U.S. Rep. Henry Waxman
April 13, 1982
First Congressional Hearings on AIDS Begin in Hollywood

Congressman Henry Waxman, whose district includes the gay community of West Hollywood, convenes the first congressional hearings on AIDS at the Los Angeles Gay Community Services Center.

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“I want to be especially blunt about the political aspects of Kaposi’s sarcoma,” said Rep. Waxman, according to the Washington Blade.  “This horrible disease afflicts members of one of the nation’s most stigmatized and discriminated-against minorities…. There is no doubt in my mind that if the same disease had appeared among Americans of Norwegian descent or among tennis players — rather than among gay males — the responses of the government and the medical community would have been different.”

Rep. Waxman made an effort to involve the gay community of his district by holding the hearing at the LA Gay Community Services Center (now the Los Angeles LGBT Center).  But the media largely overlooked the event, and the coverage that did appear was within the LGBTQ press.

The San Francisco newspaper The Sentinel published a very short blurb three days later, titled “House Holds Cancer Hearings.”  The paper would quote an unnamed subcommittee staffer saying the Centers for Disease Control “should not have to nickel and dime” for research funding.

The short article appeared next to a column written by gay nurse Bobbi Campbell, who wrote about going to the Shanti Project to get emotional support for his KS.

Speaking at the hearing, Dr. James Curran, head of the Center for Disease Control’s Task Force on Kaposi’s Sarcoma and Opportunistic Infections, estimated that tens of thousands of people were already infected by the disease.

On the 40th Anniversary of the CDC’s first report on what would become known as AIDS, reporter Karen Ocamb wrote the Washington Blade article “AIDS @40: White House laughs as gays try to save themselves,” recalling the House hearing chaired by Rep. Waxman.

“Like so many others in California, lesbian feminist Ivy Bottini had high expectations for the federal government to finally intervene in the growing AIDS crisis after the first congressional committee hearing on the mysterious new disease,” Ocamb wrote.  “She was upset.  Her friend Ken Schnorr had died just before the hearing and Bottini had to explain to Ken’s distraught mother that he had not been abused at the hospital — the purple bruises on his body were KS lesions.”

Ocamb goes on to cite perhaps one of the most egregious examples of the Reagan administration’s homophobic callousness toward people with AIDS, which happened just weeks after Reps. Waxman and Phillip Burton (D-San Francisco) introduced a bill to fund AIDS research.

On Oct. 15, 1982, White House Press Secretary Larry Speakes was holding a press conference, during which reporter Lester Kinsolving asked Speakes about the new disease called AIDS.  After indicating that he didn’t know what AIDS was, Speakes dismisses the question and makes light of it, saying, “I don’t have it. Do you?”

When this response elicits chuckles from the members of the press corps, Speakes continues in this vein (“There has been no personal experience here, Lester”) to draw more laughter.

“The exchange goes on like that.  For another two years,” Ocamb wrote.

* * * * * *

Washington Blade, “AIDS at 40: White House Laughs as Gays Try to Save Themselves” by Karen Ocamb, June 23, 2021

The Atlantic, “The Heroic Story of How Congress First Confronted AIDS” by Joshua Green, June 8, 2011

September 28, 1982
AIDS Research Bill Introduced (and Dies) in Congress

Congressmen Phillip Burton and Ted Weiss introduce the first legislation for the allocation of funding for AIDS research. Unfortunately, the resolution dies in committee.

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It will be almost one year later, in July 1983, when the first dedicated funding for AIDS research and treatment is approved by Congress.

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www.HIV.gov, “A Timeline of HIV and AIDS”

October 15, 1982
Question about AIDS Draws Laughter at White House Briefing

At White House Press briefing, a reporter asks Press Secretary Larry Speakes: “Does the President have any reaction to the announcement — from the Centers for Disease Control in Atlanta — that AIDS is now an epidemic and has over 600 cases?”

Speakes: “What’s AIDS?”

Reporter: “It’s known as the ‘gay plague.’”

Everyone laughs.

“I don’t have it,” Speakes replies. “Do you?”

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The transcript of the press briefing, which is in the Ronald Reagan Presidential Library, is a sharp reminder of how governmental officials and journalists viewed the LGBTQ community.

On Dec. 1, 2015, Vanity Fair debuted a short documentary by Scott Calonico about this now-infamous exchange.

President Reagan would not mention AIDS until 1985, and then it would be in response to a reporter’s question at a press conference.  He would not give a major speech about the epidemic until mid-1987 — at which point 20,849 people in the U.S. would already be dead.

* * * * * *

The Washington Post“How Attitudes toward AIDS have Changed, in the White House and Beyond” by Juliet Eilperin, December 4, 2013

Washington Blade, “AIDS at 40: White House Laughs as Gays Try to Save Themselves” by Karen Ocamb, June 23, 2021

Vanity Fair, “The Reagan Administration’s Unearthed Response to the AIDS Crisis is Chilling” by Richard Lawson, December 1, 2015

Young Legislative Aide Steers AIDS Policy in California

Gay activist Stan Hadden, a state senate aide, leads the effort in Sacramento to establish the California AIDS Advisory Committee and set up a mechanism for funding AIDS education throughout the state.  The 26-year-old staffer would go on to author much of the state’s HIV-related legislation.

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As a staff member of the Office of then-State Senate President Pro Tempore David Roberti, Haddon would be credited with shepharding the passage of Senate Bill 910, which established the California AIDS Advisory Committee.  The bill included an initial appropriation of $500,000, channeled through the Department of Health Services to some of the state’s community programs which desperately needed funding.  While the amount seems very small, it was an accomplishment to get any funding at this time, during which the state was suffering from a financial crisis and many health programs were forced to reduce their budgets.

“AIDS is a national emergency,” Senator Roberti told the media in March 1983 when promoting the merits of SB 910. “It is occurring in epidemic proportions among previously healthy homosexual men, Haitian immigrants, and intravenous drug users, but 6% of those afflcted with the disease are neither homosexuals, IV drug users, Haitians or hemophiliacs.”

At that time, it was unusual for legislators to be educated about HIV.  The senator’s awareness of the urgent need for AIDS services could be largely attributed to the work and advocacy of his staffer, Hadden, and the location of his district, which was the Hollywood area.

According to Stephen Morin’s chapter “AIDS: Public Policy and Mental Health Issues” in the 1986 book What to Do About AIDS, Senator Roberti’s legislation, which was researched and drafted by Hadden, was the first significant action that California took in the early days of the AIDS crisis.

“SB 910 required a great deal of advocacy,” said Morin, who was an assistant clinical professor at the University of California San Francisco at the time.  “In April 1983, on one of my early trips to the state capital to support that bill, I was joined by Gary Walsh, a friend and psychiatric social worker who had been diagnosed with KS in December 1982.  Although AIDS had recently been the cover story in Newsweek, more than half of the legislators with whom we met had never heard of AIDS.”

Around the same time, the California Assembly pushed forward $2.9 million in additional funding for  the University of California to work on AIDS research.  Speaker of the Assembly Willie Brown, whose district was located in San Francisco, introduced an allocation to the UC budget after convening with university researchers working on discovering the cause of AIDS.

“Many of the early breakthroughs in research came from the UC system and were funded through this effort,” Morin wrote.  “The discovery of the retrovirus responsible for simian AIDS, for example, was discovered at UC Davis.  Later, in Jay Levy’s laboratory at UC San Francisco, a retrovirus responsible for AIDS was isolated.”

In 1985, Hadden would be the staffer behind state legislation to bring a coordinated approach to local HIV/AIDS programs and services.  California Senate Bill 1251 allocated about $17 million in funding for AIDS healthcare programs in 1986.  In addition, the state directed more than $5 mllion of its federal budget toward research projects and epidemiology studies.

Legislative staffers regarded Haddon as the “unofficial AIDS czar” of California.  He was one of only a few in Sacramento who were open about their LGBT identity, journalist Karen Ocamb would later write in The Pride.  Scores of administrative and political aides to California legislators remained in the closet, fearful that open knowledge of their sexual identity would end their professional careers.  Elected officials and potential candidates who identified as LGBT also remained silenced by the very real fear of ruination.

* * * * * *

Los Angeles Times, “Stan Hadden:  Roberti Aide Influenced AIDS Policy,” December 26, 1991

What to Do about AIDS: Physicians and Mental Health Professionals Discuss the Issues, editor Leon McKusick (University of California Press, 1986)

California Budget Analysis, 1986-1987, State of California Health and Welfare Budget

The Pride, “California Legislative Caucus Honors LGBT Pioneers” by Karen Ocamb

May 18, 1983
Congress Passes Bill with AIDS Research Funding

The U.S. Congress passes the first bill with funding targeted for AIDS research and treatment — $12 million for agencies within the U.S. Department of Health and Human Services.

Learn More.

* * * * * *

www.HIV.gov, “A Timeline of HIV and AIDS”

AIDS United, “Our Timeline: Past and Future”

June 17, 1983
NYT Reports on Abandoned Infants with AIDS

Growing numbers of infants infected with AIDS in utero are abandoned in New York City hospitals, according to a New York Times article.

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On Page 22, the Times gives its report on the alarming cases of babies and young children who are born with the AIDS virus and subsequently left at New York hospitals.  The article carries no byline.

The article also exposes the discrepancy between the total number of pediatric AIDS cases nationwide being reported by the Centers for Disease Control (18) and the numbers of infants and children being treated by doctors in the NY metro area alone (more than 63).

In the article, New York pediatric immunologist Arye Rubinstein, M.D., blamed the CDC’s low case number on the federal government’s “unduly strict” definition of AIDS.  Because of this narrow definition, the CDC counted only children who had a malignancy or opportunistic infections.

Dr. Rubinstein told the Times that he was treating several patients whose symptoms did not fall within the CDC definition but most definitely were indications of infection by the AIDS virus.  The article cites Dr. Rubinstein’s pediatric AIDS caseload as consisting of 44 patients.  James Oleske, M.D, of St. Michael’s Hospital and the Newark College of Medicine was cited with a caseload of 18 pediatric patients and six more suspected cases.

In the years to come, Dr. Rubinstein would become very vocal about CDC case totals being undercounted and the need for the CDC to broaden its definition of pediatric AIDS — and he wasn’t the only doctor in the field to do so.  Finally in 1985, the CDC would broaden its defnition of AIDS, based on recommendations developed at the Conference of State and Territorial Epidemiologists, and the CDC would modify the definition again in 1987 and 1993.

The Times article also chronicled the plight of young children with AIDS who had been abandoned in NYC hospitals.  Doctors said the children have been left in hospitals by mothers who had died or are dying of AIDS.

Since the City did not have a place to house parentless AIDS children, they were left in the hospitals that were treating their conditions.  The Times reported that the City’s welfare agency, Special Services for Children, was seeking foster homes for the children, but no one would take them.

This article was among the first to focus on the heartbreaking situation of the population that would become known as “AIDS babies,” children born with the AIDS virus and then orphaned.  In the 1980s, most of these children died within two years.

* * * * * *

The New York Times, “Young Victims of AIDS Suffer its Harsh Stigma,” June 17, 1984

Centers for Disease Control and Prevention, “AIDS: The Early Years and CDC’s Response” by Drs. James Curran and Harold Jaffe, October 7, 2011

National Institutes of Health, “Survival of Children with HIV in the United States has Improved Dramatically Since 1990s, New Analysis Shows,” December 18, 2009

Pat Buchanan column (4)
June 23, 1983
Reagan Staffer Patrick Buchanan Vilifies Gay Men in Op-Ed

Patrick J. Buchanan, President Ronald Reagan’s speechwriter, publishes an op-ed in the New York Post, writing: “The poor homosexuals — they have declared war upon nature, and now nature is extracting an awful retribution.”

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In his op-ed in the New York Post, Pat Buchanan echoes the Moral Majority position that the AIDS epidemic was God seeking revenge against gay people.

Buchanan concluded his essay by saying homosexuals should be banned from food-handling jobs, and that the Democratic party’s decision to hold its 1983 convention in San Francisco will endanger delegates and their families.

Visitors to the city, he writes, will be at the mercy of “homosexuals who belong to a community that is a common carrier of dangerous, communicable and sometimes fatal diseases.”

* * * * * *

ThinkProgress, “Flashback — Buchanan: AIDS is Nature’s ‘Awful Retribution’ Against Homosexuality” by Igor Volsky, May 24, 2011

July 1, 1983
Stanford Blood Bank Begins Screening Donations

Stanford Blood Center institutes the first blood testing program specifically intended to reduce the risk of transfusion transmission of AIDS.

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Between July 1983 and June 1985, a total of 33,831 blood donations were screened by Standord.  Of those donations, 586 were shown to have low CD4 counts and were discarded as possibly infected.

Stanford retained the serum samples from the 586 donations and years later, when a test became available, screened them specifically for HIV.  Dr. Engleman found that 1.9% of these donations were HIV positive — which translates to approximately 33 HIV-infections that were avoided.

As the first blood bank in the U.S. to screen donated blood for HIV/AIDS indicators, the new policy eliminated donations from people with low CD4 T cells.  The loss of CD4 T cells in AIDS is what renders patients susceptible to a wide range of infectious diseases.  Thus, the screening was considered a surrogate test, not necessarily identifying the presence of HIV/AIDS but instead identifying indicators of possible HIV/AIDS infection.

The new screening system came about due to an increasing awareness in the San Francisco medical community of AIDS and a skeptical view toward existing blood protection practices.  In the spring of 1983, Stanford Hospital treated two patients with AIDS.  Both had received transfusions at Bay Area institutions and neither had been identified as being in a high-risk group.

“At this point, my colleagues and I at Stanford Blood Center felt that the presence of the presumed etiologic agent for AIDS in the local blood supply could not be ignored,” recalls Ed Engleman, MD, of the Stanford Blood Center.  “Because of the potential lethality of this infection, we felt that self-deferral should not be relied upon as the sole means of protecting the blood supply.”

The self-deferral practice that Dr. Engleman refers to is the U.S. Public Health Service’s then-recommendation of relying on donors to voluntarily identify themselves as a member of a high-risk group.  Blood centers around the country commonly implemented the PHS recommendation with an information sheet provided to prospective donors that described AIDS risk groups and requested that donors exclude themselves if they met the definition of risk.

“It was predictable that this approach wouldn’t work very well,” says Dr. Engleman.  “First, it relied entirely on donor self-deferral.  Second, the PHS definition of homosexual AIDS risk behavior was vague, making it possible for a prospective donor with a history of homosexual activity to feel that he personally was not at risk for AIDS and to proceed with blood donation.”

Stanford University Blood Bank’s screening procedure was costly and had to be performed manually, but Stanford found it relatively easy to implement because it was already conducting immunological research and had access to a flow cytometer and the appropriate laboratory setting.

Around this time, the American Red Cross, American Association of Blood Banks, and the Council of Community Blood Centers released a joint statement estimating the risk of getting AIDS from transfusion as “one in a million.”  This was an overly optimistic view, it turned out.

Just a few years later, when the first HIV antibody test was made available in 1985, an estimated one in 700 units of blood donations in U.S. metropolitan areas were found to be infected with HIV.  In San Francisco, the frequency was closer to one in 100.

“We estimate that the total number of transfusion-related HIV transmissions that occurred from 1983 to 1985 was at least 10,000-20,000,” Dr. Engleman says.  “It seems evident that most of these cases could have been avoided had our test been used.”

* * * * * *

August 1, 1983
Congress Holds Hearings on U.S. AIDS Reponse

The Congressional Subcommittee on Government Operations holds hearings to examinethe federal response to AIDS.  It would take another four years before the Reagan Administration finally acknowledges the demands of AIDS activists.

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Statement of Michael Callen of New York to Congress
(born April 11, 1955, died December 27, 1993)

In December of 1981 I had some blood testing done by my private physician, and those tests indicated that I was immune deficient. In December of 1981, there was very little known about this disease, but there was in the gay press beginning to be reports of increased instances of very unusual diseases, and they outlined some of the symptoms. I was very concerned because I had some of these symptoms — fevers, night sweats, general lymphadenopathy, swelling of the lymph nodes, malaise, fatigue.  So I had myself tested and, as I indicated, in December of 1981, I was told I was immune deficient.

The effect of being told that I was immune deficient was devastating.  I called my parents and said, “I am going to die.”

I was not hospitalized until the summer of 1982, when I was diagnosed with cryptospordiosis, which is one of the qualifying opportunistic infections, according to the CDC definition of this syndrome.

I was hospitalized for over a week with what is known as the wasting syndrome.  It was the lowest point of my life.  I was convinced from everything I read and heard that I was going to die.

But I recovered from that specific infection, and I was rehospitalized in the fall of 1982.  They suspected pneumocystis pneumonia. I had a bronchoscopy performed and other tests.  It turned out to be bronchitis.  But my story really illustrates one of the consistent stories for people who have this syndrome.  So little is known.

When my doctor indicated to me in December of 1981 that I was immune deficient, I said, “What does that mean?”

And he said, “We don’t know.”

So now a lot of people who are being told they are immune deficient are simply waiting, waiting for the next infection.

Now, I have come to believe that I am going to beat this disease.  I no longer think that I am going to die.  But it is very difficult when you pick up newspapers or turn on the television, and you hear that no one has fully recovered from this syndrome, and that 80% of those diagnosed with the syndrome are dead after two years.

So I guess that is my story — waiting around for infections, checking myself every morning for Kaposi’s sarcoma lesions and waiting for information about this disease to be forthcoming.

Statement of Roger Lyon of San Francisco to Congress
(born September 30, 1948, died November 4, 1984)

I was diagnosed with Kaposi sarcoma on February 3 of this year.  Prior to that time, I was having absolutely no AIDS-related symptoms whatsoever.  On physical exam at that time, three lesions were found internally.  Prior to that, I was being treated for an amoebic disorder, no real symptoms of AIDS.

February 3, basically 100, I think more exactly 180 days ago, I became aware I had a life-threatening disease.  On February 4, I entered UC, I went to University of California without an appointment, at the suggestion of my doctor, and started what is called their staging process — a battery of tests to determine the extent of this disease.

At that time, I was basically numb.  I had no feeling.  I was just moving.  UC has been — they have been very kind and helpful.

However, it is a matter of day-to-day waiting, waiting for something to happen, living in constant fear that I am going to wake up one morning to find lesions, waking up finding that I have some other opportunistic infection, cryptospordiosis, possibly pneumocystis pneumonia.

At this time, I am basically living in fear of what is to come. Other than that, it is a day-to-day wait-and-see process.

Statement of Anthony “Tony” Ferrara of Washington, DC to Congress
(born in 1954, died June 4, 1984

The first idea there was something wrong with me was last summer.  I had lymphadenopathy, swollen lymph glands especially around the jaws and throat and under the arms.  That continued for a few months, but the whole time I felt quite good.  I continued to run and jog, and I experienced no fatigue, no night sweats, no fevers.  In fact, in November, I finished the Marine Corps marathon, when I was supposedly very, very ill.

The lymphadenopathy went away.  So I thought nothing further of it.  But all along, I had been reading about AIDS, and of course, as every conscious gay man should be, was very worried about it.

In February, I saw two small purple lesions, one on the inner aspect of each of my lower thighs, and I knew what they were, or I knew what they could be, and I said I would wait a month, and if they were still there in a month, I would seek treatment or seek a diagnosis.  Well, in the beginning of March they were still there.

I belong to the George Washington University HMO.  I went there and told them that they really should biopsy one of these lesions to see what it was, gave them my sexual history, and told them that there was a good chance I did have AIDS.  They biopsied it, and the diagnosis was Kaposi’s sarcoma. That was March 8.

Obviously, the first day I was very, very upset, and I went into a deep depression for about a month.  I came home that night and my significant other held me in his arms, and I said to him, “Why do I feel like Ali McGraw, it is just like a movie, it is really terrible, it is the most horrible thing that ever happened.”

My depression lasted a month, and I decided if there was any chance I was going to get over this, if I had any chance of surviving at all, I would have to have a more positive attitude and just continue on, live my life as best I can, and try not to worry about it too much.

I was very lucky. I had the choice of being treated at GW by a very good cancer specialist there, who instilled a great deal of confidence in me, or I had the choice of being treated at the National Institutes of Health.

I think it was an easy choice, because I think — NIH wanted me, because I was so healthy at that point.  I was a good specimen for research I think.  And also, I felt that if I have the disease and no one knows anything about it, the best place to be treated would be where they are doing the research.

* * * * * *


December 5, 1983
San Francisco Chronicle Exposes Delay in AIDS Funding

Reporter Randy Shilts of the San Francisco Chronicle writes that federal health officials were forced to pull funding from other projects to support important AIDS research in the spring of 1983 due to the lack of federal funding.

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Top officials in the Department of Health and Human Services were pleading for more federal funds from the Reagan administration for AIDS research in early 1983, all while publicly saying that no more money was needed, according to Shilts’ reporting in The Chronicle.

Reporting from documents obtained under the Freedom of Information Act, Shilts wrote that the Centers for Disease Control in Atlanta ultimately were forced to divert millions of dollars from other important health projects in order to conduct AIDS research.

Dr. James Curran, director of AIDS research at the Atlanta center, said 2,513 cases had been reported to the CDC as of Oct. 17, 1983, and 1,048 people had died, reflecting a fatality rate of 41%.
“It has now reached the point where important AIDS work cannot be undertaken because of the lack of available resources,” wrote Edward Brandt, assistant secretary of the Department of Health and Human Services, in a May 13, 1983 memo.

In that memo obtained by Shilts, Brandt listed a number of important health areas other than AIDS in which work was “postponed, delayed or severely curtailed” because the center was diverting money to AIDS research.

But according to The Chronicle, Brandt also publicly supported the Reagan administration’s position just days before, testifying May 9 to Congress that extra funds to fight AIDS were “unnecessary.”

Dr. William Foege of the Centers of Disease Control sent Brandt a 12-page request for funds in early May, but two weeks later, Thomas Donnelly, Assistant Secretary for Legislation, wrote a Senate staff member that “we are not in favor of additional appropriations” for AIDS research.  The Office of the Assistant Secretary for Legislation serves as the primary link between the Department of Health and Human Services and Congress.

March 6, 1984
Blood Supply Task Force Opposes Test for Screening Virus

The task force created at the December 1983 FDA/CDC conference with the blood services community issues a report with a majority opinion that opposes the implementation of incorporating hepatitis B anti-core testing into the routine screening of plasma, presenting another roadblock to the protection of the country’s blood supply.

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The task force reviewed several pilot tests performed at blood banks in areas with donors at high risk for hepatitis B core antibody (anti-HBc), which appears at the onset of symptoms in acute hepatitis B and persists for life.  Scientific data suggested that anti-HBc was found commonly in HIV-infected individuals.

Data showed:

  • 5-18% of blood and plasma donors had a positive test for anti-HBc;
  • 84% of homosexual males tested positive for anti-HBc; and
  • 96% of IV drug users tested positive for anti-HBc.

The discussion at the December BPAC meeting had stipulated that ”cost-benefit analysis and disease prevalence must be considered in the decision regarding whether or not to use the test,”  However, the task force could not agree upon the true cost of the test, with estimates as low as $2.50 per test for plasma collectors and as high as $12.00 per donation for whole blood collections

Additional costs were the blood that would be discarded and the recruitment of new donors.  With the task force unable to agree on the costs and the benefits of using the anti-core test as a surrogate for high-risk donors, the majority decided to oppose the adoption of screening procedures.

April 5, 1985
Atlanta Hosts International AIDS Conference

The U.S. Department of Health and Human Services and the World Health Organization  host the first International AIDS Conference  in Atlanta, Georgia on April 15-17.

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More than 2,000 researchers gathered at the conference to share information and assess prospects for controlling the disease, not yet realizing that the worst was yet to come.

The Atlanta conference featured 392 presentations and generated considerable excitement among participants eager to learn about how this new disease was playing out within specific populations in the U.S.

Much of the news was discouraging, however, as presenters introduced new data that showed that many of those dying in 1985 had been infected before 1981, and that within especially vulnerable populations, the epidemic was becoming entrenched.

