Shanker, who was also a member of the Presidential Advisory Council on HIV/AIDS, spoke about how this is a rare moment of bipartisanship.

“There’s no secret that the Trump administration has been quite adversarial to LGBTQI plus health, and to the health of people living with HIV/HIV prevention resources as well … From destabilizing PEPFAR to shutting down one of the primary implementation partners, which is USAID, to firing almost the entire staff of the Office of Infectious Disease and HIV Policy at HHS … But what this is is a glimmer of hope that we can have bipartisan solutions that improve quality of life for people living with HIV.”

Harold Phillips, the CEO of NMAC, a national HIV/AIDS organization that pushes policy education and public engagement to end the HIV epidemic, and an HIV-positive American, sees this as a huge gain for the HIV-positive community.

“For a number of years, we were excluded from that pool of potential donors,” Phillips said. “Many people living with HIV were excluded from being able to get organ transplants. So this opens up that door. This is a positive step forward that will help save lives.”

That “open door,” Phillips said, does more than just provide life-saving organs to people in the most need. It provides a sense of being able to support their community.

“I remember when I was no longer able to check that box on my driver’s license,” Phillips recalled during his interview with the Blade. “I remember what that meant — that my organs might not be able to save a life. The potential that now they could is really exciting for me.”

“To think about people living with HIV donating their organs to other people living with HIV and helping extend their health and well-being — that’s an exciting moment in our history. It reinforces that HIV is not a death sentence anymore.”

Human Rights Campaign Senior Public Policy Advocate Matt Rose also sat down with the Blade to explain the realities of HIV-positive people in the U.S. right now who are looking for a transplant.

“If you’re HIV positive and on the waitlist for an organ right now, your chance of getting one is slim to nil,” Rose said. “This at least gives you a real shot.”

He went on to explain that while the HOPE Act started to move in the right direction, it hasn’t done enough for HIV-positive people in dire need.

“This bill [HOPE] was supposed to fix that — and it never really has. But every administration, we keep chipping away at the next hurdle,” he said. “This latest move will drastically expand the ability for someone who is HIV positive to donate an organ.”

That slow chipping away, in addition to the non-stop trials being done to prove the efficacy and ability for HIV-positive people’s bodies to accept organ donation, is part of the broader push to normalize this practice and remove outdated restrictions.

Shanker elaborated, explaining all that time was necessary to figure out the efficacy of HIV-positive-to-HIV-positive organ transplants but now that the data has been collected — its time to expand the availability.

“There were over a decade of clinical trials between the original HOPE Act law being signed by President Obama and our rule being promulgated at the end of the Biden administration. It was to allow those clinical trials to run their course,” Shanker said.

Nina Martinez is the first HIV-positive person to donate an organ to another person with HIV.

She explained that the stigma and lack of understanding from the general public is another hurdle that those working to improve the quality of life for people living with HIV have to deal with.

“People don’t generally understand that treatment works,” Martinez said, who became the first person to undergo HIV-positive organ donation in 2019. “When you have access to antiretroviral therapy, it lowers the virus in your bloodstream to levels so low that lab tests can’t detect it. Clinically, that correlates to good health and an inability to transmit HIV sexually. I was healthy enough to pass the same evaluation as any other living donor without HIV.”

She continued explaining:

“Just by having a diagnosis of HIV, they’re labeling donors as medically complex, and that’s not accurate. Every donor with HIV has to pass the same evaluation as donors without HIV,” she said. “If someone passes that evaluation and still isn’t allowed to donate, that’s discrimination. If a patient is willing to accept that organ and you block it because of preconceived notions, you’re denying someone care based on disability. That runs counter to basic fairness.”

When asked about her decision to become a donor and what message she hopes it sends, Martinez emphasized that the choice should remain personal.

“I didn’t undertake this endeavor to say that people with HIV should donate. This is a community that’s been through a lot and has contributed to science — we have served. But for people who wanted a way to leave a legacy, and that is what I wanted, they should be supported in that. There shouldn’t be arcane scientific perceptions and myths getting in the way of that.”

National Donor Day, which raises awareness of organ donation, is on Feb. 14. To become an organ donor, visit registerme.org.

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CVS Health agrees to cover new HIV prevention drug

‘Groundbreaking’ PrEP medication taken by injection once every six months

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CVS Health, the nation’s second largest pharmacy benefit manager company that plays a key role in deciding which drugs are covered by health insurance policies, has belatedly agreed to cover the new highly acclaimed HIV prevention drug yeztugo.

The U.S. Food and Drug Administration approved the use of yeztugo as an HIV prevention or “PrEP” medication in June 2025 as the first such drug to be taken by injection just once every six months. AIDS activists hailed the drug as a major breakthrough in the longstanding effort to end the HIV epidemic.

“We are pleased that CVS Health has finally decided to cover this groundbreaking new PrEP mediation,” said Carl Schmid, executive director of the HIV+ Hepatitis Policy Institute.

“Four months ago, 63 HIV organizations joined us in sending a letter to CVS’s president urging them to reconsider their refusal to cover Yeztugo and reminding them of their legal obligation to cover PrEP and describe the important benefits the drug would bring to preventing HIV in the U.S.,” Schmid said in a statement.

He noted that CVS Health now joins other leading pharmacy benefit manager companies and insurers in covering yeztugo. Gilead Sciences, the pharmaceutical company that developed and manufactures yeztugo, has said 85 percent of all people with health insurance in the U.S. now have coverage for the drug, according to Schmid.

“However, coverage does not automatically translate into access and usage,” Schmid said in his statement. “Too many people are being forced to pay copays while other payers, including employers, are failing to cover all forms of PrEP,” he said.

According to Schmid, the HIV+ Hepatitis Policy Institute is joining other HIV advocacy organizations in urging federal and state government officials to engage in “aggressive enforcement of PrEP insurance coverage requirements and sustained funding of state, local, and community HIV prevention programs.”

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