At a side meeting before the day the conference opened, gay activists protested Reagan administration proposals to implement mandatory HIV testing policies, arguing that this would do little to halt the spread of the disease and would only intensify discrimination against vulnerable groups.

August 31, 1985
Pentagon Announces Testing of Military Recruits

The Pentagon announces that, beginning October 1, it will begin testing all new military recruits for HIV infection  and will reject those who test positive for the virus.

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Two Pentagon officials, who spoke to The New York Times on the condition they not be identified, said the new directive was promoted most vigorously by top Army officials, out of concern about the potential high cost of treating soldiers who are found to have the disease. Pentagon officials said about 50 soldiers are being treated in military hospitals for the disease.

The U.S. military does not universally test potential recruits for any other disease or disorder as a condition of enlistment, although new recruits are usually tested for syphillis and German measles soon after they enlist.

The announcement was condemned by the Lambda Legal Defense and Education Fund, which asserted that the testing would unfairly stigmatize many people who have been exposed to the virus but who do not have the disease.

Timothy Sweeney, executive director of Lambda Legal, also contended that military testing for HIV might become a precedent for AIDS screening in private industry.

September 17, 1985
Reagan Finally Mentions ‘AIDS’ in Public Remarks

President Ronald Reagan mentions AIDS publicly for the first time, calling it “a top priority” and fending off criticism that funding for AIDS research is inadequate.

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By the end of 1984, AIDS had already ravaged the United States for a few years, affecting at least 7,700 people and killing more than 3,500. Scientists had identified the virus that caused AIDS and the U.S. Centers for Disease Control and Prevention (CDC) identified all of its major transmission routes.

This is why it is notable that it took until September 1985, four years after the crisis began, for Reagan to first publicly address the subject of AIDS.

Exchanges between the Reagan administration and journalists in the early 1980s demonstrate that Reagan and his staffers didn’t take the epidemic very seriously, for which the Reagan administration is still heavily criticized.

Reagan’s successors in the White House eventually acted, albeit often very slowly, on the crisis — leading to much more research, programs like the Ryan White CARE Act that connect people to care, and the development of antiretroviral medication that increases the life expectancy of a person living with HIV by decades.


October 2, 1985
Congress Allocates $190M for AIDS Research

 Congress allocates nearly $190 million for AIDS research — an increase of $70 million over the Reagan Administration’s budget request.

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The House Appropriations Committee also urges President Reagan to appoint a coordinator for the AIDS effort, “in other words, an AIDS czar.”

“Nine agencies have been engaged in this effort. … What we need is a well-coordinated, well-planned effort, with one person running the show,” said Rep. Silvio Conte, (Mass), the senior Republican on the House Appropriations Committee.

The National Institutes of Health would receive $140.6 million, the Centers for Disease Control would receive $45.6 milion and $3.5 million would go to the Alcohol, Drug Abuse and Mental Health Administration.

During debate on the appropriations bill, the House accepted an amendment by Rep. Robert Dornan (R-Calif.), that would allow the surgeon general to use some funds to close bath houses “that may be responsible for transmitting AIDS.”

New City of West Hollywood Launches AIDS Response

About one year after West Hollywood is officially incorporated as an independent city, it begins actively addressing the HIV/AIDS epidemic.

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HIV/AIDS had a significant impact on the City of West Hollywood due to the disease’s elevated infection rate among gay men, which caused a devastatingly high number of deaths among the city’s population.

Following the City of West Hollywood’s incorporation as a city on November 29, 1984, elected officials and city staff begin working on a plan to address the epidemic in their own backyard.

In October 1985, the city launches an AIDS awareness campaign, one of the first in the country.  The City of West Hollywood also becomes one of the first government entities to create a program for awarding social services grants to local HIV/AIDS organizations.  The city’s response to the AIDS crisis would go on to be recognized as a model for other cities, nationally and globally.

Also during its first year of cityhood, West Hollywood would adopt landmark legislation to establish rent control and prohibit the discrimination against people with HIV and AIDS.  Today, many of the city’s landmark ordinances have been duplicated and have become mainstream policies nationally and globally.

October 25, 1985
NY Moves to Close Gay Bars & Bathhouses

The New York State Public Health Council empowers local health officials to close gay bathhouses, bars, clubs , and other places where “high-risk sexual activity takes place.”

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The Public Health Council resolution went beyond recommendations made by Gov. Mario M. Cuomo and State Health Commissioner David Axelrod by defining “high-risk sexual activity” to include oral sex.

Mayor Edward I. Koch announced that the new regulation takes effect immediately and is to be enforced by NYC Health Department inspectors who will enter bathhouses in uniform and undercover.

The National Gay Task Force opposes the regulation, citing discriminatory practices.

“This appears to be an unequal application of law” because many experts say AIDS can be transmitted by heterosexual activity, said Ron Najman, a spokesman for the National Gay Task Force. “They are concentrating on the homosexual aspect.”


December 4, 1985
LA County Imposes Regulations on Bathhouses

Los Angeles County enacts strict regulations on local bathhouses to stop the spread of HIV, and bathhouse owners file suit to stop the regulations from going into effect.

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The LA County Board of Supervisors introduced new county regulations that could put patrols inside bathhouses to ensure that patrons don’t participate in sex acts considered to be unsafe.

“If someone showed me data substantiating a correlation of the spread of this disease and my club, I would deliver the keys to City Hall tomorrow. But so far it’s only been speculation, hysteria and panic, ” Silver Lake bath house owner Steve Downard told the Los Angeles Times.

“The sexual activity at the club is the same as at the Biltmore Hotel, but there are no health posters, no monthly health screening and no free condoms at the Biltmore.”

Under the new County rules, unsafe sex is defined as anal and oral intercourse between men, with or without a condom. Clubs with repeated violations could face closure.

The fact that the county rules make no mention of heterosexual acts, which also can spread AIDS, is proof, Downard says, that homophobia, not health concerns, are behind the regulations.

December 13, 1985
France Sues U.S. for Credit for Discovery of AIDS Virus

The Pasteur Institute files a suit against the U.S. Government in the U.S. Court of Claims in Washington, DC., seeking recognition that French researchers were the first to discover the virus that causes AIDS.

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The long-simmering transatlantic feud over who will receive royalties on a test for the AIDS virus has erupted into a legal battle, with French scientists seeking recognition in the U.S. courts for their claim that they discovered the virus before their American counterparts.

The Pasteur Institute ‘s suit also seeks the right to grant permission to sell the blood test without being sued by the U.S. for counterfeiting, and the right to share in royalties collected by the U.S. for sales of blood tests by U.S. licensees.

The French scientists were the first to publish a paper on the virus, said Dr. Robert C. Gallo, the U.S. scientist credited with discovering HIV. But he asserts in an interview with the Los Angeles Times, “I was the first to suggest it was a retrovirus.”

“We had this virus in 1982. We didn’t publish on purpose because we didn’t understand it well enough to stick our necks out. To me, ‘discovery’ is a complicated word. Who first reported discovery of a virus?  They did.  But if the idea comes first — that was us.”

In July 1994, U.S. health officials would concede for the first time that American researchers used a virus obtained from French competitors to make the first American AIDS test kit. At that time, the U.S. would announce the signing of an agreement that would give the French a bigger share of royalties from worldwide sales of AIDS tests.

The contract would end the long-standing and sometimes acrimonious dispute that strained relations between the two countries.


June 30, 1986
U.S. Supreme Court Upholds Georgia Sodomy Law

Bowers v. Hardwick was a landmark decision of the U.S. Supreme Court that upheld, in a 5–4 ruling, the constitutionality of a Georgia sodomy law criminalizing oral and anal sex in private between consenting adults.

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The majority opinion, by Justice Byron White, reasoned that the Constitution did not confer “a fundamental right to engage in homosexual sodomy.”  A concurring opinion by Chief Justice Warren E. Burger cited the “ancient roots” of prohibitions against homosexual sex, quoting William Blackstone’s description of homosexual sex as an “infamous crime against nature,” worse than rape, and “a crime not fit to be named.”

The case arose on August 3, 1982, when a police officer who had been admitted to the home of Michael Hardwick in Atlanta witnessed him and a male companion in a bedroom engaging in sex.  The officer had been executing a warrant for Hardwick’s arrest for failing to appear in court on a charge of public drinking (it was later determined that the warrant was invalid because Hardwick had already paid the $50 fine).  The officer promptly arrested both men for violating Georgia’s antisodomy statute.

In its decision, the Court ruled that while the “right to privacy” protects intimate aspects of marriage, procreation, contraception, family relationships, and child rearing from state interference, it does not protect gay sodomy because “no connection between family, marriage, or procreation on the one hand and homosexual activity on the other has been demonstrated.”

The Supreme Court decision would stand for 17 years until 2003, when Lawrence v. Texas would overturn Bowers.

Roy Cohn (2)
August 2, 1986
Notorious Lawyer Roy Cohn Dies

Roy Cohn, best known for his role as chief counsel to Sen. Joseph McCarthy in the 1950s investigation of alleged Communist sympathizers, dies of AIDS-related illness at the age of 59.

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A graduate of Columbia Law School at the age of 20, Cohn quickly made a name for himself in his first job with the U.S. attorney’s office in Manhattan, prosecuting cases of people with alleged ties to the Communist Party.

Impressed with Cohn’s performance at the trial of Julius and Ethel Rosenberg for spying, FBI director J. Edgar Hoover would recommend that Cohn be hired as chief counsel to the Senate Permanent Subcommittee on Investigations. McCarthy, who chaired the panel, hired the 24-year-old Cohn in January 1953.

“People born in the 1940s or earlier remember Cohn and his master performing on television,” writes Mary Ellen Clark in her 1988 book The Snarling Death of Roy M. Cohn.  “They remember coming home to be hushed by a mother or aunt who was watching the hearings; they remember a father’s opinion, expressed at the family table when families still ate together.”

“For younger people, however, Roy Cohn was simply another name for a très smart lawyer, for Disco Dan, for the international, I-go-by-private-plane man,” writes Clark.

Throughout his later life, Cohn was well known for his lavish Washington parties, with wealthy and famous friends among his guests.

“He was a figure very tough and in on things, a champion of the underdog, though definitely running with the overdog pack,” Clark writes.  “He nested on the nighttime radio call-in shows; he spread his wings over Koppel on Nightline.  He appeared to be able to avoid all taxes and all penalties, maybe because he was connected, or on the A list, or known to the headwaiters and hostesses of New York.”

Cohn would be indicted four times from the mid-’60s to the early ’70s — for stock-swindling, obstructing justice, perjury, bribery, conspiracy, extortion, blackmail, and filing false reports.  He is acquitted in three of the cases, and in the fourth, he would escape with a mistrial.  This experience would give him “a kind of sneering, sinister sheen of invulnerability,” writes Michael Kruse in Politico.

Cohn would be diagnosed with HIV in 1984 after having a doctor examine a small cut from shaving that wouldn’t stop bleeding.  During the visit, the doctor would re­move two suspicious growths and the tests would reveal Cohn is HIV positive.

Cohn’s lover Peter Fraser, a New Zealander roughly half Cohn’s age, reported that, “When he found out, he didn’t cry but a couple of tears.”

Cohn would publicly deny that he was HIV positive and would keep his sexuality closeted for the rest of his life.  According to Robert E. Bauman, who says he first meets Cohn on the day McCarthy dies in 1957, Cohn paradoxically had a reputation for “fag bashing” and loudly opposed laws that protected gays from discrimination.

In his last months of life, Cohn would be disbarred from law practice in New York for old fraud charges and he would lash out at the bar ethics committee, calling members “a bunch of yoyos.”

Cohn once said he wanted the first line of his obituary to read: “Roy M. Cohn, who served as chief counsel to Sen. Joseph R. McCarthy.”

“Cohn didn’t quite get his wish,” writes Bauman.

When Cohn dies, the headlines would trumpet the fact that he died from complications of AIDS.  The mention about McCarthy would come second.

October 9, 1986
Violence Against Gays and Lesbians on the Rise

One in every five gay men and one in every 10
lesbians report being physically assaulted because of their sexual orientation, according to an eight-city study of antigay violence conducted by the National Gay and Lesbian Task Force.

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In the first Congressional hearing to address anti-gay violence, Kevin Berrill of the National Gay and Lesbian Task Force (now called the National LGBTQ Task Force) told members of the House Subcommittee on Criminal Justice that in addition to battling the AIDS epidemic, the gay community was also contending with rampant and deadly antigay violence.

“There is disturbing evidence that the AIDS and antigay violence epidemics may now be following the same menacing curve,” Berrill said.  “For inasmuch as AIDS has spread, so has the fear and hatred that spawns violence.”

Berrill went on to criticize the federal government for viewing widespread violence against gay men and lesbians as “just a gay problem and therefore not of concern to all society.”  He bitingly referred to this passive policy as the same one the government has adopted to address HIV and AIDS.

In its study on antigay violence, the Task Force surveyed more than 2,000 community members in eight cities.  Berrill also presented data from local governments which confirmed the Task Force’s findings.  At the time, the federal government did not collect data on violence against LGBTQ community members.

“The toll of antigay violence cannot be measured solely in terms of these statistics,” Berrill told the Congress members.  “These numbers do not measure the anguish, fear and loss experienced by Dee, who is still recovering from burns caused by acid thrown at her face when she was leaving the Los Angeles Gay Community Center.  Or by Robert from New Jersey, where assailants beat him, extinguished cigarettes in his face, and then tied him to the back of a truck, dragging him in tow.  Or by the family and friends of Charlie Howard of Maine, who was thrown off a bridge to his death by three teenagers.”

Berrill called on Congress to initiate federal studies on antigay violence and pass tougher laws to combat violent crimes targetting gays and lesbians.  He also urged the repeal of all sodomy laws (which were still on the books of most states), and called for the passage of legislation prohibiting discrimination on the basis of sexual orientation.

Also testifying that day was Diana Christensen, executive director of the Community
United Against Violence in San Francisco, who told the subcommittee the following:

“Is the increase in antigay violence an indicator of an AIDS-related backlash?  At this point, I believe that AIDS and homosexuality have become synonymous in the American public’s mind.  For the homophobic mind, AIDS is simply another justification for violence.”

David Wertheimer, executive director of the New York City Gay and Lesbian Anti-Violence Project (which would become the NYC Anti-Violence Project) also provided the highlights of his 20-page testimonial submitted to the subcommittee.  Founded in 1980 to provide support services to lesbian and gay survivors of homophobic violence, the organization became a city-wide, nonprofit service
provider in 1983.

Wertheimer reported that between 1984 and 1985, reported cases of violence “began to mushroom,” and the organization’s caseload increased 41%.  In the current year — 1986 — violence was reported even more frequently, with between 40 and 60 new cases each month.

He explained that in the past, cases typically were in the form of antigay and antilesbian verbal harassment in a public place, or in the form of menacing behavior or even assault.  A new form of violence had emerged recently, Wertheimer said, one that now represented 28% of the Anti-Violence Project’s caseload.

“AIDS-related violence — that is violence that may begin with verbal and menacing acts that are specifically related to AIDS,” he said.  “For example, someone might start an attack by saying, ‘I hate faggots. You faggots give us AIDS.’  Or a lesbian might find notes on her door saying ‘Lesbians, dykes, you give us AIDS. Get out of the building.'”

Wertheimer told the Congress members that antigay violence can result in death.  The organization reported seven antigay homicides in 1985, and 15 such homicides in the first nine months of 1986.

Also providing testimony was Dr. Gregory M. Herek, assistant professor of psychology at
the City University of New York and a member of the American Psychological Association’s Committee on Lesbian and Gay Concerns.

“A growing body of scientific data, including my own empirical research, shows that individuals’ irrational fears surrounding AIDS — such as fear of transmission through casual contact — are highly
correlated with their level of homophobia,” Dr. Herek said.  “I interpret this finding to mean that reducing AIDS hysteria requires confronting its roots in homophobia, and that eliminating homophobia will require education about AIDS. Unfortunately, the U.S. Justice Department has sanctioned discrimination based on fears of AIDS-contagion, and has thereby fueled fears about AIDS
and probably contributed to public homophobia.”

Rep. Barney Frank (who in 1987 would become the first member of Congress to be openly gay) also spoke for the Congressional record in support of raising awareness about anti-gay violence.



U.S. Grant Program Feeds Growing Healthcare Needs

The U.S. launches the AIDS Service Demonstration Grants program, allocating $15.3 million in available funding to New York, Los Angeles, San Francisco and Miami.

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The grant program is run by the Health Resources and Services Administration, an agency of the U.S. Department of Health and Human Services.  As the HRSA’s first AIDS-specific health initiative, program focused its funding on cities hardest-hit by HIV/AIDS.

In the years to come, the HRSA would create the HIV/AIDS Bureau and develop a comprehensive system of HIV primary medical care, medications, and essential support services for low-income people with HIV.

The HIV/AIDS Bureau will oversee the Ryan White HIV/AIDS Program and play a critical role in helping diagnose, treat, prevent, and respond as part of the “Ending the HIV Epidemic: A Plan for America” initiative.

Koop report (2)
October 22, 1986
Surgeon General Releases Report on AIDS

The Surgeon General issues the Surgeon General’s Report on AIDS. The report makes it clear that HIV cannot be spread casually.

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The report, issued by U.S. Surgeon General C. Everett Koop, M.D., also calls for a nationwide education campaign that includes early sex education in schools, increased use of condoms, and voluntary HIV testing.

“By the end of 1991, an estimated 270,000 cases of AIDS will have occurred with 179,000 deaths within the decade since the disease was first recognized,” Dr. Koop states in the report’s preface.

“In the year 1991, an estimated 145,000 patients with AIDS will need health and supportive services at a total cost of between $8 and $16 billion.”

October 29, 1986
Report Calls for Nationwide Education Campaign

The National Academy of Sciences issues a report calling for a “massive media, educational and public health campaign to curb the spread of the HIV infection,” as well as for the creation of a National Commission on AIDS.

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The report, titled  Confronting AIDS: Directions for Public Health, Health Care, and Research,  is issued by  the Institute of Medicine (IOM), the principal health unit of the NAS.  The IOM anticipates that the cost of the public health campaign will reach $2 billion by 1990.

The mission of NAS is to provide scientific advice to the government “whenever called upon” by any government department. The Academy receives no compensation from the government for its services.

February 1, 1987
Global Response Begins with WHO Program

The World Health Organization (WHO) launches the Special Programme on AIDS to serve as the architect and keystone of a global AIDS plan.

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The mission set out by the Special Programme was to:

  • raise awareness;
  • formulate evidence-based policies;
  • provide technical and financial support to countries;
  • initiate relevant social, behavioral, and biomedical research;
  • promote participation by nongovernmental organizations; and
  • champion rights of those living with HIV.

With the technical and financial support of the Special Programme, AIDS programs rapidly begin to be established in nations throughout the world.  The program recogizes that AIDS affects both the developing and the industrialized worlds; and, therefore, every country will need a national AIDS program.

WHO puts forth the idea that a global response is vital not only for national interests but also because “ultimately AIDS cannot be stopped in any one country unless it is stopped in all countries.”

At the global level, the Special Programme is responsible for strategic leadership, developing consensus, coordinating scientific research, exchanging information, assuring technical cooperation and mobilizing and coordinating resources. By the end of 1988, the Special Programme would support every country in the world that requests collaboration.

In 1988, it will be renamed the Global Programme on AIDS.

March 19, 1987
U.S. Approves AZT, First Medication for AIDS

The Food and Drug Administration (FDA) approves the first medication for AIDS — AZT (zidovudine), an antiretroviral drug initially developed to treat cancer.

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FDA directors approved AZT treatment, even though they had serious concerns about the toxicity of the medication.

As the only medication available to treat HIV, AZT became a highly sought-after treatment, albeit one fraught with side effects.  Studies showed that AZT therapy could lead to the damage of muscle tissues, including the heart, and also the suppression of the production of red blood cells, neutrophils, and other cells in the bone marrow.

In addition, the side effects of fatigue, malaise, and anemia were common.  Many patients taking AZT experienced gastrointestinal intolerance, nausea and vomiting.  Rarer side effects included lactic acidosis and hepatic steatosis.

The drug’s approval remains controversial to this day, but now that we are in a world where treatment options are so far advanced, it can be difficult to imagine the sense of urgency permeating the medical community in the 1980s.

Today, if someone is diagnosed with HIV, he or she can choose among more than 40 drugs that can treat the disease. And there is an excellent chance that with the right combination of medications, given at the right time, HIV levels can be reduced and kept so low that the person never gets sick and the virus becomes undetectable.

March 24, 1987
FDA Accelerates Drug Approvals

The U.S. Food and Drug Administration issues regulations that expand access to promising new medications that have not yet been approved or licensed by the agency. This accelerates the approval of drugs by two to three years.

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In a few months, the FDA would go on to issue treatment IND (investigational new drug) regulations on May 22 to permit new drugs to be used to treat patients before clinical trials are completed where no alternative therapy exists for a “serious disease.”

In its explanation of the regulations, the FDA mentions advanced cases of AIDS as the first example of an immediately life-threatening disease, but did not include AIDS in its list of examples of serious diseases.  It explained that some diseases, like multiple sclerosis, are not serious at earlier stages, and that the Treatment IND regulations would not apply to drugs intended to treat those earlier stages of disease.

March 31, 1987
American & French Researchers Share Credit for Discovery of Virus

President Ronald Reagan and French Prime Minister Jacques Chirac end an international scientific dispute when they announce that researchers from the two countries will share credit for discovery of the AIDS virus.

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The countries agree that patent rights to a blood test that emerged from that discovery will also be shared, with most of the royalties to be donated to a new foundation for AIDS research and education.

This settles a years-long rift between the two countries, each laying claim to the valuable patent for the first HIV-antibody test.  The U.S. Department of Health and Human Services claimed virologist Robert Gallo first developed the test, while the Pasteur Institute claimed it was French virologist Luc Montagnier.

Gallo had won the prestigious Lasker Award in 1986 for his share of the work (his second Lasker, having won in 1982 for his work on retroviruses).

Years later, the National Institutes of Health would conduct an investigation that proves Gallo and his colleagues first had isolates of HIV with the exception of one sample that originated from the Pasteur Institute’s lab (which was requested by the Gallo lab and sent to them from Paris).

Gallo and Montagnier later agree to share the title of co-discovers of the virus and they write several papers together describing their work in Science (Dec. 29, 2002) and the New England Journal of Medicine (Dec. 11, 2003).

However, in 2008 when Stockholm would call with the Nobel Prize for Physiology or Medicine, it was only for Luc Montagnier.  The scientific world would be shocked to learn that the Nobel Committee was snubbing Gallo’s work, but because those archival records are locked up until 2058, we will not know the precise argument behind this decision for many years.

April 6, 1987
Dr. Koop Focuses on Children with AIDS, Calls for Sex Ed

At a four-day workshop at Children’s Hospital of Philadelphia, U.S. Surgeon General C. Everett Koop draws attention to the plight of the growing number of children who acquire AIDS from their mothers or through blood transfusions.

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The workshop kicks off with a large press conference, where Dr. Koop announces that AIDS is a growing menace to the nation’s children and reiterates his call for early sex education as part of the general effort to halt its spread.  He recommends that sex education start in kindergarten and include information about AIDS.

”It’s the responsibility of parents, and it should begin before children go to school,” Dr. Koop says.

He mentions that parents are often reluctant to discuss sex with their children, and so the burden falls upon schools, churches and synagogues to teach children and youth about sex and AIDS.

“If parents don’t do it, they’ve abrogated their responsibility and somebody else has to do it,” Dr. Koop says.

Dr. Koop’s stance for early sex education puts him at odds with some of his fellow conservatives.

The workshop brings together families affected by HIV, leading HIV researchers and clinicians, mental health professionals, public health officials, and representatives from the insurance, legal, and nonprofit organizations.

In the last week, the number of children under 13 years old diagnosed with AIDS reaches 471, double the number of cases reported a year ago, according to the Centers for Disease Control. In addition, there are 139 cases among teen-agers.

But Dr. Koop says these figures do not include as many as 2,000 children who have some AIDS symptoms but who do not meet the strict Federal definition of the illness, and he says the number of infected children is expected to continue to increase ”dramatically.”

Dr. Koop also notes that a disproportinate number of children infected with AIDS are members of minority groups: about 50% are black and 33% are Hispanic.

”We have, therefore, a segment of society that is very difficult to reach,” Dr. Koop says.

gold condom
April 7, 1987
FDA Declares HIV Prevention as Indication for Condoms

The U.S. Food and Drug Administration authorizes the sale of male condoms to include HIV prevention as an indication for use, marking a major stride in public health communication and safe sex and HIV/AIDS transmission.

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AIDS brings condoms back to the forefront for sexually active people of all sexual orientation.

Nevertheless, condom use does not equal 100% protection from HIV, and its effectiveness largely depends on correct and consistent use.  Also, some people are allergic to the latex, lubricants, and perfumes.

The FDA also begins to test latex condoms for leaks, resulting in an improvement in the overall  quality of condom products.

May 15, 1987
U.S. Bans HIV-Positive Immigrants & Travellers

The U.S. Public Health Service adds HIV as a “dangerous contagious disease” to its immigration and travel exclusion list. The HIV ban will not be lifted until 2010.

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“It was not the discovery of HIV alone, but the economic and political climate of the 1980s that led to the introduction of the ban,” writes Dr. Susanna E. Winston and Dr. Curt G. Beckwith in AIDS Patient Care STDS.

In the early 1980s, a worldwide economic recession drove immigrants to enter the U.S., fueling American fears of foreigners taking jobs and becoming a burden on the health and welfare systems.  This coincided with the explosion of the AIDS epidemic, with fear and misunderstanding about the disease feeding into the growing xenophobia.

It is in this environment that HIV/AIDS is added to the U.S. list of dangerous contagious diseases.

At first, only individuals whose illness advanced to AIDS are excluded from U.S. travel (based on the argument that AIDS affects a person’s wage-earning capacity). But then, under pressure to demonstrate efforts to combat the HIV/AIDS epidemic, President Reagan moves to require all immigrants be tested for HIV, and that HIV infection (with or without AIDS) be included as a disease of public health significance.

This adds HIV to the list of dangerous diseases that includes leprosy, tuberculosis, syphilis and gonorrhea.

The U.S. starts mandatory AIDS testing of the 500,000 applicants seeking permanent residence.  The ban includes travellers from other countries who test positive for HIV.

The ramifications of the HIV immigration and travel ban would come to light both domestically and internationally with the case of Hans Paul Verhoef.  While traveling to San Francisco to attend the 1989 National AIDS Forum, Verhoef, an HIV-infected Dutch citizen and rising chair of the Dutch HIV Foundation, would be detained and arrested when Immigration and Naturalization Service agents find AZT in his luggage.

Verhoef’s arrest sets off an outcry from the international AIDS community in objection of the ban, with protests and threats of boycotts of the two upcoming international conferences, planned for San Francisco (1990) and Boston (1992).  For the 1990 International AIDS Conference (IAS), President George H.W. Bush issues an executive order temporarily waiving the ban for all attendees.  But IAS organizers decide to hold no further conferences in the U.S. until the ban is revoked, and the 1992 IAS conference is relocated from Boston to Berlin.

The travel ad immigration ban would be lifted 22 years later, on January 4, 2010.  A new federal rule under President Barack Obama’s administration would be heralded as a monumental achievement, accomplished through the hard work of advocates.


May 31, 1987
President Reagan Makes His First Public Speech about AIDS

President Ronald Reagan makes his first public speech about AIDS at the American Foundation for AIDS Research Awards Dinner.

The epidemic is now six years old; 36,058 people have been diagnosed with the disease and 20,849 have died.

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amFAR event attendees “boo” Reagan when he says he asked the Department of Health and Human Services “to add the AIDS virus to the list of contagious diseases for which immigrants and aliens seeking permanent residence in the United States can be denied entry.”

Attendees also shout out their opposition when the president says he is ordering testing for active members of the military, those seeking care at veterans’ hospitals, applicants for marriage licenses, and federal prisoners.

Among the event attendees are amfAR Founder and National Chairperson Elizabeth Taylor and amfAR President Dr. Mervyn Silverman.

After Reagan speaks, Taylor tries to move ruffled feathers by telling the audience, “While there are differences of opinion on AIDS testing,” Reagan’s remarks are ”basically in concurrence with what we all hope and pray for,” namely a cure for the disease.

AmfAR advocates for voluntary, confidential testing accompanied by intense counseling, adds Dr. Silverman.

After the event, U.S. Surgeon General Dr. C. Everett Koop said he ”found no fault with the speech” and that he considered it reasonable to test Federal prisoners and immigrants and to offer the test to marriage applicants.  He also said he was embarrassed by the reaction of some in the audience.

“I never heard anyone boo the President before,” Dr. Koop said.

June 24, 1987
President Reagan Creates Commission on AIDS

President Reagan signs an Executive Order creating the first Presidential Commission on AIDS.

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Two days later, Reagan would appoint Dr. W. Eugene Mayberry, CEO of the Mayo Clinic, to chair the commission.  Jeff Levi, executive director of the National Gay and Lesbian Task Force would object to the appointment of someone with no experience with the disease, but others praise Mayberry’s experience in both medical research and clinical services.

The president also appointed the following people to the Commission:

  • Dr. Colleen Conway-Welch, dean of nursing at Vanderbilt University
  • John J. Creedon, CEO of Metropolitan Life Insurance Company
  • Dr. Theresa L. Crenshaw, a sex educator and opponent of condoms as a means of preventing the spread of HIV
  • Richard M. DeVos, president of Amway
  • Dr. Burton J. Lee III, a physician at the Memorial Sloan-Kettering Cancer Center
  • Dr. Frank Lilly, a geneticist at the Albert Einstein College of Medicine. Lilly served on the board of the Gay Men’s Health Crisis, and is “one of the first openly gay Presidential appointees”
  • Dr. Woodrow A. Myers Jr., an African American, the health commissioner of Indiana, and president of the Association of State and Territorial Health Officers
  • Cardinal John O’Connor, an opponant of including instruction about condoms in AIDS education programs in schools
  • Penny Pullen, an Illinois legislator. advocate of mandatory premarital HIV testing who would go on to found the conservative Christian organization Illinois Family Institute
  • Corinna “Cory” SerVaas, editor of the Saturday Evening Post
  • Dr. William B. Walsh, president of Project HOPE, a medical relief organization
  • James D. Watkins, a retired admiral

Dr. Lilly of the GMHC is considered to be the most controversial appointment, opposed by conservaties including Sen. Gordon Humphrey (R-New Hampshire).

“The President should strive at all costs to avoid sending the message to society – especially to impressionable youth – that homosexuality is simply an alternative lifestyle,” Sen. Humphrey tells The New York Times.

At the commission’s first meeting, Lilly finds himself seated next to Cardinal O’Connor, and they would be observed “chatting cordially.”

August 5, 1987
Florida Schools Ordered to Enroll HIV-Positive Brothers

A federal judge orders the DeSoto County School Board in Florida to enroll HIV-positive brothers Ricky, Robert, and Randy Ray.  The school board had refused to allow the three boys to attend the district’s schools in their hometown of Arcadia, Florida.

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After the court ruling, some town residents would refuse to allow their children to attend school, many would anonymously call the Ray home with threatening messages, and ultimately someone would set fire to the Ray house, destroying it and forcing them to move.

“Arcadia is no longer our home,” their father, Clifford Ray, tells the press the day after the fire. “That much was made clear to us last night.”

Ricky, Robert and Randy, who were 10, 9 and 8 at the time, were all born with hemophilia, a condition that required them to receive blood transfusions.  Ricky would go on to become an activist in the fight against AIDS.  President Bill Clinton reaches out to him and thanks him for his work raising awareness about HIV/AIDS.

The young teenager would allow camera crews to document his declining health, saying he wanted  Americans to see what AIDS did to people.  Ricky Ray would die in 1992 at age 15.

Robert would die of AIDS-related causes in 2000 at the age of 22.  Shortly thereafter, their father would attempt suicide but would survive.  Randy Ray would marry in 2001 and settle in Orlando, Florida, successfully managing his HIV through medication.

August 18, 1987
Human Testing of HIV Vaccine Begins

FDA sanctions the first human testing of a candidate vaccine against HIV.  While the clinical trials do not lead to a vaccine, the FDA’s approval marks an important milestone in the development of HIV/AIDS treatment options.

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Manufactured by MicroGeneSys of West Haven, Conn., the vaccine would move forward to clinical trials supervised by the National Institute of Allergy and Infectious Diseases.  Just months ago, NIAID Director Dr. Anthony Fauci said that the FDA was considering several candidate vaccines and that human trials could begin in 1987.

In early 1993, MicroGeneSys would pull the vaccine, called VaxSyn, from National Institutes of Health trials because the pharmaceutical company could not agree with the NIH over the dosing schedule. The vaccine has already been selected for inclusion in a $20 million U.S. army trial program.

Today, there is no vaccine available to prevent HIV infection or treat those who have it.

However, scientists are still working to develop one. NIH is investing in multiple approaches to prevent HIV, including a safe and effective preventive HIV vaccine. These research efforts include two late-stage, multinational vaccine clinical trials called Imbokodo and Mosaico.


October 9, 1987
UK Prime Minister Thatcher Gives Anti-Gay Speech at Convention

Margaret Thatcher, prime minister of the United Kingdom, sums up her party’s dark views toward the LGBT community in an anti-gay speech, garnering her thundrous applaus at the 1987 Conservative Party conference.

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From her convention podium, Thatcher declared:  “Children who need to be taught to respect traditional moral values are being taught that they have an inalienable right to be gay, ” she said.  “All of those children are being cheated of a sound start in life. Yes, cheated.”

In less than a year later, Thatcher would usher in the passage of Clause 28, anti-gay legislation to stop all discussion of homosexuality in British schools.   An amendment to the 1988 Local Government Act, Section 28 would effectively ban local authorities and schools from “promoting” homosexuality.  Government funds could no longer go toward of books, plays, leaflets, films, or other materials showing same-sex relationships, while teachers weren’t allowed to teach about gay relationships in schools.

In the shadow of the AIDS epidemic, the United Kingdom in the 1980s was a place of renewed LGBT activism and a forward movement toward equal rights.  New progressive legislation opened the door for the Greater London Council to fund LGBT groups, and some local authorities in London and Manchester began to employ officers to counter homophobia.

There were also alliances between LGBT organizations and labor unions, such as the one between the mineworkers union and a lesbian-gay support group.   And in 1985, Margaret Roff became the mayor of Manchester, making her the first openly lesbian woman to hold such a post in the UK.

But all this progress was made while the UK media was using the outbreak of AIDS/HIV to demonize gay and bisexual men.  Thatcher and her Conservative Party saw this as an opportunity to activate their base and even win some votes from “the Labour left.”

At the start of her third term as prime minister, Thatcher gave the speech that made her intentions clear, in front of the audience she knew would praise her pronouncements.

leather man
October 11, 1987
Helms Amendment Imposes Restrictions on AIDS Education

In a 94-2 vote, the U.S. Senate adopts the Helms Amendment, which requires federally financed educational materials about AIDS to stress sexual abstinence and forbids any material that “promotes” homosexuality or drug use.

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The Helms Amendment was incorporated into the $129 billion Labor, Health and Human Resources and Education appropriations bill for fiscal 1988, and contained $310 million for AIDS education efforts overseen by the Centers for Disease Control.

Sen. Jesse Helms (R-North Carolina) initially proposed that none of the money allocated to the CDC could be used for material or activities that promote, encourage or condone homosexuality, illegal drug use or any sexual activity outside marriage.  During floor debate, Sen. Helms displayed sex-positive comic books created by the Gay Men’s Health Crisis in New York and announced that federal money helped to pay for GMHC’s education program.

″If the American people saw these books, they would be on the verge of revolt,″ claimed Helms.

The senator said he showed the comic books to President Reagan and complained that the GMHC had received $674,679 in federal funding to produce the pamphlets. According to Helms, President Reagan looked at a couple of pages, ″shook his head, and hit the desk with his fist.″

Helms then admitted that the comic books were not paid for with federal funds, but said taxpayer dollars did pay for a series of educational sessions he contended were equally offensive.  He said the sessions included assignments to write a personal ad for publication in a gay newspaper and list alternatives to high-risk sex, as well as instruction in the use of safe sex photos.

″I may throw up,″ Helms announced in the Senate chambers.

Sen. Lowell Weicker (R-Connecticut) and Sen. Daniel Patrick Moynihan (D-New York) are the only two Senators to vote against the legislation.  Weicker lectured Helms for moralizing and said his amendment ″means unnecessary lives lost.″

″We don’t have time to get into philosophical or academic or moralistic debates. We’d better do what the experts have told us to do — put our money into research and put our money into education.″

The response from Lori Behrman, spokeswoman for the Gay Men’s Health Crisis, is: ″Jesse Helms, first of all, is playing with the lives of thousands of Americans. It sends a message that the gay community is expendable in this epidemic.″

The Helms Amendment will have a chilling effect on CDC’s ability to stop the spread of AIDS among drug addicts, homosexuals and sexually active heterosexuals, particularly young people.

This is the latest in a long conflict among lawmakers about what federal AIDS education materials should say and how graphic they should be.

October 22, 1987
Worldwide Impact of AIDS Tops Concerns at United Nations

At the 42nd convening of the United Nations, AIDS becomes the first disease ever debated on the floor of the General Assembly.  The UN resolves to mobilize in the worldwide struggle against AIDS.

Learn More.

“AIDS is one of those critical issues, like nuclear weapons, global development, and environmental pollution, which affects the future of all peoples in all countries,” says UN Secretary General Javier Pérez de Cuéllar in his address.

“It is, in many senses, a global combat, and it threatens us with all the consequences of war – not only of massive death tolls and even greater an numbers of disabled,” he said, “but of orphans, of mass displacements, of loss of productivity, of overwhelming and bankrupting demands on financial, administrative and human resources, of fear, anger and panic, and of social instability.”

In closing, Pérez de Cuéllar says:  “We must combat fear with knowledge, panic with reason and isolation with compassion. We must affirm through solidarity that we are but one human family.”

After the World Health Organization gives a presentation on the global status of AIDS, the UN General Assembly designates WHO to lead the worldwide effort to end HIV/AIDS.

February 20, 1988
20,000 March in Manchester Against U.K.’s Section 28

As the conservative government prepares to enact Section 28 to disenfranchise members of the LGBTQ+ community, 20,000 activists take to the streets of Manchester to protest the law.

Learn More.

Section 28 targets the teaching of school children, with the bill prohibiting the promotion or “acceptability of homosexuality as a pretended family relationship.”  It also banned government funding that supported LGBT events, services and programs.

Paul Fairweather, who worked for Manchester’s city council, recalls how he helped organize for what would become one of the largest LGBTQ+ demonstrations in the country’s history.

“There was a sense that the whole community was under threat,” Fairweather told The Guardian.  “There were also lots of questions about Section 28’s possible impact on gay bars and clubs, as well as concerns about the attitude of the police force.”

Concerns about police hostility deter people from joining the demonstration.  About 20,000 people marched, and the event revitalized Manchester’s LGBTQ+ movement.

March 3, 1988
Teen Ryan White Testifies before President’s Commission on AIDS

Ryan White, the Indiana teenager who has become a national spokesperson for AIDS education, testifies before the President’s Commission on AIDS about the stigma he has endured.

May 24, 1988
U.K. Adopts Section 28, Prohibiting Promotion of Homosexuality

United Kingdom authorities enact Local Government Act of 1988, which became notorious for its inclusion of Section 28.  The vaguely worded law prohibited local authorities and schools from “promoting” homosexuality and funding lesbian and gay initiatives.

Learn More.

The clause in question prohibited “the teaching in any maintained school of the acceptability of homosexuality as a pretended family relationship.”

Margaret Thatcher, Britain’s Prime Minister, said at the time: “Children who need to be taught to respect traditional moral values are being taught that they have an inalienable right to be gay. All of those children are being cheated of a sound start in life.”

Section 28 arose within a wider social and political landscape that sought to disenfranchise members of the LGBTQ community.  In 1983, 50% of those surveyed agreed that “sexual relations between two adults of the same sex” were “always wrong.”  By 1987, the figure had risen to 64%, perhaps fuelled by fears associated with the spread of HIV — which was often characterized as “the gay disease.”

One of the original sources of complaint was from someone who objected to Jenny Lives with Eric and Martin, a children’s storybook by the Danish author Susanne Bösche and published in England by Gay Men’s Press. The author’s intention was to give children knowledge about different types of family relationships and she seemed stunned by the subsequent uproar in the U.K.

In 1986, the book was discovered in a library of the Labour-controlled Inner London Education Authority. A National Council for Civil Liberties pamphlet revealed there was only one copy, located in a teachers’ resource centre where access was controlled. Yet an atmosphere of media-stoked paranoia soon arose.

Many LGBT+ people who came of age during the era of Section 28 felt vulnerable to physical and verbal abuse and, because of Section 28, teachers would not step in to protect them.

“School was hard,” said Divina De Campo, a contestant on RuPaul’s Drag Race UK in the 2019 season.  “I got a lot of flak from pretty much everybody in the school. Growing up for everybody was hard, but then you add on being gay and it was just a whole other level.”

Understanding AIDS
May 26, 1988
Surgeon General Launches Nationwide Education Campaign

C. Everett Koop, the U.S. Surgeon General, launches the nation’s first coordinated HIV/AIDS education campaign.  It is the largest public health mailing in history.

Learn More.

Between May 26 and June 30, 1988, the Centers for Disease Control mail the pamphlet Understanding AIDS to every U.S. household.  Approximately 126 million copies were distributed, reaching at least 60% of the population.

The brochure was produced in Spanish as well as English, and its purpose was 3-fold: to clarify how AIDS is transmitted; to emphasize that behavior, not identification with risk groups, put people at risk; and to stimulate informed discussions about AIDS at all levels of society.

In conjunction with the mailing, the CDC initiated contacts with state health departments and manufacturers of AIDS testing kits.  In anticipation of increased requests for information that the brochure would generate, the CDC added up to 1,000 operators to the National AIDS Information Line.

The impact of the campaign on AIDS-related behavior was not fully assessed.  Extensive message pretesting and other marketing techniques designed to improve the effectiveness of the brochure, however, helped Understanding AIDS achieve an increase in awareness and concern about AIDS nationwide.

During the process of the campaign, the CDC learned a number of lessons, including the importance of setting a deadline, doing formative research, and achieving a consensus on scientific knowledge.

July 23, 1988
FDA Approves Importation of Experimental Drugs

The U.S. Food and Drug Administration announces it will allow the importation of small quantities of unapproved drugs for people with life-threatening illnesses, including HIV/AIDS.

August 1, 1988
U.S. Announces Pediatric AIDS Service Grants

The U.S. Health Resources and Services Administration awards $4.4 million in grants to 11 states and Puerto Rico for the first pediatric AIDS service demonstration projects.

Learn More.

The HRSA-funded projects are expected to demonstrate effective ways to:

  • reduce mother-to-child transmission of HIV;
  • develop coordinated, community-based, and family-centered services for infants and children living with HIV; and
  • develop programs to reduce the spread of HIV to vulnerable populations of young people.
October 18, 1988
U.S. Passes Abandoned Infants Assistance Act

The Abandoned Infants Assistance Act becomes law, addressing the issue of so-called “boarder babies.”  These infants, many of whom have been perinatally exposed to drugs or HIV, have been either been orphaned or left at hospitals indefinitely by their parents.

Learn More.

The AIA funds projects to support moving the children into foster care or other more traditional living arrangements.

November 4, 1988
President Reagan Signs Comprehensive HOPE Act

President Ronald Reagan signs the Health Omnibus Programs Extension (HOPE) Act into law, authorizing the use of federal funds for AIDS prevention, education, and testing.

Learn More.

As the first comprehensive federal AIDS bill, it establishes the Office of AIDS Research at the National Institutes of Health (NIH) and the AIDS Clinical Trials Group.

November 7, 1988
NYC Pilots Controversial Needle-Exchange Program

The New York City Health Department begins a pilot needle-exchange program to address the growing number of HIV infections among people who inject drugs

Learn More.

The program is opposed by many of the city’s black and latinx leaders, who see it as an abandonment of IV-drug-using people of color.

The leaders demand a more comprehensive approach to the issue, proposing more resources for drug-prevention education, addiction treatment, and law enforcement.

Intron A and Roferon A
November 22, 1988
FDA Approves Intron A and Roferon A for Treatment of KS

The Food and Drug Administration approves the first drug specifically developed for treating Kaposi’s sarcoma (KS), a leading complication of AIDS.

Learn More.

With the approved FDA licensing, Intron A and Roferon A (human alpha interferon injection) can now be medically administered to patients for the treatment of KS.

The FDA reported that up to 45% of KS patients receiving large doses of alpha interferon ”responded with a significant reduction in the size of their tumors.”  Dr. Kathryn C. Zoon, an F.D.A. official, said that alpha interferon works best in people in the early stages of the disease.

The FDA based its approval on studies involving about 500 patients with KS.  Alpha interferon joined AZT and pentamidine as the only drugs approved in the U.S. for the treatment of AIDS or its related conditions.  Previous treatments for KS were radiation and other cancer drugs.

Alpha interferon was manufactured as Intron-A by the Schering Corporation of Kenilworth, New Jersey, and as Roferon by Hoffmann-La Roche Inc. of Nutley, New Jersey.

November 28, 1988
FDA Approves Ganciclovir for Treatment of Cytomegalovirus Retinitis

The Food and Drug Administration approves ganciclovir, a still-experimental medication for the treatment of cytomegalovirus retinitis in AIDS patients.

Learn More.

Issued under the FDA’s treatment investigational drug protocol, the approval allowed for ganciclovir (GCV) to be issued in a clinical setting, with precautions similar to chemotherapy treatment. Manufactured by Roche Laboratories under the brand name Cytovene, the drug was administered to a patient by intravenous infusion over one hour, a time designed to reduce its toxicity.

Some patients taking GCV experienced a range of serious adverse effects, including granulocytopenianeutropeniaanemiathrombocytopenia, fever, nausea, vomiting, indigestion, diarrhea, abdominal pain, flatulence, anorexia, raised liver enzymes, headache, confusion, hallucination, seizures, pain and phlebitis at injection site, sweating, rash, itch, and increased serum creatinine.  It also could cause bone marrow suppression.

But at the time, GCV was the only FDA-approved treatment for cytomegalovirus retinitis, a condition that in its worst phase caused blindness.

In the years to come, ganciclovir would be followed by other treatments, including foscarnet, cidofovir, and valganciclovir.  While these medications were successful in reducing eye infections, their overall effectiveness was often complicated by toxicities and the development of resistance.

November 29, 1988
U.S. Announces Plan to Expand AIDS Research

The U.S. announces a new program which would engage city doctors, group practices and private clinics in federal AIDS research.

Learn More.

Under the coordination of National Institute of Allergy and Infectious Diseases, the program would issue contracts to doctors for the treatment and data collection regarding thousands of AIDS patients, health officials said.  The program has received a $6 million budget for its first year.

Dr. Anthony S. Fauci, director of NIAID, told the New York Times that the program’s aim was to expand federal research opportunities to doctors and patients who were not affiliated with existing clinical trials.  Dr. Fauci said the program was seeking to involve more Black and Hispanic people, as well as intravenous drug users and sex workers.

In the program, patients using potentially effective but unapproved therapies would be monitored.  The opportunity for patients to receive access to experimental drugs in community settings would be another component of the program, according to health officials.

World AIDS Day 3 (2)
December 1, 1988
Initial World AIDS Day is Observed

December 1st is designated by the World Health Organization as “World AIDS Day.”

Learn More.

Supported by the United Nations, World AIDS Day is observed for the first time with the theme “Join the Worldwide Effort.”  Today, World AIDS Day continues to be observed.

In 2020, there was a reported 37.6 million people across the globe with HIV.  Of these, 35.9 million were adults and 1.7 million were children.

An estimated 1.5 million individuals worldwide would acquire HIV in 2020.  This marks a significant decline (30%) in new HIV infections since 2010, but there is still much work to do.

January 2, 1989
California Legislature Enacts Laws to Criminalize HIV

Eight AIDS bills signed into law by Gov. George Deukmejian during 1988 take effect in California, including three that criminalize HIV and one that weakens rules around doctor-patient confidentiality.

Learn More.

The legislation, proposed by anti-gay Republican Sen. John Doolittle, include:

  • Penalties — SB 1007, which adds three years to prison sentences of those convicted of some sex crimes if they know they are HIV-positive when they commit the crime;
  • Prostitutes—SB 1007, which makes it a felony for a prostitute to continue working after knowing he or she has been exposed to the AIDS virus; and
  • Donors—SB 1002, which makes it a felony to donate blood, semen, breast milk or body organs to another person if the donor knows that he or she is infected with the AIDS virus.

Also going into effect is Democratic Sen. Gary K. Hart’s bill, SB 2847, which allows physicians to tell other medical personnel if a patient has AIDS so they can protect themselves.

January 10, 1989
LA County Prohibits Discrimination against People with HIV/AIDS

On a 3-2 vote, the LA County Board of Supervisors tentatively approves an ordinance prohibiting employers, landlords, schools and businesses in the county’s unincorporated areas from discrimination based on AIDS.

February 7, 1989
Senate Hearings Examine Governmental Response to HIV/AIDS

Sen. Ted Kennedy, chair of the Senate Committee on Labor and Human Resources, holds a series of five oversight hearings to examine how the federal government is combating AIDS.

Learn More.

Education, care, and drug development for HIV/AIDS are key areas of focus of the hearings.

The FDA, CDC, HERSA and Samuel Thier, president of the Institute of Medicine of the National Academy of Sciences, all testify.

West Hollywood Settles HIV Discrimination Lawsuit

The City of West Hollywood settles an HIV/AIDS discrimination case brought by Paul Jasperson, who filed suit against the city and Jessica’s Nail Salon two months earlier, alleging HIV discrimination.

Learn More.

Jaserson’s civil action against the salon, a test case for the West Hollywood’s new HIV discrimination ordinance, is on appeal, with support from Los Angeles, Santa Monica and the American Civil Liberties Union.

June 28, 1989
Rep. Dannemeyer Reads ‘What Homosexuals Do’ into Congressional Record

Given permission to address the U.S. House of Representatives for one minute on the subject of “Homosexuality,” Rep. William E. Dannmeyer commences on an hours-long diatribe about “the gay agenda.”

Learn More.

Apparently upset that gay men are attempting to “delude the public into viewing homosexuality as an innocuous alternative lifestyle,” the six-term Republican Congressman from Orange County, California insisted on reading into the Congressional Record his statement titled “What Homosexuals Do.”

In his statement, Rep. Dannemeyer dove into graphic descriptions of the sex acts he believes all gay men engage in “two or three times a week.”  He contrasted these sex acts with the traditional family values he equated to “the heterosexual ethic” evoked in biblical scripture.

He also denied scientific research that indicated that homosexuality is inherent in individuals from birth and advocated for laws that prohibit homosexual sex acts.  In Dannemeyer’s view, homosexuality is, psychologically, a “deep pathology,” but one that can in effect be cured because “counseling can steer people away from that lifestyle.”

He closed his very long statement with the following:

“As long as I have the pleasure to serve in the U.S. Congress, I will con- tinue to affirm the heterosexual ethic at every turn, with every subtly, with every bit of imagery I can conjure, with the help of good people across this Nation, as well as with the help of a majority of my colleagues in Congress, and also by the grace of God.”

Dannemeyer’s speech drew fire from several of his colleagues, including Rep. Andrew Jacobs Jr. (D-Ind.), who found it “unspeakable.”

Eric Rosenthal, political director of the Human Rights Campaign Fund, told the Washington Post, “Dannemeyer has opposed every single public health consensus about fighting AIDS from every responsible public health official, from (former surgeon general C. Everett) Koop to the AIDS commission to the National Academy of Sciences.  Dannemeyer has been on the other side from day one.”

Rosenthal expressed hopefulness that the majority federal legislators were not like Dannemeyer and would support legislation that funds AIDS research and services.

“People like Dannemeyer and (Senator Jesse) Helms intimidate their colleagues into voting against us, but most members know that’s not what they ought to do, and they really go out of their way to avoid being homophobic,” Rosenthal said.  “I think there’s an underlying sense of fairness in the American people. They don’t necessarily understand lesbians and gays very well, but deep down is a strong opposition to discrimination.”

* * * * *

Congressional Record for the U.S. House of Representatives, Thursday, June 29, 1989

Washington Post, “Out of the Cloakroom: The Anti-Gay Crusade” by Phil McCombs, January 25, 1990

September 19, 1989
National Commission on AIDS Convenes

The National Commission on AIDS meets for the first time at Ford’s Theatre in Washington, D.C.

Learn More.

At the meeting, witnesses testify on the problems facing AIDS patients and what the government is doing in response.

The meeting is facilitated by June Osborn, M.D., who would chair the commission from its inception through 1993.  Dr. Osborn, who serves on WHO’s Global Commission on AIDS, has extensive experience advising the CDC and the FDA on vaccines for diseases such as influenza, hepatitis, and polio.  Osborn would go onto write numerous articles and give many speeches on AIDS and HIV public healthcare policy.

The National Commission on AIDS consists of 15 members: five appointed by the Senate, five by the House, two by President George W. Bush, and the secretaries of Health and Human Services, Defense, and the Veterans Administration.

Perhaps the most recognizable member of the National Commission on AIDS, is former NBA star Earvin ‘Magic’ Johnson.  However, Johnson would resign from the commission in September 1992, writing to President Bush:  “I cannot in good conscience continue to serve on a commission whose important work is so utterly ignored by your administration.”

Johnson’s resignation is preceded by another six months earlier of Harlon D. Dalton, a Yale Law School professor who is the only other African American appointed to the commission.  In March 1992, Dalton would complain about the lack of action from black politicians, saying, “Any high-visibility politician can point to the one time a year where [AIDS] is mentioned. But there haven’t been any votes there. Gay black men don’t exist, black men don’t vote and babies don’t vote.”

At its first meeting, Chair Osborn gives recognition to Rep. J. Roy Rowland, who she refers to as “the Father of the Commission.”  Rep. Rowland is the principal sponsor of the legislation that created the commission on Nov. 4, 1988.

Other members include:
  • Dr. David E. Rogers, head of the New York City Mayor’s Task Force on AIDS and New York State’s AIDS Advisory Council
  • Diane Ahrens, Minnesota local government official
  • Rev. K. Scott Allen, a Baptist minister, coordinator of the AIDS Interfaith Network in Dallas
  • Don C. Des Jarlais, a NY physician who advocates for needle-exchange programs
  • Eunice Diaz, community affairs director of White Memorial Medical Center in Los Angeles
  • Mary D. Fisher, appointed by Bush to replace Magic Johnson in October 1992
  • Donald S. Goldman, New Jersey attorney, author on ethical issues involved in AIDS treatment
  • Larry Kessler, executive director of AIDS Action Committee of Massachusetts
  • Charles Konigsberg, Jr., director at the Kansas Department of Health and Environment
  • Belinda Mason, journalist who dies of AIDS-related illnesses in September 1991

The commission was established by a statute enacted November 4, 1988, with the aim of “promoting the development of a national consensus on policy concerning AIDS.”. It produced several reports over the next 4 years.

The commission approaches its work through numerous hearings, covering the following topics:

  • healthcare, treatment, and international aspects of the HIV epidemic;
  • Federal, State, and Local responsibilities;
  • the Southern California epidemic;
  • social and human issues;
  • Executive and Legislative branch issues;
  • current research and clinical trials;
  • HIV epidemic in the Commonwealth of Puerto Rico;
  • African American communities;
  • Pediatric and Adolescent HIV;
  • Lesbian, Gay, and Bisexual communities among Asians, Asian Americans, and Pacific Islanders;
  • Women and HIV disease and civil rights;
  • religious communities response; and
  • risks of transmission in healthcare settings.
November 26, 1989
AIDS-Care Activist Chris Brownlie Dies

AIDS-care activist Chris Brownlie, for whom the first Los Angeles County-supported AIDS hospice was named, dies of AIDS-related illness at his Silver Lake home at the age of 39.

Learn More.

Born in Farmington, NY, Brownlie had been active in LGBTQ politics since the early 1970s, when he helped found the Los Angeles Gay Community Services Center.

Since the mid-1980s, the one-time greeting card company owner also worked for a variety of AIDS-care projects, including service as a volunteer for AIDS Project Los Angeles (APLA) and the Minority AIDS Project.  He also helped found the nonprofit AIDS Hospice Foundation, an outgrowth of the 1986 Stop AIDS Quarantine Committee, which defeated a state ballot initiative that would have required detention of those testing positive for the human immunodeficiency virus.

Faced with inaction by the then-conservative Los Angeles County Board of Supervisors, Hospice Foundation members picketed in front of Supervisor Mike Antonovich’s home.  Brownlie, meanwhile, appeared before the LA County Commission on AIDS, emotionally demanding: “You find a way for me to die at home in the arms of my loved ones, or a facility in which my loved ones can care for me in dignity.”

When supervisors eventually voted $2 million for AIDS health care, the Hospice Foundation agreed to operate a facility in Elysian Park at the site of Barlow Hospital’s old nursing quarters.

The 25-bed facility was named the Chris Brownlie Hospice, according to foundation President Michael Weinstein, “because he is a representative of those in the community who have the spirit, courage and grace to fight for those with AIDS.”

The Chris Brownlie Hospice, which had a waiting list in late 1989, was the largest of its kind in the county and offered 24-hour medical service.  At that time, construction was under way on another 25-bed hospice to be operated by the foundation on the grounds of Metropolitan State Hospital in Norwalk.

“If you want a miracle that is better than any drug, work to make life better,” Brownlie said at the start of construction of the Chris Brownlie Hospice.

“Of course, I’ve always hoped that I would not die, that I would live forever,” Brownlie told The LA Times when the facility opened.  “But on another level, I actually get a sense of well-being about this experience.  Sometimes it becomes very profound in a religious sense at the edges of my consciousness.  And this is what the hospice program is about.  It will help others accept the fact that death, too, is part of the life experience.”

Shortly after traveling to Sonoma, Arizona for a vacation with his longtime partner, Phill Wilson, Brownlie became very ill and eventually slipped into a coma.

He was cared for at his namesake hospice, where he would occasionally wake up from the coma and talk with Wilson.

“Finally, after about eight or nine days of that, he woke up and he said, ‘Take me home.’  I knew what he meant, and so I said, ‘We’re going home,’ and nobody agreed,” Wilson told PBS’s Frontline in a 2004 interview.  “The doctor said no; the nurses said no; all of our friends said no.  They didn’t think that I could take care of him.

“I brought him home, and we [got] a little hospital bed and all the supplies, and I kept saying, ‘We won’t need all of that; we won’t need all of that,’ because I knew that he wanted to come home to die.  He wanted to come home so that the last minutes would be in our space, and so we brought him home.”

Wilson said he carried Brownlie into the house, put him into bed and sat with him.  After taking a short nap at the suggestion of the home nurse, Wilson returned to Brownlie’s room and found him “breathing the kind of labored breathing [where] you can kind of hear death happening.”

Wilson said he climbed into bed with Brownlie and whispered that it was okay now, it was going to be OK, and that he was going to be OK.

He sang to Brownlie a favorite song, “Let Me Call You Sweetheart.”

“The words are ‘Let me call you sweetheart/ I’m in love with you/ Let me hear you whisper/ That you love me, too,'” Wilson recalled.  “And he took a breath, and then he didn’t take another breath.”

HRSA Funds States with $20M for HIV Care & Treatment

The U.S. grants $20 million for HIV care and treatment through the Home-Based and Community-Based Care State grant program, introducing HIV care and treatment to many states that have no programs.

Learn More.

In its supporting report, the Health Resources and Services Administration notes that only six states have Medicaid program waivers for the treatment and care of people with HIV/AIDS: California, Hawaii, New Mexico, New Jersey, Ohio and South Carolina.  The waiver services cover case management, personal care and adult day care in five of the six states.

States with these programs report that the AIDS-specific waiver enables them to establish a uniform system of services, a network of treatment options, and greater access to home and community-based care for people with AIDS, the report states.

Perhaps most importantly, the programs expand financial eligibility for those needing care and treatent.

The newly announced HRSA grant program provides funding so that all states can adopt and strengthen programs that target AIDS-specific services to those who need them.

U.S. Launches Precursor to Ryan White CARE Act

A CDC/HRSA initiative provides $11 million to fund seven community health centers to provide HIV counseling and testing services. This is a precursor to what will be part of the Ryan White CARE Act.

July 26, 1990
Congress Passes Americans with Disabilities Act

The U.S. Congress enacts the Americans with Disabilities Act. The Act prohibits discrimination against individuals with disabilities, including people living with HIV/AIDS.

August 18, 1990
U.S. Enacts Ryan White CARE Act with $220M in Funding

The U.S. Congress passes legislation providing $220.5 million in federal funds for HIV community-based care and treatment services.

Learn More.

Titled the Ryan White Comprehensive AIDS Resources Emergency (CARE) Act, the legislation is named for the Indiana teen who became infected through treatment for his hemophilia and died in April 1990.

This creates the nation’s largest HIV-specific federal grant program, and the U.S. Health Resources and Services Administration is charged with managing the resources,

Blood screening
September 16, 1990
Lawsuits Filed against Blood Agencies over Tainted Transfusions

The blood services industry braces itself against more than 300 lawsuits regarding people infected with the AIDS virus through blood transfusions.

Learn More.

A small number of the medical negligence lawsuits have been settled for large amounts of money, and another 300 lawsuits are headed to trial, mostly in San Francisco, New York and Los Angeles, the Los Angeles Times reported.

While eight years has passed since the first medical reports made connections between transfusions and AIDS, legal cases are only beginning to surface because of the lag time between becoming infected with HIV and onset of physical symptoms.  An estimated 26 million people received transfusions between 1977 and 1985, years when the AIDS epidemic spread largely unchecked.

Legal experts expect thousands more cases to be filed in the courts over the next few years as more people discover that they were given tainted blood during the early years of the AIDS epidemic.

In one case, a 5-year-old Arizona boy was awarded $28.7 million — believed to be the largest such award — and several other jury verdicts have been in the range of $12 million.

“These awards are far higher than in other types of cases, because the jury tries harder because of the disease, because they have all personally felt that fear,” attorney Duncan Barr told the LA Times.  Barr had defended San Francisco’s Irwin Memorial Blood Bank in several cases.

Plaintiffs have argued that the blood banks ignored scientific warnings about the threat of HIV-contaminated blood, failed to screen out high-risk donors through questionnaires that identified high-risk behavior, and refused to perform tests for other diseases that were often present in HIV-infected donors.

In Los Angeles County, health officials said 194 adults and 36 children have contracted AIDS through transfusions.

The American Red Cross, which collects half the nation’s blood supply, would not comment to the LA Times on how many lawsuits have been filed against it over allegedly tainted blood transfusions.

The Blood Council of Community Blood Centers released a statement saying that most centers were insured only for $2 million to $5 million a year for the years in question, and if the centers run out of insurance funds, they may be forced to increase the cost of blood sales to hospitals or go bankrupt.

January 1, 1991
HOPWA: Federal Housing Assistance Program Launched

Congress enacts the Housing Opportunities for People with AIDS Act of 1991, the first and only federal housing program solely dedicated to providing rental housing assistance for persons and their families living with HIV/AIDS.

Learn More.

Approved as part of the Cranston-Gonzalez National Affordable Housing Act of 1990, HOPWA funds short-term and permanent housing, together with supportive services, for individuals living with HIV/AIDS and their families.

A report by the Congressional Research Service titled “Housing for Persons Living with HIV/AIDS,” describes HOPWA as a way to address the financial vulnerability and likelihood of homelessness associated with AIDS.

“Research has indicated that individuals living with HIV who live in stable housing have better health outcomes than those who are homeless or unstably housed, and that they spend fewer days in hospitals and emergency rooms,” the report states.

The U.S. Department of Housing and Urban Development (HUD) is charged with the administration of the funding, working with state and local community housing programs.

July 21, 1991
U.S. Pushes States to Restrict HIV+ Workers

The U.S. Centers for Disease Control and Prevention recommends restrictions on the practice of HIV-positive healthcare workers, prompting Congress to enact a law requiring states to adopt the CDC restrictions.

Learn More.

The CDC’s report ecommends that healthcare workers who are HIV-positive “should not perform exposure-prone procedures unless they have sought counsel from an expert review panel and been advised under what circumstances, if any, they may continue to perform these procedures.”

The CDC goes on to say that HIV-positive healthcare workers should notify prospective patients of the worker’s HIV status before they undertaking exposure-prone invasive procedures.

The report cites the case of Dr. David Acer, a dentist with AIDS who likely transmitted HIV to five of his 850 patients.

Although this was the only cluster of health care worker-to-patient transmissions of HIV in the U.S., the report concerning Dr. Acer immediately set off public debate on the effectiveness of existing safeguards of the public’s health, whether it was appropriate for HIV-positive health care workers to practice, and the public’s right to know the HIV status of their physicians.

August 14, 1991
U.S. Creates Network of Clinical Trials, Expanding Treatment Options

Congress passes legislation to create a network of community-based clinical trials for HIV treatment.

Learn More.

The Terry Beirn Community-Based Clinical Trials Program Act establishes a network of community clinical trials to complement the National Institute of Allergy and Infectious Diseases’ university-based research in order to provide increased access to experimental therapies.

The legislation is named for Terry Beirn, a program officer for amfAR who worked on the Senate Committee on Labor and Human Resources on AIDS legislation.

Known as a fierce AIDS activist, Beirn com­pil­ed quar­terly direc­to­ries of AIDS treat­ment for doc­tors and patients, fundraised for AmFAR and other research orga­ni­za­tions, and pushed leg­is­la­tion to fund clin­i­cal tri­als of exper­i­men­tal treat­ments and drugs.

Following his diag­nosis with AIDS in 1984, Beirn began his advocacy work on AIDS policy with Sen­. Ted Kennedy, and in 1986, Beirn joined the staff of the U.S. Sen­ate Com­mit­tee on Labor and Human Resources. Dur­ing his time there, Beirn gar­nered sup­port for the first com­pre­hen­sive piece of AIDS leg­is­la­tion, the HIV Organ Pol­icy Equity Act of 1988, which mod­i­fied rules regard­ing organ dona­tion between HIV-pos­i­tive indi­vid­u­als.  In 1990, Beirn would be instru­men­tal in the pas­sage of the Ryan White Care Act, for which he advo­cates directly with Pres­i­dent George H.W. Bush.

Beirn dies of AIDS-related illness in 1991 at the age of 39.

August 16, 1991
U.S. Travel Ban Causes Int’l AIDS Conference to Move to Amsterdam

The 8th International AIDS Conference is originally scheduled to be held in Boston in 1992, but conference planners decide to move it to Amsterdam due to U.S. immigration restrictions on people living with HIV/AIDS.

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Harvard University, which is co-sponsoring the conference with the World Health Organization, announces that because of “continuing uncertainty” of the country’s policy toward HIV-positive individuals, it will not hold the 1992 conference in Boston.  Weeks later, Harvard would announce that the next conference would be held in Amsterdam.

The Boston site of the meeting is canceled, because of Bush Administration requirements that short-term visitors to the U.S. declare whether they are infected with the AIDS virus.  The policy bans travel to the U.S. by foreigners infected with the virus, unless they get a waiver.

Two months earlier, the 1991 International AIDS Conference in Florence closes with officials and participants marching to the U.S. Consultate to protest the American travel ban.

Almost 20 years later, the ban on HIV-positive immigrants and travelers to the U.S. would be lifted by an executive order by President Barack Obama.

AIDS Quilt - Stan Hadden
December 2, 1991
Sacramento Activist Stan Hadden Dies

Stan Hadden, a senior administrative aide to California Senate President Pro Tempore David A. Roberti and one of the most influential voices on AIDS policy in Sacramento, dies of AIDS-related illness at the age of 35.

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As fierce fighter for HIV/AIDS policy for 10 years, Haddon is credited with shepharding the creation of the California AIDS Advisory Committee in 1983 and writing legislation supporting a coordinated approach to local HIV/AIDS programs and services in 1985.

According to Stephen Colbrook’s paper “Clandestine Networks and Closeted Bureaucrats: AIDS and the Forming of a Gay Policy Network in California,” Haddon was a key player among policymakers who jumped into action when the AIDS crisis unfolded.  When Hadden learned that a new deadly disease was spreading through San Francisco’s gay community, he brought the epidemic to the attention of his boss, David Roberti, who was the president of the California senate.

Colbrook wrote:

“Hadden quickly emerged as a pivotal figure in California’s response to the AIDS crisis. He was affable, forthright, and pragmatic, burnishing a well-deserved reputation as the AIDS Tsar of California.  By 1987, his monthly AIDS newsletter had 25,000 subscribers, and his correspondence reached beyond California to activists in Texas, Illinois, and New York.”

Sen. Roberti provided Hadden with a significant degree of autonomy, with which Hadden used to craft a large portion of California’s early AIDS legislation, including Senate Bill 1215, which expanded the state budget for prevention education by $11 million.  Passed in 1985 by an overwhelming bipartisan majority in both the Assembly and Senate at a time when budget funds were thin, SB 1215 cemented California’s leading role in addressing the HIV/AIDS crisis.  In 1985, nearly half of the total state spending on the AIDS epidemic was attributed to California, according to Colbrook.

Hadden’s leadership also throughout the 1980s also helped steer California’s action on the epidemic toward a focus on patient confidentiality and individual rights.  This focus was not always adopted by other states in their approach to the AIDS crisis.  On the other end of the spectrum was Texas, whose political leaders created policy centered on the disease’s perceived threat to the heterosexual population.

Hadden was one of only a few in the 1980s Sacramento political scene who were open about their LGBT identity, journalist Karen Ocamb would later write in The Pride.  Scores of administrative and political aides to California legislators remained in the closet, fearful that open knowledge of their sexual identity would end their professional careers.  Elected officials and potential candidates who identified as LGBT also remained silenced by the very real fear of ruination.

In the final two weeks of his life, Hadden received round-the-clock nursing care as part of a hospice program.  Sacramento AIDS Foundation spokeswoman Patty Blomberg noted that the AIDS care Hadden received might not have existed if it were not for his influence and persistence.

Blomberg told the Sacramento Bee that Hadden had slipped into a coma early that morning and then died at about noon at his farmhouse along the Sacramento River, surrounded by friends and family who had flown in from as far away as Michigan.

Hadden’s funeral would bring in friends and colleagues from around the state, including Ocamb and John Duran, then President of the Board of LIFE AIDS Lobby who would become Mayor of the City of West Hollywood.

“In a gesture unheard of for the suits of Sacramento, a huge rainbow flag was unfurled and solemnly marched down the street to the Capitol,” Ocamb recalled.

“Stan’s memory will go on, because he made a contribution to this state that many of us can only dream of making,” Senate President Pro Tem Roberti said during Hadden’s memorial service at St. Francis Church in midtown Sacramento.

December 1, 1992
CDC Extends HIV Education Programming to Business Community

The U.S. Centers for Disease Control and Prevention initiates a long-term, primary prevention program for HIV education directed at business owners and the labor community.

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The Business Responds to AIDS program is designed to help large and small businesses meet the challenges of HIV/AIDS in the workplace and the community.

In an interactive teleconference originating at its Atlanta headquarters, the CDC introduces business leaders to the BRTA program and releases resources to assist them with initiating their own HIV-education programs in the workplace.

Participants in the teleconference include the American Red Cross, the U.S. Department of Health and Human Services, the New England Corporate Consortium on AIDS, and the business and labor communities from several sites throughout the U.S.

The CDC encourages businesses to develop written HIV policies and provide employee education about preventing HIV transmission.

In three years, the CDC would follow up BRTA with the Labor Responds to AIDS program in 1995.

January 23, 1993
President Clinton Establishes Office of National AIDS Policy

As one of his first acts in the White House,  President Bill Clinton establishes the White House Office of National AIDS Policy.

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The Office of National AIDS Policy (ONAP) is designed to oversee U.S. efforts to implement the President’s National HIV/AIDS Strategy.

ONAP’s scope would grow over the next twenty years to include coordinating national and global efforts with the National Security Council and the Office of the Global AIDS Coordinator.  The group would work closely with international bodies to ensure that the U.S. response to the global pandemic is fully integrated with other prevention, care, and treatment efforts around the world.

ONAP would be featured in the press again in January 2017, when under the new Trump administration, the office’s website would become inaccessible.  It is then reported that the office closed with the departure of the previous director, Obama-appointee Amy Lansky, with no clear plans if or when President Trump would reopen it.

When President Trump fails to appoint a new ONAP director by June 2017, six members of the Presidential Advisory Council on HIV/AIDS file letters of resignation, citing that above all things the Trump administration “simply does not care” about the HIV/AIDS situation in the U.S.

Then in late December 2017, Trump would fire the remaining members of the council with a form letter sent via FedEx.

In June 2021, President Joe Biden would restore ONAP with the appointment of Harold Phillips, a Black man living with HIV, as Director.  News of Phillips’s appointment would arrive June 5, the 40th anniversary of the first reports of AIDS.

June 10, 1993
U.S. Expands Scope for Women/Minorities as Research Subjects

Congress enacts the NIH Revitalization Act and directs the National Institutes of Health to expand involvement of women and minorities in all research.

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The Act gives the Office of AIDS Research primary oversight of all NIH AIDS research and requires the NIH and other research agencies to increase the role of women and minorities as research subjects.

The statute calls for outreach to women and members of minority groups for recruitment as subjects in clinical research projects.  For clinical trials in which women or members of minority groups are included as subjects, trials must be designed and executed in a manner that allows for researchers to determine whether the variables being studied in the trial affect women or members of minority groups differently than other subjects in the trial.

June 10, 1993
U.S. Immigration Ban Codified into Federal Law

Slipped into the NIH Revitalization Act is an amendment that codifies the U.S. HIV immigration ban into law, which President Bill Clinton signs.

June 13, 1993
LA Activist & Commissioner Rand Schrader Dies

Rand Schrader, a California municipal judge who was a noted gay activist, dies of AIDS-related illness at Century City Hospital. He was 48.

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Judge Schrader helped establish the AIDS clinic at the Los Angeles County Medical Center (which would be renamed in his honor).  He became one of California’s first openly gay judges when he was appointed to the Municipal Court in 1980 by Gov. Ed Brown.  He also served on the Board of Regents for the University of California, and the board of the Municipal Elections Committee of Los Angeles (MECLA), the first LGBT political action committee.

As a gay, liberal student at UCLA School of Law, Schrader volunteered countless hours giving legal guidance to members of the Los Angeles LGBT Center (then called the LA Gay Community Services Center).  Many of his cases involved police discrimination against gay men.

After graduating from UCLA, Schrader began working for the Los Angeles City Attorney’s Office, becoming the first openly gay staffer.

“He was a star performer,” said LA City Attorney Burt Pines.  “In a relatively short period of time, he had the respect of everyone he worked with, including real conservative prosecutors who thought they could never work with a gay [man].”

In 1987, the county established an AIDS commission, and Schrader was among its first body of commissioners.  At the time, LA County had surpassed San Francisco in the number of HIV/AIDS cases, and yet county officials had refused to acquiesce to activist demands of a ward for the exclusively care and treatreatment of AIDS patients.

As a commissioner, Schrader found himself siding with AIDS activists from ACT UP Los Angeles, who routinely staged demonstrations at the LA County Medical Center.  The activists argued that persons living with HIV/AIDS needed their own ward to protect them from discrimination and neglect.

Schrader disagreed with the commission’s current chairman, Rabbi Allen Freehling.  Chair Freehling said he was concerned that patients put in a separate ward would feel “isolated.”  The commission decided to form a task force to determine a course of action, and soon it became apparent to all the commissioners that people living with AIDS would benefit significantly from having access to their own clinic.

In 1988, the County opened a separate ward for AIDS patients at the county hospital.  The next year, Schrader was elected chair of the AIDS Commission.

When Schrader was diagnosed with HIV in 1991, he went public with the news and continued his judicial work.  A month before Schrader’s death, the LA County Board of Supervisors unanimously approved a motion to name the county’s AIDS ward after Schrader in tribute to “his courage, his vision and his tenacity.”

Today, the University of Southern California maintains responsibility for the Rand Schrader HIV Clinic.  Dr. Joseph Cadden, an infectious disease specialist, serves as Medical Director of more than 40 faculty members who provide primary and specialty care to more than 3,000 patients.

AIDS Quilt - Keeston Lowry
August 29, 1993
Portland Legislative Aide Keeston Lowery Dies

Keeston Lowery, an aide to Portland Commissioner Michael Lindberg,  dies of AIDS-related illness at the age of 43.

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Lowery was a tireless and supremely effective advocate for LGBTQIA+ rights from inside the Portland government.  He also worked as a physical therapist for Emanuel Hospital and served on the Board for the Right to Privacy PAC (predecessor to Basic Rights Oregon).

In 1967-68, Lowery worked on Sen. Robert Kennedy’s campaign for President, and shortly afterward, graduated from Mississippi State University’s five-year occupational therapy program. He continued his higher education and earned another degree from the University of Arkansas. He then worked in Pine Bluff and Little Rock, Arkansas, and in the mid-1970s, he took a job with then-Arkansas Attorney General Bill Clinton.

Lowery moved to Portand, Oregon in 1977 to take a job as a physical therapist for Emanuel Hospital, and quickly became a leader in the local queer community.  He became an aide to Portland City Commissioner Mike Lindberg, and immediately used his role in inter-governmental relations and film policy to cultivate advocates for equal rights in all levels of local and state government.

Lowery crafted Portland’s first civil rights ordinance, which banned discrimination based on race, religion, gender, sexual orientation, and several other categories.

“His beaming smile, southern drawl and good will were infectious,” writes the Gay & Lesbian Archives of the Pacific Northwest in its tribute to Lowery.  “He was an astute political observer who could intuitively plot winning strategies.  His manifold contributions continue to this day, not only in the policies he crafted on behalf of marginalized people, but in memories of all the powerful and empowered people whose lives he touched.”

Lowery’s work on the city’s film production policies and the good will he established with film crews led to his receiving a “thank you” credit on the 1991 film My Own Private Idaho, written and directed by Gus Van Sant.

When Lowery in late August of 1993, Oregon Governor Barbara Roberts and Portland Mayor Vera attended his funeral, held on Sept. 2 in the Rose Gardens at Washington Park, along with numerous members and leaders in the LGBTQIA+ community.  Lowery’s ashes were scattered on Mount Hood, a potentially active volcano in the Cascade Volcanic Arc, located about 50 miles east-southeast of Portland.

The City of Portand’s archives store Lowery’s papers and artifacts.

AIDS Quilt - Michael Callen
December 27, 1993
Pioneer of AIDS Activism Michael Callen Dies

AIDS movement pioneer Michael Callen dies of AIDS-related illness at Midway Hospital in Los Angeles at the age of 38.

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Callen was diagnosed early in the epidemic — 1982 — and he responded by becoming involved in every way he could in promoting the self-empowerment of People With AIDS.  In fact, Callen is credited with coining the term “People With AIDS,” and insisted on this term instead of the passive and negative-sounding phrase “AIDS victim” commonly used at the time.

Callen was born in Rising Sun, Indiana and raised in Hamilton, Ohio.  He graduated in 1977 from Boston University, which he attended on a music scholarship, and then moved to New York, where he sang in cabarets and with the New York City Gay Men’s Chorus.

He grew into political advocacy after receiving a diagnosis of AIDS in 1982.  He became an early proponent of safer-sex practices, writing How to Have Sex in an Epidemic: One Approach with Richard Berkowitz, Dr. Joseph A. Sonnabend, and Richard Dworkin in 1983.

Among the very first publications to recommend the use of condoms to prevent the transmission of STDs in men having sex with men, the pamphlet was distributed at gay social establishments throughout New York City — 5,000 copies in its first run.

That same year, Callen was a plaintiff in the nation’s first AIDS discrimination lawsuit, when Dr. Sonnabend, his physician, successfully fought eviction from a Greenwich Village co-op for treating people with AIDS.  Also in 1983, Callen was a founding board member of the Lesbian and Gay Community Services Center in Greenwich Village.

On August 1, 1983, Callen was one of three PWAs who testified before a Congressional subcommittee examining the U.S. government’s response to the AIDS crisis.  In his statement before Congress, Callen described how he began to feel ill in 1981 and then was diagnosed in the summer of 1982 after being hospitalized with cryptospordiosis.

“It is very difficult when you pick up newspapers or turn on the television, and you hear that no one has fully recovered from this syndrome, and that 80% of those diagnosed with the syndrome are dead after two years,” he said.

A talented writer, Callen became the first editor of the PWA Coalition Newsline and edited the two-volume set Surviving and Thriving with AIDS, published by the Persons With AIDS Coalition in 1988.  From 1988-1989, he was editor of AIDS Forum, and his book, Surviving AIDS, published by Harper/Collins in 1990, received honorable mention from the American Medical Writers Association.

Callen wrote extensively on the subject of the politics of sexuality, his essays regularly appearing in magazines, journals, books, and newspapers, including the Village Voice, The New York Native, and Outweek.  He was among the first to give AIDS a human face, by making courageous appearances on TV shows such as Nightline, Good Morning America and 20/20.  He also appeared on the talk shows Phil Donahue and Geraldo.

Callen moved from New York to West Hollywood to keep up with his busy TV and film schedule.  He can be seen in several films and documentaries, including Philadelphia, Zero Patience, and the HBO documentary Why Am I Gay?

Throughout the years of his illness, Callen had a devoted and caring partner in Richard Dworkin, whom he met in June 1982, when Dworkin answered his classified ad seeking gay musicians.

“I called and Michael answered and said, ‘I happen to be getting together with a bass player tonight, do you want to come over?’  So I said OK and went to his house on Jones Street, and there was the bass player, and Michael had made sorbet,” Dworkin told Tim Murphy of The Body.  “And we fell in love that night, and I stayed over.  He had a piano and books, and to me that was a draw.  He moved in with me in the fall of ’82.”

“Michael accomplished so much in the 11 years between his diagnosis and his demise,” Dworkin wrote in his tribute to Callen on Callen-Lorde, the website for the Callen-Lorde Community Health Center in New York City (named for Michael Callen and Audre Lorde).

Dworkin listed Callen’s many achievments, including the founding of the People with AIDS Coalition, the Community Research Initiative, and the People with AIDS Health Group.  He also mentioned that Callen performed with The Flirtations, “the world’s first gay male politically correct a cappella group,” plus Dworkin helped Callen record and release two solo albums.

Callen also wrote, along with Oscar winner Peter Allen and Marsha Malamet, the song “Love Don’t Need a Reason”  Callen would go on to sing this at numerous events, including AIDS walkathons in New York, San Francisco and Los Angeles as well as the 1993 March on Washington for Lesbian, Gay and Bi Equal Rights.

Shortly before his death, Callen completed vocal tracks for 48 new songs, 29 of which were released as a double album, Legacy (winner of four Gay & Lesbian American Music Awards).

July 28, 1995
President Clinton Creates Advisory Council on HIV/AIDS

President Bill Clinton establishes his Presidential Advisory Council on HIV/AIDS to provide advice, information, and recommendations to his administration regarding HIV/AIDS.

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The Council meets for the first time on this day in 1995.

PACHA focuses on programs, policies, and research that address HIV/AIDS, including the consideration of common co-morbidities of those infected with HIV as needed to promote effective HIV prevention and treatment.

The Council continues to exist and provide advice for each successive Presidential Administrations.

December 6, 1995
President Clinton Holds White House Conference on HIV/AIDS

The President and Vice President convene the first White House Conference on HIV/AIDS in the history of the epidemic, bringing together more than 300 experts, activists and citizens from across the country for a discussion of key issues.

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During the conference, President Clinton shows the country the human face of AIDS and the toll the epidemic is taking on parents, families and communities.

The President also introduces steps and goals to accelerate progress toward a vaccine and a cure.  He urges Congress to maintain the Medicaid safety net; Medicaid pays for the care of nearly half of Americans living with AIDS, including more than 90% of children with AIDS.

Some conference attendees were disappointed, however, that the President did not voice support for government-sponsored needle distribution and exchange programs.

More than 250 participants from 37 states and Washington D.C. are invited to attend the White House conference. In the morning, participants assemble into nine working groups for in-depth discussions on research, substance abuse treatment, transmission prevention, international issues, discrimination, housing and services.

Following lunch, participants gather to observe a plenary session in the Cash Room of the Treasury Building, the focus of which is a roundtable discussion with the President.  One representative from each of the morning’s working groups join the President at the roundtable, along with Director of the Office of National AIDS Policy Patsy Fleming, Secretary of Health and Human Services Donna Shalala, and Dr. Scott Hitt, Chairman of the Presidential Advisory Council on HIV/AIDS.

Also joining the roundtable are two Americans personally impacted by the AIDS crisis: Sean Sasser of Atlanta, who tested positive for HIV at age 19 (best known for his relationship with activist and reality TV star Pedro Zamora) and Eileen Mitzman of New York, who lost her 26-year-old daughter Marni to AIDS in 1991.

January 1, 1996
UN Creates Joint Program to Strengthen AIDS Response

The Joint United Nations Programme on HIV/AIDS is launched to strengthen the way in which the UN is responding to AIDS.

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UNAIDS takes an innovative approach, bringing together various UN organizations to coordinate advocacy for global action on the epidemic.

The launch of UNAIDS involved “a long series of meetings, reports, working groups, whispered conversations and angry confrontations in corridors and telephone calls around the world,” according to UNAIDS: The First 10 Years.

With a staff of 91 in the Geneva-based Secretariat and 10 in various regions, the fledgling organization
quickly learns how to act on its ambitious agenda.

Political advocacy was high on UNAIDS’ list of priorities.  By June 1996, UNAIDS staff had met with political, economic and social leaders in more than 50 countries to brief them on UNAIDS’ mandate and work.

Sally Cowal, Director of External Relations at UNAIDS, would be worried about not having a medical background.

“But as I came to understand more about the epidemic,” Cowal says, “it became clear to me that the political motivation around it, the need to overcome denial and complacency, were probably as important as anything we could do.”

FDA Accelerates Approval of HIV Tests & Therapies

The U.S. Food and Drug Administration approves several new tests and HIV treatments in a three-month period.

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Among its fast-track approvals are:

  • the first HIV home testing and collection kit (May 14)
  • a viral load test, which measures the level of HIV in the blood (June 3)
  • the first non-nucleoside reverse transcriptase inhibitor (NNRTI) drug, nevirapine (June 21)
  • the first HIV urine test (August 6)
May 20, 1996
Congress Reauthorizes Ryan White CARE Act

Congress reauthorizes the Ryan White CARE Act, continuing federal funding for primary medical care, essential support services, and medications for low-income people with HIV/AIDS.

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The legislation grants the funding needed for the U.S. Health Resources and Services Administration to continue its public health response to HIV.

May 18, 1997
President Clinton Sets Goal of HIV Vaccine by 2007

President Bill Clinton announces that the goal of finding an effective vaccine for HIV in 10 years will be a top national priority, and calls for the creation of an AIDS vaccine research center at the National Institutes of Health.

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President Clinton would dedicate the new Dale and Betty Bumpers Vaccine Research Center on June 9, 1999.

September 26, 1997
FDA Approves First Antiretroviral Drug Combo

The U.S. Food and Drug Administration approves Combivir, the first one-pill combination of the two most widely used antiretroviral medications for AIDS and HIV infection.

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A combination of Retrovir (zidovudine or AZT) and Epivir (lamivudine or 3TC), Combivir decreases the number of pills people with HIV have to take daily.

As the first combination agent, the medication significantly simplies HIV therapy.  Combivir becomes the gold standard nucleoside “backbone” until the mid-2000s, when the introduction of newer fixed-dose combinations with improved tolerability and toxicity arrive.


November 21, 1997
Congress Pushes FDA to Accelerate Drug Approval Process

Congress enacts the Food and Drug Administration Modernization Act of 1997, codifying an accelerated drug-approval process and allowing dissemination of information about off-label uses of drugs.

April 20, 1998
Federal Funding Continues to be Withheld from Needle-Exchange Programs

Donna Shalala, Secretary of the U.S. Department of Health and Human Services, determines that needle-exchange programs are effective and do not encourage the use of illegal drugs, but the Clinton Administration refuses to lift the ban on use of Federal funds for these programs.

June 25, 1998
SCOTUS Rules ADA Covers People Living with HIV

The U.S. Supreme Court rules that the Americans with Disabilities Act covers those in earlier stages of HIV disease, not just those who have developed AIDS.

October 12, 1998
Congress Approves Funding for Hemophilia Relief

Congress enacts the Ricky Ray Hemophilia Relief Fund Act, honoring the Florida teenager infected with HIV through contaminated blood products.

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The Act authorizes payments of $125,000 to individuals with hemophilia and other blood clotting disorders who were infected with HIV by unscreened blood-clotting agents between 1982 and 1987.  The funding program also includes payments for individuals who were infected with HIV through perinatal transmission from a hemophiliac parent.

President Clinton Declares Crisis in Minority Communities

President Clinton declares AIDS to be a “severe and ongoing health crisis” in black and hispanic communities in the U.S. and announces a special package of initiatives aimed at reducing the impact of HIV/AIDS on racial and ethnic minorities.

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The initiative invests an unprecedented $156 million to improve the nation’s effectiveness in preventing and treating HIV/AIDS in minority communities.

The funding is spread across three broad categories: technical assistance and infrastructure support; increasing access to prevention and care; and building stronger linkages to address the needs of specific populations.

November 12, 1998
Congress Allocates $156 Million for Minority AIDS Initiative

With the leadership of the Congressional Black Caucus, Congress funds the Minority AIDS Initiative.

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An unprecedented $156 million is dedicated to improving the nation’s effectiveness in preventing and treating HIV/AIDS in minority communities.

Congress Examines HIV/AIDS Impact on Hispanic Community

The Congressional Hispanic Caucus, with the Congressional Hispanic Caucus Institute, convenes hearings on the impact of HIV/AIDS on the Latino community.

July 19, 1999
U.S. Funds Program to Address Global Epidemic

President Clinton announces the formation of the “Leadership and Investment in Fighting an Epidemic” Initiative, which will provide funding to address the global HIV epidemic.

AIDS Becomes Number One Killer in Africa

The World Health Organization announces that HIV/AIDS has become the fourth biggest killer worldwide and the number one killer in Africa.

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WHO estimates that 33 million people are living with HIV worldwide, and that 14 million have died of AIDS.

January 10, 2000
UN Addresses AIDS as Global Peace & Security Threat

he United Nations Security Council meets to discuss the impact of AIDS on peace and security in Africa. This marks the first time that the council discusses a health issue as a threat to peace and security.

January 27, 2000
President Clinton Announces Global Vaccine Initiative

In his State of the Union address, President Bill Clinton announces the launch of the Millennium Vaccine Initiative to create incentives for developing and distributing vaccines against HIV, TB, and malaria.

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In his address, President Clinton calls for concerted international action to combat infectious diseases in developing countries.  The President asks for foundations, pharmaceutical companies, international agencies, and other governments to join in this task.


April 30, 2000
President Clinton Declares HIV/AIDS a National Security Threat

President Clinton declares that HIV/AIDS is a threat to U.S. national security.

May 10, 2000
U.S. Begins Importing HIV Treatments to Developing Countries

President Clinton issues an Executive Order to assist developing countries in importing and producing generic HIV treatments.

Global Pressure Results in Reduced Drug Cost for Developing Countries

UNAIDS, the World Health Organization, and other global health groups announce a joint initiative with five major pharmaceutical manufacturers to negotiate reduced prices for HIV/AIDS drugs in developing countries.

July 19, 2000
Stephen Gendin — AIDS Activist Icon — Dies

Stephen Gendin, an AIDS activist and writer who founded a nationally known mail-order prescription service for people infected with HIV, died of AIDS-related illness in New York’s Roosevelt Hospital. He was 34.

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Firmly planted at the center of AIDS activism for 15 years, Gendin is credited for having promoted constructive changes in government policy that would improve the lives of HIV-positive people. His activism was pivotal in reforming the FDA drug approval process to expedite HIV and AIDS patients’ access to more effective anti-retroviral treatments.

He was involved with ACT UP (New York and Rhode Island chapters), Sex Panic!, Community Prescription Service, and the Radical Faeries.  He also wrote a widely read column in POZ magazine. In this column, he shared the toll AIDS took on his body in graphic details and other personal experiences.

“Stephen was a willing guinea pig, his body a non-stop experimental laboratory for new treatment strategies.  His curiosity and courage contributed to what we have all learned about anti-retroviral treatment,” wrote Sean Strub, POZ Magazine’s founder and advisory editor.

Strub said he met Gendin in 1988, shortly after Gendin graduated from Brown University.  In ACT UP/New York, they worked together on the fundraising committee.  In 1990, Strub hired Gendin to work for his company, and for ten years they collaborated on various projects, including fundraising for community non-profits, publishing POZ magazine and launching the Community Prescription Service.

As a co-founder and the chief executive of the Community Prescription Service, Gendin oversaw the organization’s mail-order pharmacy service that distributed medication and information for people with HIV and AIDS, according to the New York Times.

Following Gendin’s death, POZ posted this video tribute to the legendary activist.

July 23, 2000
G8 Summit Leaders Call for Increase in Worldwide Resources for HIV/AIDS

The leaders of the “Group of Eight” (G8) Summit release a statement acknowledging the need for additional HIV/AIDS resources.

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G8 members make up most of the world’s largest economies, and include: Canada, France, Germany, Italy, Japan, Russia, the United Kingdom, and the United States.

August 19, 2000
U.S. Congress Responds to Need for Global Assistance

Congress enacts the Global AIDS and Tuberculosis Relief Act of 2000, which provides assistance to countries with large populations of people living with HIV/AIDS.

UN Adopts Millennium Development Goals to Reverse Spread of HIV

As part of its Millennium Declaration, the United Nations adopts the Millennium Development Goals, which include a specific goal of reversing the spread of HIV/AIDS, malaria, and TB.

September 7, 2000
Congress Reauthorizes Ryan White CARE Act

Congress reauthorizes the Ryan White CARE Act for the second time.

May 18, 2001
HIV Vaccine Awareness Day Observed

May 18 is the first annual observance of HIV Vaccine Awareness Day.

June 25, 2001
UN General Assembly Calls for Global Fund

The United Nations (UN) General Assembly holds its first Special Session on AIDS (UNGASS) and passes the UNGASS Declaration of Commitment and the ILO (International Labor Organization) Code of Practice on HIV/AIDS in the Workplace.

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The meeting also calls for the creation of an international “global fund” to support efforts by countries and organizations to combat the spread of HIV through prevention, care, and treatment, including the purchase of HIV medications.

U.S. Reaffirms HIV/AIDS Is National Security Threat

Newly appointed U.S. Secretary of State, Colin Powell, reaffirms the U.S. statement that HIV/AIDS is a national security threat.

Major Pharma Companies Further Reduce Cost of Therapies

After generic drug manufacturers offer to produce discounted, generic forms of HIV/AIDS drugs for developing countries; several major pharmaceutical manufacturers agree to offer further reduced drug prices to those countries.

HRSA Prioritizes Untreated HIV+ Individuals

The U.S. Health Resources and Services Administration (HRSA) begins focusing on individuals with HIV disease who know their status and are not receiving HIV-related services. HRSA instructs its grantees to address this population’s “unmet need” for services.

CDC Strategic Plan Addresses Major Curtailment in HIV Transmission

The U.S. Centers for Disease Control and Prevention (CDC) announce a new HIV Prevention Strategic Plan to cut annual HIV infections in the U.S. by half within five years.

November 4, 2001
Doha Declaration Announced; Promotes Generics

The World Trade Organization (WTO) announces the Doha Declaration , which affirms the rights of developing countries to buy or manufacture generic medications to meet public health crises such as HIV/AIDS.

January 22, 2002
Global Fund Launched to Fight AIDS, Tuberculosis & Malaria

The Global Fund to Fight AIDS, Tuberculosis and Malaria, a partnership between governments, civil society organizations, the private sector, and affected communities, is established. In April of 2002, The Global Fund approves its first round of grants to governments and private-sector organizations in the developing world. The grants total $600 million for two-year projects.

April 25, 2002
Global Fund Issues 2-year Grants

The Global Fund approves its first round of grants to governments and private-sector organizations in the developing world. The grants total $600 million for two-year projects.

June 25, 2002
Access to Drugs Improved for Poor Countries

The United States announces a framework that will allow poor countries unable to produce pharmaceuticals to gain greater access to drugs needed to combat HIV/AIDS, malaria, and other public health crises.

India, China, Russia, Nigeria & Ethiopia Represent Next Wave of Epidemic

The U.S. National Intelligence Council releases Next Wave of the Epidemic, a report focusing on HIV in India, China, Russia, Nigeria, and Ethiopia.

January 28, 2003
President Bush Announces PEPFAR with $15 Billion in Funding

President George W. Bush announces the creation of the United States President’s Emergency Plan For AIDS Relief (PEPFAR) in his State of the Union address. PEPFAR is a $15 billion, 5-year plan to combat AIDS, primarily in countries with a high burden of infections.

April 18, 2003
CDC Announces New Prevention Initiative

CDC announces Advancing HIV Prevention: New Strategies for a Changing Epidemic, a new prevention initiative that aims to reduce barriers to early diagnosis and increase access to, and utilization of, quality medical care, treatment, and ongoing prevention services for those living with HIV.

December 1, 2003
WHO Announces ‘3 By 5’ Initiative

The World Health Organization (WHO) announces the “3 by 5” initiative , to bring treatment to 3 million people by 2005.

Congress Authorizes $350 Million for PEPFAR

In January, the U.S. Congress authorizes the first $350 million for the United States President’s Emergency Program for AIDS Relief (PEPFAR).

Global Coalition on Women and AIDS is Formed

UNAIDS (the Joint United Nations Programme on AIDS) launches The Global Coalition on Women and AIDS to raise the visibility of the epidemic’s impact on women and girls around the world.

May 27, 2004
FDA Expands Availability of Therapies in Africa and Developing Countries

FDA issues a guidance document for expedited approval of low cost, safe, and effective co-packaged and fixed-dose combination HIV therapies so that high-quality drugs can be made available in Africa and developing countries around the world under PEPFAR.

June 10, 2004
G8 Promotes Global HIV Vaccine Enterprise

Leaders of the “Group of Eight” (G8) Summit (Canada, France, Germany, Italy, Japan, Russia, the United Kingdom, and the United States) call for the creation of a “Global HIV Vaccine Enterprise,” a consortium of government and private-sector groups designed to coordinate and accelerate research efforts to find an effective HIV vaccine.

World Economic Forum Prioritizes HIV/AIDS

During its annual meeting in January, the World Economic Forum approves a set of new priorities, including one with a focus on addressing HIV/AIDS in Africa and other hard-hit regions.

January 26, 2005
FDA Approves Generic Regimen for PEPFAR

The U.S. Food and Drug Administration (FDA) grants tentative approval to a generic copackaged antiretroviral drug regimen for use under the United States President’s Emergency Plan for AIDS Relief (PEPFAR).

June 2, 2005
UN General Assembly Reviews Progress on 2001 Targets

The United Nations (U.N.) General Assembly High-Level Meeting on HIV/AIDS meets to review progress on targets set at the 2001 U.N. General Assembly Special Session on HIV/AIDS (UNGASS).

June 6, 2005
HIV/AIDS in Africa Becomes Focus of G8 Summit

The “Group of Eight” (G8) Summit focuses on development in Africa, including HIV/AIDS. G8 members make up most of the world’s largest economies and include: Canada, France, Germany, Italy, Japan, Russia, the United Kingdom, and the United States.

March 10, 2006
Nat’l Women & Girls HIV/AIDS Awareness Day is Launched

March 10 is the first annual National Women and Girls HIV/AIDS Awareness Day in the U.S.

March 20, 2006
1st National Native HIV/AIDS Awareness Day

March 20 is the first annual observance of National Native HIV/AIDS Awareness Day in the U.S.

May 3, 2006
NIH Sponsors AIDS Conference for Native Americans

On May 3-6, the Office of AIDS Research, in the National Institutes of Health (NIH), sponsors Embracing Our Traditions, Values, and Teachings: Native Peoples of North America HIV/AIDS Conference, in Anchorage, Alaska.

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The conference involves nearly 1,000 participants from the American Indian, Alaska Native, Native Hawaiian, First Nations, and U.S. Territorial Pacific Islander communities.

May 31, 2006
UN Convenes on Declaration of Commitment on HIV/AIDS

The United Nations convenes a follow-up meeting and issues a progress report on the implementation of the Declaration of Commitment on HIV/AIDS .

December 19, 2006
Congress Reauthorizes Ryan White Act for 3rd Time

On December 19, the U.S. Congress reauthorizes the Ryan White CARE Act for the third time.

Bob Hattoy
March 4, 2007
Activist & Clinton Advisor Bob Hattoy Dies

Bob Hattoy, an activist who spoke about AIDS at the 1992 Democratic Convention, dies of AIDS-related illness at UC Davis Medical Center in Sacramento at the age of 56.

[Portrait by Greg Loudon, for an art series for the National Institutes of Health’s National Library of Medicine]

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Hattoy quit his decades-long job as regional director of the Sierra Club in Los Angeles to join Bill Clinton’s presidential campaign during the 1992 primary.  Shortly thereafter, he learned that he had AIDS-related lymphoma and began chemotherapy treatments.  That didn’t stop him from stumping for Clinton in front of AIDS and gay and lesbian communities all over the nation.

Political activist and author David Mixner remembered well Hattoy’s groundbreaking speech to the delegates of the 1992 Democratic Convention, made shortly after receiving his diagnosis.

“The hall was in the usual hubbub that passes for normal even when speeches are going on. But as Bob Hattoy mounted the podium, stillness fell over the entire place,” Mixner recalled.  “One by one, the delegates stood up, until all 5,000 people were on their feet in respect.”

Hattoy then said the opening words of his speech: “This is difficult.”

“There was not a dry eye in the nation that night,” said Mixner.  “Those of us in the hall had black armbands to honor those we knew who had died of ADIS and held onto each other as he spoke.  It was as if at last we were finally being heard after a decade of horror, death and abandonment.”

Jackie McCort of the Sierra Club said of watching her former colleague at the convention: “We gathered around the TV together that night, so thrilled and touched that ‘one of our own’ was speaking so eloquently to the American people.  Doggone, we were proud!”

Beginning in 1993, Hattoy worked in the Clinton administration as a deputy in the White House Office of Personnel.  In the Old Executive Office Building next door to the White House was Hattoy’s office, which he shared with a colleague.  On his desk was a rainbow pride flag and on the walls were photos of he and his boyfriend.

There, he spent most of his days overseeing the search and screening process for potential hires for midlevel posts in agencies like the Interior Department and Environmental Protection Agency.  But Hattoy also saw his role as largely that of internal agitator, checking up almost every day on the progress of issues with more senior officials and sharing those developments with key members of his network.

“I never think of Bob as someone on the White House staff,” said activist Larry Kramer.  “I think of him as our mole.”

In March 1993, when President Clinton said he was considering restrictions on the roles gays and lesbians might be allowed to take in the military, Hattoy compared that to “restricting gays and lesbians to jobs as florists and hairdressers” in civilian life.  This public outburst branded Hattoy as unpredictible and potentially problematic to the Clinton administration.

In a June 1993 wine-fueled interview with The New York Times, Hattoy said, “Basically, I’m an activist first and a White House employee second.  If they fire me, I’ll go to work in a lesbian bakery. But they won’t fire me. We’ve been in too many wars together.”

The next year, to decrease his visibility, the administration appointed him to the position of White House liaison on environmental matters at the Interior Department, where he remained until 1999.  He also served as chairman of the research committee of the Presidential Commission on HIV/AIDS.

“Having been a lobbyist and activist for 20 years, I’d be perfect on the Hill or with community groups or other political coalitions they need to maintain relationships with and keep going — I mean with the progressive community,” Hattoy told POZ magazine in April 1994.  “I originally wanted to do that. That didn’t happen, I think, because — well, I know why.”

“For 25 years, I’ve been an outspoken activist, outspoken about what I’ve believed in and cared about. And for a while that fit perfectly into helping to identify who Bill Clinton was as a human being, to show that he meant it when he talked about how there’s no such thing as Them and Us in America,” he explained.  “When I continued to speak out after the election, it became off-message, I think a lot of people in the White House didn’t know what to do with me.”

A few years after the White House job ended, California Governor Gray Davis appointed him to the California Fish & Game Commisison, which Hattoy promptly joked he would work to rename the “Swish and Fish Commission.”  The post was unpaid and required hundreds of hours of work, with more than a dozen public hearings each year, site inspections, lobbying and other responsibilities.

In the months before his death, he worked on the California Marine Protection Act, creating huge expanses of sea that are like protected state parkland, only underwater.  For environmentalists and preservationists, the legislation was an historic victory, for which Hattoy deserved much of the credit.  Soon after, he was elected Chairman of the commission.

Throughout the years, Hattoy battled recurrent pneumonia and other complications several times and suffered a bone marrow infection a few weeks before his death, but was generally healthy and extremely productive throughout his years with AIDS.

Following Hattoy’s death, former President Bill Clinton and former Secretary of State Hillary Clinton released a joint statement:

“We have lost a pioneer, a leader, and a friend. Bob Hattoy devoted his life to the fight for civil rights and social justice for the gay community and people living with AIDS.  We will always be grateful for his courageous and moving speech at the 1992 Democratic National Convention and afterward, for his years of dedicated service in the administration. He gave hope to a community that feared their voice would never be heard at the highest levels of government.”

May 30, 2007
WHO & UNAIDS Issue Testing Guidelines, Criticism Follows

In an attempt to increase HIV testing, the World Health Organization and UNAIDS recommend “provider-initiated” HIV testing in healthcare settings.

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The WHO/UNAIDS guidelines state that in addition to expanding access to HIV testing, “equal efforts must be made to ensure that a supportive social, policy and legal framework is in place to maximize positive outcomes and minimize potential harms to patients.”  The recommended framework includes social mobilization, health care provider training, a strong monitoring and evaluation system and laws and policies against discrimination based on HIV status, risk behavior or gender.

In a response to the WHO/UNAIDS guidelines, Human Rights Watch pointed out that “few countries have strong legal frameworks in place and enforced, and that in many regions and countries resources are inadequate.”

HRW presented the following facts that could undermine the WHO/UNAIDS guidelines:

  • Worldwide, less than 10% of injecting drug users have access to HIV prevention.
  • About the same percentage of pregnant women living with HIV in Africa has access to the medicine necessary to prevent transmission to their infants.

“The United Nations set a goal of universal access to HIV prevention and treatment by 2010, but currently only an estimated 2 million of the 7 million people living with HIV in urgent need of treatment are receiving it,” HRW stated.

Rwanda Hosts Int’l HIV/AIDS Implementers Meeting

The Rwandan Government hosts the International HIV/AIDS Implementers Meeting, drawing 1,500 delegates to share data and ideas.

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Sharing lessons on HIV prevention, treatment, and care, attendees participate in an open dialogue about future directions of HIV/AIDS programs, with a strong emphasis on implementation and identification of critical barriers and best practices.

A session titled “Making care truly comprehensive and providing a preventive care package for people living with HIV” featured lessons on providing comprehensive care, mostly based on the holistic palliative care model deveopled in Cote d’Ivoire, Rwanda, Tanzania, Zambia and South Africa.  It was noted, however, that none of the speakers mentioned TB prevention, diagnosis and treatment.

“Do not forget about TB!!” urged WHO in its summary of the conference.

A satellite meeting organized by PEPFAR and the Secretariat of the TB/HIV Working Group at WHO was attended by implementers from 22 countries. The main topic of discussion was how PEPFAR funds can be used to support TB control activities.

Cosponsors include WHO; UNAIDS; the U.S. President’s Emergency Plan for AIDS Relief (PEPFAR); The Global Fund to Fight AIDS, Tuberculosis, and Malaria; UNICEF; the World Bank; and GNP+ (the Global Network of People Living with HIV) .

July 7, 2007
Social Justice Leader Ferd Eggan Dies

Ferd Eggan, longtime HIV/AIDS activist and leader of Los Angeles city services, dies at his home in Hollywood at age 60 after a six-month illness complicated by HIV.

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While serving as AIDS Coordinator for the City of Los Angeles between 1993 and 2001, Ferd opened doors for the funding of self-organized programs for women with AIDS, city authorization of and funding for needle exchanges, housing for People With AIDS who might still be active drug users, and a landmark study and intervention program for gay men using crystal meth.

Eggan’s activism began during his college days at the University of Chicago in the 1960s, initially in the southern black civil rights movement and later in anti-war, anti-capitalist, anti-racist, women’s and gay liberation and HIV/AIDS struggles.

“Picture me and a Black GI on leave from Vietnam, in his car in the moonlight, windows steamy, ducking as headlights swept past,” Eggan wrote in his autobiographical essayFags and Dykes Want Everything: Dreaming with the Gay Liberation Front.  “We could be beaten or killed for what we were doing.”

In the years that followed, Eggan traveled between New York City (where he was around the corner from Christopher Street on the first night of the Stonewall riots, but was “too afraid to join in”) and San Francisco.  In 1972, while appearing as an extra in a San Francisco Opera production of Aida, Eggan and two others unfurled a banner from the stage reading, “Dykes and Fags Support the Vietnamese Peace Plan.”

Eggan returned to the Chicago area with his then-partner, documentary filmmaker Carel Rowe, where he soon joined the Chicago chapter of the Gay Liberation Front. He worked for a while with a childcare co-op run by women connected with the “Jane” group, which helped women get underground abortions, and he taught Puerto Rican high school students for 11 years.

Diagnosed with HIV in 1986, Eggan helped to found ACT UP Chicago and the national ACT UP PISD Caucus (People with Immune System Disorders), before moving to Los Angeles in 1990 to become Executive Director of Being Alive.

In 1993, Eggan became the city’s third AIDS coordinator, a position created in 1989 by then-Mayor Tom Bradley to spearhead the development of a comprehensive local approach to combating the spread of AIDS.  He served in this position until 2001, when he became too ill to continue in the job.

After retiring on disability, he concentrated on his creative writing, journalism, video art, and his blog, “Communiques from a Cranky PWA.”  In June 2007, less than three weeks before his death, the Los Angeles City Council honored Eggan for his service.

“We would not be where we are today if it had not been for people like Ferd,” said Dr. Michael Gottlieb, who in 1981 authored the first medical case report that heralded the advent of AIDS. “Part of the founding generation of AIDS activists, he has been involved with AIDS for the life of the epidemic. Even if there were activist leaders waiting in the wings — and regrettably there aren’t — Ferd Eggan would be irreplaceable.”

His long-term friend Walt Senterfit, national board chair of the Community HIV/AIDS Mobilization Project, said, “He was a warrior, strategist, writer, artist, activist, and friend in the political, social, and intellectual movements for liberation of our time.”

CDC Launches ‘Prevention IS Care’ Campaign

In October, the U.S. Centers for Disease Control and Prevention (CDC) launch Prevention IS Care (PIC), a social marketing campaign designed for healthcare providers who deliver care to people living with HIV.

Uganda Hosts HIV/AIDS Implementers Meeting; Activists Arrested

HIV/AIDS implementers from around the world gather in Kampala, Uganda for the 2008 HIV/AIDS Implementers’ Meeting, where three activists were arrested by Ugandan police.

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In recognition of the rapid expansion of HIV/AIDS programs worldwide, the focus of the meeting was building the capacity of local prevention, treatment, and care programs; enhancing quality; and promoting coordination among partners.

A total of 1,700 attendees convened at the meeting, representing governments, nongovernmental organizations including faith- and community-based groups, multilateral organizations, the private sector, and groups of people living with HIV/AIDS.

Cosponsors of the four-day conference include the U.S. President’s Emergency Plan for AIDS Relief (PEPFAR); The Global Fund to Fight AIDS, Tuberculosis, and Malaria; UNAIDS (the Joint United Nations Programme on HIV/AIDS); the World Health Organization (WHO); the United Nations Children’s Fund (UNICEF); the World Bank; and GNP+ (the Global Network of People Living with HIV).

During the conference, three Ugandan LGBT activists were arrested as they protested the statements made by a Ugandan government official who refused to direct funds toward HIV programs that targeted men who have sex with men.

The Uganda Police Force arrested and detained Pepe Julian “Patience” Onziema, Valentine Kalende and Usaam “Auf” Mukwaya — all members of the LGBT organization Sexual Minorities Uganda (SMUG) — when the three activists took the stage at the conference to distribute leaflets and hold up small placards demanding attention to HIV vulnerability among the LGBT community.

The International Gay and Lesbian Human Rights Commission immediately issued a press release condemning the arrests of the activists and calling for their immediate and unconditional release.  The commission expressed concern for the safety of the activists, and noted the Ugandan government routinely discriminated against those speaking up for the LGBT community.

On July 25, a few hours after the activists attended their hearing for their arrest, Kampala police officers abducted one of the activists, Usaam “Auf” Mukwaya, as he returned his hotel.

A patrol car stopped the taxi he was riding in and four men identifying themselves as police officers abducted him and took him to a location where he was held for more than 24 hours without access to a lawyer or any reason provided for his arrest.

Mukwaya told Human Rights Watch that his abductors asked him questions in Luganda, a local dialect, about SMUG’s funders and supporters, and about his own role “among the homosexuals.” They also demanded he give them information about other individuals involved in LGBT rights.

According to Mukwaya, three police officers pushed him through a dark corridor to a room where they sat him on a chair.  Mukwaya reported seeing four other men in the room; they were close to his own age and appeared to have been beaten.  One appeared to have a broken leg.

One of the abductors scraped his knuckles with a razor-like object.  Another tied him to a machine that stretched his arms.  After forcing Mukwaya to strip to his underwear, they asked him if he was a man or a woman, and made him walk around the room unclothed.

The following day, they released him, dropping him on the streets of central Kampala.

Human Rights Watch would issue a statement decrying the treatment of government officials of Mukwaya and noting that “torture and ill-treatment is a pervasive problem” for the LGBT community in Uganda.

July 31, 2008
Bush Reauthorizes PEPFAR, Adjusts HIV Travel Ban

President George W. Bush signs legislation to extend the President’s Emergency Plan for AIDS Relief and loosen the HIV travel ban.

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The legislation budgets $48 billion for PEPFAR to operate an additional five years and also contains a rider that gives the U.S. Department of Health and Human Services the authority to admit HIV-positive travellers to the U.S. on a “case-by-case” basis.

September 18, 2008
National HIV/AIDS and Aging Awareness Day Observed

September 18 is the first observance of National HIV/AIDS and Aging Awareness Day .

September 27, 2008
National Gay Men’s HIV/AIDS Awareness Day Observed

National Gay Men’s HIV/AIDS Awareness Day is first recognized on September 27.

President Obama Calls for National HIV/AIDS Strategy

Newly elected President Barack Obama calls for the development of the first National HIV/AIDS Strategy for the United States.

April 7, 2009
White House & CDC Collaborate on HIV Awareness Campaign

The Obama Administration and the U.S. Centers for Disease Control and Prevention launch the Act Against AIDS campaign.

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The a multiyear Act Against AIDS campaign is designed to reduce HIV incidence in the U.S. through raising awareness about HIV prevention.

The CDC simultaneously launches the Act Against AIDS Leadership Initiative (AAALI) in an effort to increase HIV-related awareness, knowledge, and action within Black communities across the U.S.

May 5, 2009
President Obama Launches $63B Global Health Initiative

President Barack Obama’s Global Health Initiative will develop a comprehensive approach to global healthcare in low- and middle-income countries.

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A six-year, $63 billion effort, the Global Health Initiative received input and involvement from the President’s Emergency Plan for AIDS Relief (PEPFAR).

June 8, 2009
Caribbean American HIV/AIDS Awareness Day Observed

June 8 marks the first annual recognition of Caribbean American HIV/AIDS Awareness Day.

August 17, 2009
Veterans Dept Moves to Increase HIV Testing

The Department of Veterans Affairs moves to increase the number of veterans receiving HIV tests by dropping the requirement for written consent.

October 6, 2009
100th Antiretroviral Drug Approved

The U.S. Food and Drug Administration approves the 100th antiretroviral drug.

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FDA announces that it has approved the 100th antiretroviral drug under the President’s Emergency Plan for AIDS Relief (PEPFAR).  Of the more than 100 products that have received either full or tentative FDA approval under the program, 29 are branded drugs and 71 are generics.

This achievement reflects a five-year-old regulatory process designed to fast-track the delivery of cheap HIV drugs to the developing world through the PEPFAR program.

The FDA process was launched in May 2004, in response to a call from activists, clinicians and members of Congress to use the WHO’s pre-certification drug list to make purchases of generic medications for PEPFAR-funded programs.  Instead, a process was devised to allow the FDA to certify generic antiretrovirals (ARVs) for PEPFAR purchase, even if the branded drug was still protected by U.S. patent laws.

HHS Secretary Kathleen Sebelius said in a statement, “This milestone exemplifies the dedication, caring, and hard work of all who strive to better the lives of those infected with or affected by HIV/AIDS.”

October 28, 2009
Sexual Orientation & Gender Identity Added to Hate Crime Law

President Barack Obama signs into law the Matthew Shepard and James Byrd Jr. Hate Crimes Prevention Act, expanding the 1969 federal hate-crime law to include crimes committed because of a victim’s sexual orientation.

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Named after Matthew Shepard and James Byrd Jr., the measure was conceived as a response to the murders of both men in 1998.

Shepard was a gay college student who was tortured and murdered near Laramie, Wyoming by two men.  Shepard’s murderers were given life sentences — in large part because his parents sought mercy for his killers. Byrd was a 49-year-old disabled Black man from Jasper, Texas who was tied to a truck by three white supremacists, dragged behind it, and decapitated.  Two of Byrd’s murderers were sentenced to death and executed in 2011 and 2019, respectively, while the third was sentenced to life in prison.

“Prosecutors will have new tools to work with states in order to prosecute to the fullest those who would perpetrate such crimes,” President Obama said, “because no one in America should ever be afraid to walk down the street, holding the hands of the person they love.”

The audience at the White House included Matthew Shepard’s parents Denis and Judy, and the family of the late Sen. Edward M. Kennedy, who championed the legislation but died before the bill was passed.

Rules Eased for Needle Exchange Funding

President Barack Obama signs the Consolidated Appropriations Act, which modifies the ban on the use of federal funds for needle exchange programs.

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When applicable, Federal funds may be used for personnel, equipment, syringe disposal services, educational materials, communication and marketing activities and evaluation activities, and evaluation. Some HHS programs may still contain partial or complete bans on the use of funds for needle exchange programs.

January 4, 2010
U.S. Lifts HIV Travel & Immigration Ban

President Barack Obama ends the HIV ban on travel and immigration by removing the remaining regulatory barriers to entry.

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The lifting of the travel ban was done in conjunction with the announcement that the International AIDS Conference would return to the U.S for the first time in more than 20 years.

“If we want to be a global leader in combating H.I.V./AIDS, we need to act like it,” Obama said at a White House ceremony to announce the cancellation of the ban. “Now, we talk about reducing the stigma of this disease, yet we’ve treated a visitor living with it as a threat.”

The Human Rights Campaign, the nation’s largest LGBT civil rights organization, hailed the announcement that the ban, first established in 1987 by the Reagan Administration, has been lifted.  Regulations officially removed HIV from the list of communicable diseases that barred foreign nationals from entering the U.S.

“The United States of America has moved one step closer to helping combat the stigma and ignorance that still too often guides public policy debates around HIV/AIDS,” said HRC President Joe Solmonese.  “Today, a sad chapter in our nation’s response to people with HIV and AIDS has finally come to a close and we are a better nation for it.”

Scientific researchers also applauded the end of the travel ban.

“The removal of the immigration and travel ban on HIV-infected persons was a monumental step in eliminating the exceptionalism of HIV and reducing stigma and social barriers for those living with HIV,” Susanna E. Winston, M.D. and Curt G. Beckwith, M. wrote in their 2011 report in AIDS Patient Care and STDs.

The researchers further called for increased alliances between the U.S. and its immigrant communities as well as additional options for testing.

Not everyone celebrated the end of the HIV travel ban.

“You’re running into a huge public expense because most people simply cannot afford the drugs to treat HIV out of their own pockets,” Ira Mehlman, spokesman for the Federation for American Immigration Reform, told ABC News. “[HIV-positive immigrants] will require all sorts of assistance from the government to pay for the drugs that they need.”

March 23, 2010
Obama Signs ACA, Protections to Those Living With HIV

President Barack Obama signs the Affordable Care Act, providing historic protections for those living with HIV.

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“The Affordable Care Act is one of the most important pieces of legislation in the fight against HIV/AIDS in our history,” according to The Centers for Disease Control and Prevention.

Historically, people living with HIV and AIDS in the U.S. had a difficult time obtaining private health insurance and had been particularly vulnerable to insurance industry abuses.  Consistent with the goals of the Obama Administration’s National HIV/AIDS Strategy, the Affordable Care Act made considerable strides in addressing these concerns and advancing equality for people living with HIV and AIDS.

As of this day, insurers were no longer able to deny coverage to children living with HIV or AIDS.  The parents of as many as 17.6 million children with pre-existing conditions no longer had to worry that their children would be denied coverage because of a pre-existing condition.

Insurers also were prohibited from cancelling or rescinding coverage to adults or children because of a mistake on an application.  And insurers could no longer impose lifetime caps on insurance benefits. Because of the law, 105 million Americans no longer had a lifetime dollar limit on essential health benefits.

These changes to healthcare immediately improved access to insurance for people living with HIV/AIDS and helped people with these conditions retain the coverage they had.


July 13, 2010
1st Comprehensive U.S. HIV/AIDS Strategy Released

The Obama Administration releases the first comprehensive National HIV/AIDS Strategy for the United States.

July 18, 2010
Study of South African Women is Conference Highlight

An important scientific breakthrough for HIV prevention in women garners attention at the International AIDS Conference in Vienna, Austria.

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At the 18th International AIDS Conference on July 18-23, the Centre for the AIDS Programme of Research in South Africa’s (CAPRISA) presented the results of its 004 study of antiretroviral-based microbicides, a vaginal gel that significantly reduces a woman’s risk of being infected by HIV and genital herpes.

The study shows the microbicides to be safe and effective in reducing risks of new HIV infections among women by 39%. Women who use the microbicides as directed have even higher rates of protection (54%) against HIV infection.

The microbicide containing 1% tenofovir — an antiretroviral drug widely used in the treatment of HIV — was considered to have the potential to prevent over half a million new HIV infections in South Africa alone over the next decade.

The study involved 889 women at high risk of HIV infection at an urban and a rural site in KwaZulu-Natal, South Africa. Overall, 98 women out of the 889 became HIV positive during the trial — with 38 in the tenofovir gel group and 60 in the placebo gel group.

Out of the 434 women who tested negative for herpes at the start of the trial, 29 became infected in the tenofovir group and 58 became infected in the placebo group. The reduced rates of HIV and herpes infections among the women who used the tenofovir gel were considered statistically significant.

AIDS United Formed

AIDS Action merges with the National AIDS Fund to form AIDS United

September 20, 2010
UN Summit on Accelerating 2015 Millennium Development Goals

On September 20-22, the United Nations (UN) convenes a summit to accelerate progress toward the 2015 Millennium Development Goals

April 11, 2011
Public Debates Transplant Ban of HIV-Infected Organs

Public debate begins on whether the longstanding ban on transplants of HIV-infected organs should be dropped .

June 8, 2011
Over 3,000 Participate in UN’s High-Level Meeting on HIV/AIDS

Over 3,000 people participate in the United Nation’s (UN) High-Level Meeting on HIV/AIDS in New York from June 8–10.

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The session recognizes critical milestones, including three decades of the pandemic and the 10-year anniversary of the 2001 UN General Assembly Special Session on HIV/AIDS and the resulting Declaration of Commitment . At the Meeting, the U.S. joined with other partners in launching a global plan to eliminate mother-to-child transmission of HIV and keep mothers alive.

July 13, 2011
White House National Strategy Reflects on Year 1 of Program

On the occasion of the one-year anniversary of the White House National HIV/AIDS Strategy, President Obama announces plans to increase efforts to reduce HIV transmission and boost public awareness.

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In a video presentation, President Obama, doctors, researchers, policy makers, community leaders and advocates speak about the one-year-old comprehensive National HIV/AIDS Strategy on the 30th anniversary of the disease.

Federal Agencies Support U.S. National HIV/AIDS Strategy

Lead Federal agencies release implementation plans in support of the U.S. National HIV/AIDS Strategy.

August 7, 2011
U.S. Launches 12 Cities Project to Target High-Infection Areas

The U.S. launches the 12 Cities Project, an initiative to accelerate planning and cross-agency response in areas with high rates of HIV infection.

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Focusing on twelve jurisdictions in the U.S. that bear the highest AIDS burden, the U.S. Department of Health and Human Services rolls out components of the project to cover comprehensive care, treatment and prevention.

Based on an estimate of total AIDS cases reported in December 2007 in cities across the country, HHS selected twelve cities to be included in the initial project.  These cities represent 44% of the total cases in the U.S. in December 2007:

New York City, NY (66,426 cases)
Los Angeles, CA (24,727 cases)
Washington, DC (15,696 cases)
Chicago, IL (14,175 cases)
Atlanta, GA (13,105 cases)
Miami, FL (12,732 cases)
Philadelphia, PA (12,469 cases)
Houston, TX (11,277 cases)
San Francisco, CA (11,026 cases)
Baltimore, MD (10,301 cases)
Dallas, TX (7,993 cases)
San Juan, PR (7,858 cases)

Phase I of this project, from October 2010 to April 2011, focused on data collection and planning, with an explicit focus on identifying gaps in coverage in terms of populations, interventions, and services.  Phase II, from May to September 2011 “and beyond,” focused on responding to the results of the enhanced planning process, including making recommendations about redirecting resources in order to optimize outcomes.

Regional Dialogues Begin on National HIV/AIDS Strategy

In September, the Office of National AIDS Policy begins to convene a series of five regional dialogues to focus attention on critical implementation issues for the National HIV/AIDS Strategy.

Barbara Lee
September 30, 2011
Town Halls Kick Off in Build-up to ‘AIDS 2012’

The “Road to AIDS” town hall comes to San Francisco, the first in a nationwide event series building up to the International AIDS Conference.

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The San Francisco Town Hall brought together diverse community members to talk about where we are with the HIV epidemic 30 years in, and where we’re going.

The first of fifteen town halls across the U.S., San Francisco’s event included U.S. Congresswoman Barbara Lee (shown in photo), as well as participation from panelists Andrew Forsyth, PhD, HHS, Office of the Deputy Assistant Secretary for Health/Infectious Diseases; Grant Colfax, MD, Director of HIV Prevention and Research, San Francisco Department of Public Health; Herb K. Schultz, Regional Director, HHS, Region IX; Charles Fann, Community Co-Chair for the San Francisco HIV Prevention Planning Council and Health Promotions Program Manager at Tenderloin Health; Sharyn Grayson, Co-Chair at Collaborative Community Planning Council – Oakland TGA; Kabir Hypolite, PhD, Director, Office of AIDS Administration, Alameda County; and Marsha A. Martin, DSW, Director, Get Screened Oakland.

Across the panelists’ responses, several themes emerged including the need to:

  • Put patients and communities first
  • Enhance collaboration and breaking down of silos
  • Align resources (especially when they are limited) with the goals of the National HIV/AIDS Strategy by looking at the data
  • Strengthen stakeholder engagement
  • Provide a comprehensive and coordinated system of HIV prevention and care
  • Work across cultural lines

Each of the fifteen “Road to AIDS” town halls was free and open to the public, and took place over the 11 months leading up to “AIDS 2012,” the XIX International AIDS Conference, on July 22-27, 2012 in Washington, DC.

“AIDS 2012” would be the largest gathering of people working in HIV to date.

November 8, 2011
Secretary Clinton Calls for ‘AIDS-Free Generation’

Secretary of State Hillary Rodham Clinton shares the U.S. Government’s new vision of creating an AIDS-free generation.

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Speaking before the National Institutes of Health, Clinton delivered remarks on the future of the global HIV/AIDS epidemic, reflected on the past 30 years of the epidemic, and outlined a vision for turning the tide on HIV/AIDS.

“Our efforts have helped set the stage for a historic opportunity, one that the world has today: to change the course of this pandemic and usher in an AIDS-free generation,” Clinton said.

“Now, by an AIDS-free generation, I mean one where, first, virtually no children are born with the virus; second, as these children become teenagers and adults, they are at far lower risk of becoming infected than they would be today thanks to a wide range of prevention tools; and third, if they do acquire HIV, they have access to treatment that helps prevent them from developing AIDS and passing the virus on to others.”

Clinton’s speech was considered to be the Obama’s administration’s first effort to publicly set an ambitious goal to eradicate the disease.  Following her remarks, administration officials scrambled to suggest ways that the initiative could be funded, including diplomatic pressure on governments in developing countries to spend more of their own money and political pressure on wealthy nations to contribute more.

During her speech, Clinton also introduced comic performer and talkshow host Ellen DeGeneres as a new Special Envoy for Global AIDS Awareness.

Clinton’s full speech is available here.

Dr. Eric Goosby, the Obama administration’s global AIDS coordinator, said this was only the first of several speeches that administration officials planned to make on AIDS in the next few months.

December 1, 2011
Obama Launches Plan to Increase Global Fund Commitments

On December 1 (World AIDS Day), at the ONE Campaign and (RED) event in Washington, DC, President Obama announces accelerated efforts to increase the availability of treatment to people living with HIV/AIDS in the United States.

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He challenges the global community to deliver funds to The Global Fund to Fight AIDS, Tuberculosis and Malaria , and calls on Congress to keep its past commitments intact. He calls on all Americans to keep fighting to end the epidemic.

March 27, 2012
HHS Recommends Treatment For All HIV-Positive People

The U.S. Department of Health and Human Services issues new HIV treatment guidelines recommending treatment for all HIV-infected adults and adolescents, regardless of CD4 count or viral load.

July 16, 2012
Truvada for PrEP Approved

The FDA approves the use of Truvada® for pre-exposure prophylaxis (PrEP). Adults who do not have HIV, but who are at risk for infection, can now take this medication to reduce their risk of getting the virus through sexual activity.

July 22, 2012
International AIDS Conference Returns to the U.S.

The XIX International AIDS Conference (AIDS 2012 ) is held in Washington, DC—the first time since 1990 that the conference has been held in the United States.

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Conference organizers had refused to convene the event in the U.S. until the Federal government lifted the ban on HIV-positive travelers entering the country.

January 1, 2013
PEPFAR Commemorates 10th Anniversary

The U.S. President’s Emergency Plan for AIDS Relief (PEPFAR) celebrates its 10th anniversary.

June 18, 2013
More Than 1 Million Infants Born HIV-Free Due to PEPFAR

Secretary of State John Kerry announces that, thanks to direct PEPFAR support, more than 1 million infants have been born HIV-free since 2003.

July 13, 2013
Obama Executive Order Promotes HIV Care Continuum

President Obama issues an Executive Order directing Federal agencies to prioritize supporting the HIV care continuum as a means of implementing the National HIV/AIDS Strategy.

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The HIV Care Continuum Initiative aims to accelerate efforts to improve the percentage of people living with HIV who move from testing to treatment and—ultimately—to viral suppression.

November 12, 2013
HOPE Act Signed, Allowing Organ Transplants Among HIV-Positive Individuals

President Obama signs the HIV Organ Policy Equity (HOPE) Act, which will allow people living with HIV to receive organs from other infected donors. The HOPE Act has the potential to save the lives of about 1,000 HIV-infected patients with liver and kidney failure annually.

January 1, 2014
ACA Grants Protections Against Pre-Existing Conditions

January 1: Major provisions of the Affordable Care Act designed to protect consumers go into effect. Insurers are now barred from discriminating against customers with pre-existing conditions, and they can no longer impose annual limits on coverage—both key advances for people living with HIV/AIDS.

March 1, 2014
UN Commission Reports Challenges of Implementing MDGs

The United Nations Commission on the Status of Women releases a report on the challenges and achievements of implementing the MDGs for women and girls.

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The Commission concludes that progress on MDG6 (Combating HIV/AIDS, Malaria, and Other Diseases) has been limited, given that the number of women living with HIV globally continues to increase. The report notes several key challenges: adolescent/young women’s particular vulnerability to HIV; the need to increase access to healthcare services; and the challenges of structural gender inequalities, stigma, discrimination, and violence.

March 4, 2014
Dr. Debeorah Birx Becomes U.S. Global AIDS Coordinator

Dr. Deborah Birx is sworn in as Ambassador at Large and U.S. Global AIDS Coordinator to oversee the President’s Emergency Plan for AIDS Relief (PEPFAR). She replaces Dr. Eric Goosby.

March 24, 2014
1st African American & HIV-Positive Person Heads ONAP

Douglas Brooks is appointed as the new Director of the White House Office of National AIDS Policy (ONAP). He is the first African American and the first HIV-positive person to hold the position.

July 20, 2014
AIDS 2014 Draws 14,000 Delegates

Nearly 14,000 delegates attend the 20th International AIDS Conference, travelling to Melbourne, Australia from over 200 nations.

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One key message of the conference is that a one-size-fits-all approach may not be suitable for all settings, especially given the diversity of the epidemic’s geographical hotspots and key populations.

Interventions and policies will require target-based strategies and greater support of key populations, especially in countries where discriminatory policies and legislation are hindering prevention and treatment efforts.

October 9, 2014
CDC Reports Care and Treatment of Latinos Lag

CDC releases a new report that finds gaps in care and treatment among Latinos diagnosed with HIV.

December 23, 2014
FDA Relaxes Ban on Blood Donations From MSM

FDA announces it will recommend changing the blood donor deferral guidelines for men who have sex with men from permanent deferral to one year since the last sexual contact.

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In 1983, the agency imposed a lifetime ban on donating blood for all men who have ever had sex with another man.

February 5, 2015
HHS Project Address HIV Disparities Among MSM of Color

HHS announces the launch of a new, 4-year demonstration project to address HIV disparities among MSM of color. The cross-agency project, “Developing Comprehensive Models of HIV Prevention and Care Services for MSM of Color,” will support community-based models for HIV prevention and treatment.

February 23, 2015
CDC Report Identifies Groups with Disproportionate Levels of HIV

HIV diagnosis rates in the U.S. remain stable between 2009-2013, but men who have sex with men (MSM), young adults, racial/ethnic minorities, and individuals living in the South continue to bear a disproportionate burden of HIV, according to the Center for Disease Control’s 2015 DC’s annual HIV Surveillance Report.

May 8, 2015
HHS Further Loosens Restrictions on Organ Transplants

The U.S. Department of Health and Human Services announces on May 8 that it will amend the Federal rules covering organ transplants to allow the recovery of transplantable organs from HIV-positive donors.

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The new regulations will provide a framework for clinical studies on transplanting organs from HIV-positive donors to HIV-positive recipients.

July 14, 2015
UNAIDS Announce Millennium Development Goal Achieved Early

UNAIDS announces that the targets for Millennium Development Goal #6 —halting and reversing the spread of HIV—have been achieved and exceeded 9 months ahead of the schedule set in 2000.

July 18, 2015
U.S. Agencies Collaborate on Housing Assistance Programs

The U.S. Departments of Housing and Urban Development and Justice announce they will collaborate on a demonstration project to provide housing assistance and supportive services to low-income persons living with HIV/AIDS who are victims of sexual assault, domestic violence, dating violence, or stalking.

July 30, 2015
White House Announces National HIV/AIDS Strategy Update

The White House launches the National HIV/AIDS Strategy: Updated to 2020.

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The updated Strategy retains the vision and goals of the original, but reflects scientific advances, transformations in healthcare access as a result of the Affordable Care Act, and a renewed emphasis on key populations, geographic areas, and practices necessary to end the domestic HIV epidemic.

September 26, 2015
New PEPFAR Targets Released at UN Summit

At a United Nations summit on the Sustainable Development Goals, the United States announces new PEPFAR prevention and treatment targets for 2016–2017.

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By the end of 2017, the U.S. will commit sufficient resources to support antiretroviral therapy for 12.9 million people, provide 13 million male circumcisions for HIV prevention, and reduce HIV incidence by 40% among adolescent girls and young women within the highest burdened areas of 10 sub-Saharan African countries.

September 30, 2015
WHO Announces New Treatment Recommendations

The World Health Organization announces new treatment recommendations that call for all people living with HIV to begin antiretroviral therapy as soon after diagnosis as possible.

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WHO also recommends daily oral PrEP as an additional prevention choice for those at substantial risk for contracting HIV. WHO estimates the new policies could help avert more than 21 million deaths and 28 million new infections by 2030.

October 20, 2015
New Campaign Targets Women at Risk of Violence and HIV

Greater Than AIDS launches a new campaign, Empowered: Women, HIV and Intimate Partner Violence, to bring more attention to issues of relationship violence and provide resources for women who may be at risk of, or dealing with, abuse and HIV.

November 15, 2015
amfAR Institute for HIV Cure Research at UCSF Established

amfAR, The Foundation for AIDS Research, announces its plan to establish the amfAR Institute for HIV Cure Research at the University of California, San Francisco. As the cornerstone of amfAR’s $100 million investment in cure research, the Institute will work to develop the scientific basis for an HIV cure by the end of 2020.

December 1, 2015
White House Releases Federal Action Plan on HIV/AIDS

The White House releases a Federal Action Plan to accompany the updated National HIV/AIDS Strategy. The plan was developed by 10 Federal agencies and the Equal Employment Opportunity Commission and contains 170 action items that the agencies will undertake to achieve the goals of the Strategy.

December 19, 2015
Congress Lifts Restrictions on Needle Exchange Programs

Partly in response to the HIV outbreak in Indiana, which is linked to people injecting drugs, Congress lifts restrictions that prevented states and localities from spending Federal funds for needle exchange programs.

December 21, 2015
FDA Lifts Ban on Blood Donations From MSM

The U.S. Food and Drug Administration announces it will lift its 30-year-old ban on all blood donations by men who have sex with men and institute a policy that allows them to donate blood if they have not had sexual contact with another man in the previous 12 months.

March 29, 2016
HHS Releases Guidelines for Funding Syringe Programs

The U.S. Department of Health and Human Services releases new guidance for state, local, tribal, and territorial health departments that will allow them to request permission to use federal funds to support syringe-services programs (SSPs).

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The funds can now be used to support a comprehensive set of services, but they cannot be used to purchase sterile needles or syringes for illegal drug injection.

June 8, 2016
LGBT Groups Blocked from UN Meeting on AIDS

UN member states convene to adopt a declaration to end AIDS, but activists walk out of the meeting and take to the streets to protest the discrimination against LGBTQ people by 51 Muslim states.

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As member states gather at the three-day UN High-Level Meeting on Ending AIDS, the event is marked by controversy after more than 50 nations block the participation of groups representing LGBT people from the meeting.

One goal of the meeting is to adopt the 2016 U.N. Political Declaration on Ending AIDS — a document that lists steps to end the global epidemic by 2030.  However, the political declaration is viewed as exclusionary, discriminatory and inadequate.

“This political declaration has fatal flaws,” said Maureen Milanga of Health GAP, which protested outside UN Headquarters in New York.  “We welcome the new target of reaching 30 million people by 2020 with lifesaving treatment and the pledge to achieve viral suppression for 90% of people on treatment through scaling up differentiated models of quality care.  But unless dangerous donor funding cuts are reversed, millions will be denied access to medicine.”

The final resolution barely mentions those most at risk for contracting HIV/AIDS: men who have sex with men, sex workers, transgender people and people who inject drugs.

The groups excluded from the meeting are nongovernmental organizations (NGOs).  Egypt wrote a letter on behalf of 51 members of the Organization of Islamic Cooperation, objecting to the participation of 11 groups. The letter did not give any reasons, but it was noted that the excluded groups appear to focus on gay and transgender advocacy.

“Given that transgender people are 49 times more likely to be living with HIV than the general population, their exclusion from the high-level meeting will only impede global progress in combating the HIV/AIDS pandemic,” wrote Samantha Power, U.S. ambassador to the UN, in a letter to General Assembly President Mogens Lykketoft.

June 5, 2017
U.S. Website Updates Name to HIV.gov

The federal government’s website on HIV/AIDS changes its name from AIDS.gov to HIV.gov, reflecting a new focus on HIV management.

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The announcement coincides with the 36th anniversary of the Centers for Disease Control and Prevention’s first report of the initial cases of what would become known as AIDS.

U.S. Department of Health and Human Services made the website name change to reflect major scientific advances transforming a nearly always fatal disease to a condition that can be controlled and prevented from progressing to AIDS.

In its announcement to the public, HHS points out the fact that there were more people living with HIV in the U.S. than people living with AIDS.

In the lead-up to the name change, the U.S. Department of Health and Human Services gathered the following input from community organizations:

  • “NMAC (National Minority AIDS Council) applauds the name change from AIDS.gov to HIV.gov, which honors the past while recognizing the power of words and acknowledging that their meanings change over time… The name change reflects the program’s longstanding and ongoing commitment to listen to the HIV community.”
  • “Changing its name from AIDS.gov to HIV.gov is a reflection of AIDS.gov’s commitment to respond to the changing dynamics of the HIV/AIDS epidemic and an acknowledgement of the many scientific and treatment advances we’ve made in recent years. This name change is consistent with the forward thinking we’ve come to expect and depend on from this site.”
    — Phill Wilson, President and CEO, Black AIDS Institute
  • “The Latino Commission on AIDS welcomes renaming AIDS.gov to HIV.gov to focus on preventing the spread of HIV and reaching people at risk for, and living with, HIV with love and compassion.”
    — Guillermo Chacón, President, Latino Commission on AIDS, and Founder of the Hispanic Health Network

HHS also collected input from its federal partners:

  • Anthony S. Fauci, M.D., Director of the National Institute of Allergy and Infectious Diseases:
    “Much progress has been made in HIV/AIDS research since the disease was first recognized in 1981.  The website AIDS.gov has been a valuable resource for those seeking information about HIV/AIDS, and its name change to HIV.gov appropriately reflects our evolution in transforming the pandemic, even as work remains to bring about an end to HIV.”
  • Laura Cheever, M.D., Sc.M., Associate Administrator of HRSA’s HIV/AIDS Bureau:
    “The shift to HIV.gov is important because the face of the epidemic is changing.  What was once a deadly disease is now a manageable, chronic condition, if there is access to testing, high-quality HIV primary medical care, medication, and essential support services, such as those provided by the Ryan White HIV/AIDS Program.”
  • Jonathan Mermin, M.D., M.P.H., Director of CDC’s National Center for HIV/AIDS, Viral Hepatitis, STD and TB Prevention:
    “The shift to HIV.gov is proactive and inclusive, and it sends a strong, supportive message to the 1.1 million people across America who are living with HIV.  The number of annual HIV infections in the U.S. fell 18% between 2008 and 2014, but progress has not been the same for all communities. HIV.gov will deliver current science, accurate information, and links to effective resources for the people who need them most.”
October 7, 2017
California Reduces Penalties for Non-Disclosure of HIV Status

Gov. Jerry Brown signs a bill decreasing the penalty from a felony to a misdemeanor for knowingly exposing a sexual partner to HIV or donating blood without disclosing the infection.

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The public health community lobbied the governor to support the legislation (Senate Bill 239), because it put an end to laws that discouraged people from getting tested and into treatment.  The new law took a public health approach and recognized the current understanding that with treatment, people with HIV effectively have no risk of sexually transmitting HIV to others.

Prior to this, knowingly exposing a sexual partner to HIV was a felony offense punishable by three to eight years in prison.

“HIV is a public health issue, not a criminal issue,” said Sen. Scott Wiener, co-author of the legislation. “These felonies, which treat HIV differently than all other serious communicable diseases, stigmatize people living with HIV and discourage people from getting tested and into treatment.”

The new law, which took effect January 1, changed this to a misdemeanor, carrying a six-month prison term — the same punishment as knowingly exposing someone to other communicable diseases.

According to Lambda Legal, “If you are living with HIV, you no longer have to live with the threat of felony prosecution as a result of other people’s ignorance or someone’s attempt to harm you through a vindictive prosecution. If you are not living with HIV, you should continue taking responsibility for your sexual health and make appropriate choices regarding the sexual risks you are willing to take. And you can expect that more people living with HIV will be willing to have frank conversations about HIV and other sexual health risks, because they no longer have to fear retribution through the criminal justice system.”

December 4, 2017
Gilead Announces Initiative to Address Epidemic in U.S. South

Gilead Sciences announces the launch of the Commitment to Partnership in Addressing HIV/AIDS in Southern States (COMPASS) Initiative, a 10-year, $100 million commitment to support organizations working to address the HIV/AIDS epidemic in the Southern United States.

January 28, 2018
PEPFAR Turns 15, Celebrates Worldwide Impact

PEPFAR (the President’s Emergency Plan for AIDS Relief) celebrates its 15th anniversary.

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When PEPFAR began in 2003, only 50,000 people in Africa were on lifesaving HIV treatment.  At the time, it was the largest commitment ever by any nation to address a single disease.

PEPFAR has grown to supports over 14 million people on treatment globally.

“Over the past 15 years, PEPFAR has transformed the impossible into the possible by rapidly accelerating access to lifesaving HIV prevention and treatment services,” says Ambassador Deborah L. Birx, M.D., U.S. Global AIDS Coordinator. “We have not only saved more than 14 million mothers, fathers, daughters, and sons, but also accelerated global progress toward ending AIDS as a public health threat.”

In this video, one of PEPFAR’s first treatment recipients, John Robert Engole from Uganda tells his remarkable story of survival thanks to PEPFAR’s lifesaving programs.

G8 Nations Renew Commitment to Global Fund

The “Group of Eight” Summit announcemes new commitments to the Global Fund to Fight AIDS, Tuberculosis and Malaria over the next three years.

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The U.S. alone pledged up to $4.3 billion to the Global Fund, which was created in 2002 to address the AIDS, TB and malaria epidemics, which claimed 4 million lives that year alone, mostly in poor countries.

The Global Fund mobilizes and invests billions of dollars each year to support programs run by local experts in more than 100 countries.  In partnership with governments, civil society, technical agencies, the private sector and people affected by the diseases, the Global Fund seeks to overcome funding barriers.

Following the announcement from the G8, the Bill and Melinda Gates Foundation released a statement supporting the funding commitment.

“There is now a critical test for G8 governments: to follow through on the commitments announced this year, and in previous years, by translating what they have agreed into actual financial outlays that support the efforts of poor countries and communities to overcome poverty and disease,” the foundation said.

In 2018, the Global Fund helped finance the distribution of 131 million insecticide-treated nets to combat malaria, provided anti-tuberculosis treatment for 5.3 million people, supported 18.9 million people on antiretroviral therapy for AIDS, and since its founding saved 32 million lives worldwide.

G8 members make up most of the world’s largest economies and include: Canada, France, Germany, Italy, Japan, Russia, the United Kingdom, and the United States.

June 28, 2018
Online HIV-Prevention Program Targets MSM Aged 18-29

In a Northwestern University study, a novel online HIV-prevention program is shown to reduce sexually transmitted infections by 40%.

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Targeting young men who have sex with men (MSM) between the ages of 18-29, the program, “Keep It Up,” offers video clips, soap operas, and interactive games.  It’s the first online HIV-prevention program to record results of a biological outcome.

A month later, the National Institutes of Health would award Northwestern’s Institute for Sexual and Gender Minority Health and Wellbeing with an $8.8 million grant to put its research into practice.

Keep It Up! continues to build its program.  So far, it has been delivered to over 1,500 young men in several major cities.  The program is preparing to bring KIU! to 44 counties across the U.S., and plans to reach at least 4,000 young men in the next few years.


September 7, 2018
HHS Collects Community Input for Updating HIV/AIDS Policy

Community leaders, frontline workers, individuals living with and at risk for infection, and other members of the community from across the nation provide input to leaders from the Office of HIV/AIDS and Infectious Disease Policy.

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Operating under the U.S. Department of Health and Human Services, the Office of HIV/AIDS and Infectious Disease Policy hosted its first “listening session” at the 2018 U.S. Conference on AIDS in Orlando, Florida.

The call for input was part of the HHS plan to receive ideas on priorities and issues to be addressed as it begins work to update the National HIV/AIDS Strategy and the National Viral Hepatitis Action Plan, both of which are set to expire in 2020.

Joined by colleagues from the HHS Office of HIV/AIDS and Infectious Disease Policy, the listening session was convened at a special event during the U.S. Conference on AIDS.  Among the many comments offered during the session, the HHS staff heard about:

  • The importance of addressing housing, incarceration, and other social determinants of health;
  • The need to be strategic in the scale-up PrEP;
  • Concerns that issues of aging and HIV be addressed;
  • Concerns that adequate funding be provided to enact strategies contained in updated plans;
  • The importance of focusing on HIV and hepatitis disparities if we are to end the epidemics;
  • Expectations that funding and support for programs currently in place will be continued, particularly the Ryan White HIV/AIDS Program; and
  • A desire for new forms of accountability for progress.
November 20, 2018
PrEP Urged for High-Risk Individuals

The U.S. Preventive Services Task Force recommends clinicians to offer PrEP (preexposure prophylaxis) to those at high risk for HIV infection.

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The Task Force gives its “A” recommendation — the strongest endorsement it can give — to PrEP, stating that when taken as prescribed, PrEP is highly effective at preventing HIV among those at high risk, and concluding with “high certainty” that there is a substantial benefit to the target population.  The U.S. Preventive Services Task Force is an independent, volunteer panel of national experts in prevention and evidence-based medicine.

In June 2019, the Task Force would upgrade its draft recommendatin to a “Final Recommendation Statement” and present its supporting evidence in a separate report issued to governmental agencies.

February 5, 2019
President Trump Announces 10-year Goal to End HIV

In his State of the Union address, President Donald J. Trump announces his administration’s goal to end the HIV epidemic in the U.S. by 2030.

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The proposed Ending the HIV Epidemic: A Plan for America will leverage new biomedical prevention and treatment options and data to reduce the number of new HIV infections in the U.S. by 75% in five years and by 90% by 2030, said Brett P. Giroir, M.D., HHS Assistant Secretary for Health.

“In short, we will diagnose all people as early as possible, treat rapidly and effectively, protect those at highest risk, respond to any outbreaks with an overwhelming force, and we’re going to create a public health workforce throughout this country with a specific goal of reducing new diagnoses by 75% within 5 years and 90% within 10,” Giroir said.

Experts on the subject expressed skepticism of the strategy based on the administration’s attitude toward HIV/AIDS thus far.

“This pledge is nothing more than an empty gesture following a series of actions that have ignored the needs of the communities most affected by HIV,” said Scott Schoettes, HIV project director at civil rights group Lambda Legal.

Claiming the Trump administration had left HIV risk groups more exposed, activists pointed to actions including cutting funding for health research, working to roll back healthcare for vulnerable groups and offering support for medical staff who to refuse to treat LGBT+ patients on religious grounds.

“President Trump once again presented a broad strokes narrative that people with HIV and AIDS, including LGBTQ Americans, simply can’t trust,” tweeted Sarah Kate Ellis, chief executive of U.S. LGBT+ advocacy organisation GLAAD.

“The only way our world could end HIV transmissions and prioritize proper treatment and prevention is through an exhaustive, across-the-board investment, but President Trump’s words do not back up his administration’s actions.”

March 18, 2019
CDC Corrects Course as Testing & Treatment Gaps Slow Progress

Of the new HIV infections in the U.S. in 2016, the vast majority — about 80% — were transmitted from the nearly 40% of people with HIV who either did not know they had HIV, or who received a diagnosis but were not receiving HIV care.

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Published on the first day of CDC’s 2019 National HIV Prevention Conference, the Vital Signs report provides the latest data on the impact of undiagnosed and untreated HIV in the U.S.

The report underscores the critical need to expand HIV testing and treatment.  A critical part of the proposed “Ending the HIV Epidemic – A Plan for America,” the proposed initiative would strive to end the HIV epidemic in 10 years by focusing first on the geographic areas with the greatest HIV burden, before expanding to reach all areas of the nation affected by HIV.

WeHo HIV Zero with logo
West Hollywood Launches ‘HIV Zero’ Initiative

The City of West Hollywood launches its “HIV Zero” strategic plan, a commitment to making the city a place where people living with HIV have easy access to comprehensive healthcare and social support services.

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The city’s “HIV Zero” initiative also seeks to ensure no members of the community have an elevated risk for acquiring HIV or encounter discrimination based on HIV status, sexual orientation or gender identity.

The four goals of the initiative are to:

  1. Expand access to healthcare for people living with HIV and people currently at an elevated risk
    for acquiring HIV;
  2. Reduce new HIV infections;
  3. Reduce HIV-related disparities and health inequalities; and
  4. Slow disease progress from HIV to Stage 3 (AIDS).

West Hollywood’s “HIV Zero” strategic plan is primarily focused on Los Angeles County Public Health Department surveillance data related to West Hollywood residents in order to determine the success
in meeting epidemiological benchmarks. However, progress is also informed by data sources that may
expand beyond West Hollywood’s boundaries.

Of the 2014 West Hollywood population of 35,053, more than 2,500 residents were people living with HIV.  Of those HIV-positive in the city, 87% were over 35 years old, 99% were male, and 68% were White.  New HIV diagnoses were concentrated almost exclusively among men who have sex with men.

For men in West Hollywood, the number of diagnosed per 100 (0.4) and living with HIV per 100 (12.9) was extremely high, compared to Los Angeles County, where HIV diagnoses was 0.03 per 100 men and living with HIV was 0.9 per 100.

These disparities help clarify why the West Hollywood HIV Zero Initiative was so critical.

May 9, 2019
Truvada Maker Donates Medication for 11-Year Program

Gilead Sciences, maker the only drug approved to prevent HIV infection, will donate enough Truvada to supply 200,000 patients annually for up to 11 years, U.S. health officials announce.

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Truvada is taken once daily to prevent infection with HIV, a strategy called PrEP (pre-exposure prophylaxis). An estimated one million Americans are at risk for infection and should be taking the medication, but only about 270,000 are doing so.

HIV activists and experts had mixed reactions to the news.  Some pointed out that the corporate donation with a value estimated in the billions of dollars would fill only 20% of the need in the U.S.

Critics say that the high cost of Truvada ($2,000 a month) has been called a major barrier to stemming the spread of HIV among low-income Americans, and it’s part of the reason the AIDS epidemic has persisted for so long.

“If we don’t make it possible for those that need it to have access to it, we will continue to have new infections of a completely preventable virus,” said Jaasiel Chapman, clinical research community educator at the University of Cincinnati.

While most insurers cover treatment with the pill, patients can get stuck with out-of-pocket costs that make the medicine unaffordable.

“If there is any example of the dysfunction in the American pharmaceutical system, it is this case,” says James Krellenstein, a member of ACT UP New York. “We have the most effective tool for ending the HIV epidemic, and one reason we’re unable to scale up is because it costs so [much] unnecessarily.”

Upon announcing the Gilead Sciences donation, Health and Human Services Secretary Alex M. Azar II said,“Securing this commitment is a major step in the Trump Administration’s efforts to use the prevention and treatment tools we have to end the HIV epidemic in America by 2030.”

June 11, 2019
PrEP & HIV Testing Receive ‘Grade A’ Recommendations

An independent, volunteer panel of national experts recommends extensive HIV screening and issues a “Grade A” designation for PrEP treatment.

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In its final recommendation statement, the U.S. Preventive Services Task Force urges clinicians to screen for HIV in everyone aged 15 to 65 years and all pregnant people.  In addition, younger adolescents and older adults at increased risk for HIV should also be screened.

The Task Force additionally recommends that clinicians offer PrEP (pre-exposure prophylaxis) to people at high risk of HIV.

In its report, the Task Force notes that while HIV infection rates have been going down, rates among some groups are on the rise, most notably among young adults.

Created in 1984, the U.S. Preventive Services Task Force is an independent, volunteer panel of national experts in prevention and evidence-based medicine. The Task Force works to improve the health of people nationwide by making evidence-based recommendations about clinical preventive services such as screenings, counseling services, and preventive medications.

The Task Force makes recommendations about the effectiveness of specific preventive care services for patients without obvious related signs or symptoms.  It bases its recommendations on the evidence of both the benefits and harms of the service and an assessment of the balance. The Task Force does not consider the costs of providing a service in this assessment.

October 21, 2019
Presidential Advisory Council Focuses on Hispanic Community

The 65th meeting of the Presidential Advisory Council on HIV/AIDS in Miami, Florida draws focus to the needs of the hispanic community.

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Also at the meeting, PACHA holds sessions and discussions on the response to HIV in the populations of Florida and Puerto Rico.

December 3, 2019
Progress Stalls as New Infection Rate Stabilizes

The dramatic decline in annual HIV infections has stopped and new infections have stabilized in recent years, according to a CDC report.

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The report provides the results of a CDC analysis of HIV trends in America from 2010 to 2016 and shows that after about five years of substantial declines, the number of HIV infections began to level off in 2013 at about 39,000 infections per year.

The data analysis suggests that the number of new HIV infections remained stable from 2013 (38,500) to 2017 (37,500).  However, in 2017, an estimated 85.8% of infections were diagnosed.

The CDC researchers conclude that accelerated efforts to diagnose, treat, and prevent HIV infection are needed in order to achieve the U.S. goal of at least 90% reduction in the number of new HIV infections by 2030.

December 3, 2019
‘Ready-Set-PrEP’ Expands Access to Uninsured Patients

The Ready, Set, PrEP program is launched in the U.S. to provide free HIV-prevention medications to thousands of people lacking adequate health insurance coverage.

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Funded by the Department of Health and Human Service, Ready, Set, PrEP expands access to PrEP medications to those unable to afford it.

HHS estimates the number of people who could benefit from PrEP medications at more than 1 million, but less than one-third of them are taking it as prescribed.   This program is still active; to apply, click here.

December 11, 2019
Ryan White HIV/AIDS Program Reports Successful Outcomes

Clients receiving medical care through the Ryan White HIV/AIDS Program were virally suppressed at a record level – 87% – in 2018, according to a new report.

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In a comprehensive review of federal data, the U.S. Health Resources and Services Administration reported the outcomes of all clients served by RWHAP Parts A–D during from 2014 through 2018.  The report provided a strong level of positive outcomes and a hopeful look at the challenges of reaching certain populations in the U.S.

Among the hardest populations to reach are those living at or below 100% of the federal poverty line (32% of clients), lacking in healthcare coverage (20%) and housing that is temporary or unstable (13%).

Serving more than half a million people each year, the Ryan White HIV/AIDS Program (RWHAP) was created in 1990 and currently is funded annually at more than $2 billion.

HRSA’s Ryan White HIV/AIDS Program is divided into five parts:

  • Part A funds medical and support services to counties/cities that are the most severely affected by the HIV/AIDS epidemic:
  • Part B administers funds for states to improve the quality, availability, and organization of HIV health care and support services, and includes grants for the AIDS Drug Assistance Program:
  • Part C administers funds for community-based organizations to provide comprehensive primary health care and support services in an outpatient setting for people with HIV through Early Intervention Services program grants;
  • Part D administers funds for community-based organizations to provide outpatient, ambulatory, family-centered primary and specialty medical care for women, infants, children and youth with HIV; and
  • Part F funds support clinician training, dental services, and dental provider training, as well as the development of innovative models of care to improve health outcomes and reduce HIV transmission.
April 28, 2020
More Funding Allocated to Programs Serving Black Women

The U.S. HIV/AIDS Bureau expands funding opportunities for service organizations working on stigma reduction, rapid ART initiation, and treatment for HIV-positive black women.

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The HIV/AIDS Bureau, which operates under the U.S. Health Resources and Services Administration, announces five Notices of Funding Opportunity (NOFOs) for HIV programs. All five NOFOs are supported by the Minority HIV/AIDS Fund and advance the goals of the Ending the HIV Epidemic (EHE) initiative.

August 17, 2020
HIV Data Dashboard Created to Chart Local Progress

The HIV Data Dashboard is launched to provide a clearinghouse of national and local data, allowing stakeholders at all levels to track progress toward meeting goals to reduce HIV transmission.

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Created by the Health and Human Services Department, AHEAD: America’s HIV Epidemic Analysis Dashboard supports the tracking of goals related to the six indicators for the Ending the HIV Epidemic (EHE) initiative:

  • Reduction of new HIV infections in the U.S. by 75% by 2025 and by 90% by 2030;
  • Demonstration of the historical movement towards achieving the overall goals of the EHE initiative;
  • Diagnosis (number of people with HIV diagnosed in a given year confirmed by laboratory or clinical evidence);
  • Linkage to HIV medical care (percentage of people diagnosed with HIV in a given year who have received medical care for their HIV infection within one month of diagnosis.);
  • Viral suppression (percentage of people living with diagnosed HIV infection who have an amount of HIV that is less than 200 copies per milliliter of blood, in a given year); and
  • PrEP coverage (estimated percentage of individuals prescribed PrEP among those who need it).

You can see how Los Angeles County (and other jurisdictions) are doing toward meetings its goals for 2025 and 2030 by clicking here.

January 1, 2021
ACA Takes Effect; Protections Enacted Against Pre-Existing Conditions

Major consumer protections in the Affordable Care Act (ACA) go into effect, including key advances for people living with HIV/AIDS.

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Healthcare insurance companies are now barred from discriminating against customers with pre-existing conditions, and they can no longer impose annual limits on coverage.

January 15, 2021
U.S. Sets 10-Year Goal to End Epidemic

The U.S. launches The HIV National Strategic Plan for the United States: A Roadmap to End the Epidemic 2021-2025, charting a 10-year plan for reducing new HIV infections by 90% by 2030.

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The Health and Human Services Department releases its HIV Plan, which sets four goals, along with objectives and strategies for use by all partners and stakeholders:

  • Prevent new HIV infections;
  • Improve HIV-related health outcomes of people with HIV;
  • Reduce HIV-related disparities and health inequities; and
  • Achieve integrated, coordinated efforts that address the HIV epidemic among all partners and stakeholders.

According to HHS, its HIV Plan is designed to complement the Center for Disease Control’s Ending the HIV Epidemic in the U.S. (EHE) initiative, with the EHE initiative serving as a leading component of the work by HHS to implement the HIV Plan.

While the EHE initiative is being launched in jurisdictions hardest hit by the epidemic, the HIV
Plan is designed to cover all of the U.S. and has a broader focus across federal departments and agencies beyond HHS and all sectors of society.

March 8, 2021
PACHA Tackles the Intersection of COVID-19 and HIV

The Presidential Advisory Council on HIV/AIDS holds its 70th meeting to discuss, among other things, the intersection of COVID-19 and HIV.

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Other topics addressed at PACHA’s meeting, include the status of the Ending the HIV Epidemic in the U.S. (EHE) initiative and HIV National Strategic Plan, future implementation efforts, and how to better address the needs of women with HIV and of the HIV community.

Formed by President Bill Clinton in 1995 (with each president since renewing the council’s charter) PACHA provides advice, information, and recommendations to the Secretary of Health & Human Services regarding programs, policies, and research to promote effective treatment, prevention and cure of HIV disease and AIDS.

May 12, 2021
CDC Reaffirms Role of STD Clinics in HIV Diagnosis

Underscoring the key role that STD clinics play in HIV diagnosis, prevention, care, and treatment, the Centers for Disease Control re-states its commitment to supporting STD clinics with more than $14 million in funding.

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In a report, the CDC champions the role that STD clinics play in HIV diagnosis, prevention, care, and treatment.  As part of the Ending the HIV Epidemic in the U.S. (EHE) initiative, the CDC releases 43 mllion in funding in August 2020 for seven jurisdictions, including:

  • Alabama Department of Public Health (Jefferson County)
  • Arizona Department of Health Services (Maricopa County)
  • Baltimore City Health Department
  • District of Columbia Department of Health
  • San Francisco Department of Public Health
  • City of Philadelphia Department of Public Health
  • Missouri Department of Health and Senior Services (St. Louis County)

In August 2021, the CDC would go on to create a five-year funding stream of an additional $11.1 million for 11 more EHE juridictions:

  • California Department of Public Health (Sacramento, San Diego, and Orange County)
  • New York City Department of Health and Mental Hygiene
  • Chicago Department of Public Health
  • Florida Department of Health (Orange County)
  • Georgia Department of Public Health (Fulton County)
  • Houston Health Department
  • Indiana State Department of Health (Marion County)
  • Louisiana Department of Health (East Baton Rouge Parish)
  • Maryland Department of Health (Montgomery and Prince George’s County)
  • New Jersey Department of Health (Essex County (Newark))
  • Ohio Department of Health (Franklin County)
  • Texas Department of State Health Services (Dallas County)
June 5, 2021
CDC’s Initial Report of AIDS Turns 40

The world marks 40 years since the first five cases of what later became known as AIDS were officially reported in Los Angeles.

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President Joe Biden, HHS Secretary Xavier Becerra, and Secretary of State Antony J. Blinken release messages recognizing the 40th anniversary. Other events and activities are held across the country to remember the lives that were cut short by this terrible disease and celebrate the resilience and dignity of the more than 38 million people with HIV worldwide.

On this day, the Foundation for The AIDS Monument held its ceremonial groundbreaking at the future site of STORIES: The AIDS Monument in West Hollywood Park.  Among the community members who attend the event is Dr. Michael Gottlieb, one of the authors of the June 1981 CDC report announcing the first five cases of an illness subsequently defined as acquired immunodeficiency syndrome (AIDS).

The five men described in the report were between the ages of 29-36 and resided in the Los Angeles area, and by the time the report was published, two had already died.  The relatively brief report gave scant information about this new medical phenomenon, including the following:

  • The patients did not know each other and had no known common contacts or knowledge of sexual partners who had had similar illnesses.
  • Two of the five reported having frequent homosexual contacts with various partners.
  • All five reported using inhalant drugs, and one reported parenteral drug use (i.e., injected or implanted drugs).
July 22, 2021
‘HIV Challenge’ Spotlights Needs of Racial & Ethnic Minority Communities

HHS announces the launch of The HIV Challenge, a national competition to engage communities to reduce HIV-related stigma and increase prevention and treatment among racial and ethnic minority people.

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Through this challenge, HHS seeks innovative and effective approaches to increase the use of PrEP and ART among people who are at increased risk for HIV or are people living with HIV.

Giving both pre-exposure prophylaxis (PrEP) and antiretroviral therapy (ART) to heterosexual couples where one partner has HIV can almost eliminate the chance of infection in the HIV-negative partner, a study presented at the 2015 Conference on Retroviruses and Opportunistic Infections (CROI 2015) in Seattle shows.


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