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Remembering Sean Sasser

AIDS activist spent final year in D.C.; memorial is Saturday

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Sean Sasser, Real World, RIS, gay news, Washington Blade

Sean Sasser working as a pastry chef at RIS, his last job. Sasser died Aug. 7. (Washington Blade file photo by Michael Key)

Sean Sasser memorial service

Saturday at 11 a.m.

National City Christian Church

5 Thomas Circle, N.W.

seansasserfund.aidsunited.org

Michael Kaplan and his late partner Sean Sasser had a circuitous romantic life.

The two met in 1991 and worked together waiting tables at the same bar in Minneapolis. But both were dating other people at the time and several months later, Sasser moved to San Francisco, a move that would prove life altering. While there, he met, dated and eventually married Pedro Zamora, a romance memorably captured on MTV’s “Real World: San Francisco” during its third season in 1994.

Kaplan and Sasser met again in 1996 at a conference and dated for about two years, some of which was long distance. They were apart for several years but reconnected in 2006 and spent the last six years living together.

Sasser, a long-time AIDS activist and pastry chef, spent his final years in Washington with Kaplan. He died Aug. 7 of HIV-exacerbated mesothelioma, a rare lung cancer Kaplan says Sasser was likely exposed to while working with asbestos fixing up old houses in his native Detroit decades ago. Sasser, born Oct. 25, 1968, was 45.

A public memorial service is planned for Saturday at 11 a.m. at National City Christian Church at Thomas Circle in Washington. “Real World” cast members Judd Winick and Pam Ling will speak along with Phill Wilson, president and CEO of the Black AIDS Institute, and Douglas Brooks, chair of AIDS United’s Board of Trustees and a member of the President’s Advisory Council on HIV/AIDS.

Kaplan is the president and CEO of AIDS United. He spoke with the Blade at length this week about his relationship with Sasser.

After many years of working various jobs and each being in different cities at different times, Kaplan and Sasser moved to Washington last fall. Alarmed by a health scare in May, the two got married in June. Kaplan says it was a “long-term, committed serious relationship” in which “we both talked about and planned our futures together.” At one point in Oregon, the two were foster parents of a child named Alice who lived with them from the time she was 4 to 6.

Sasser had lived with HIV for 25 years; Kaplan for 20. Kaplan says Sasser “went quickly.”

“He probably lost 60 pounds in the last nine weeks of his life,” Kaplan says. “He was a real solid guy. On June 17, they confirmed that this thing in his lung was cancerous. By July, it was confirmed as stage four mesothelioma. He had one round of chemo, but it was just too aggressive. Doctors said he wasn’t strong enough for another round. And by Aug. 7 he was gone.”

Kaplan says he has “a strong network of friends” and is doing as well as can be expected.

“It’s a lot of change right now,” he says.

Sasser is survived by his mother, Pat Robinson Sasser, and a sister, Staci White. Both are expected to attend the service this weekend. Sasser’s father died a few years ago.

After Zamora’s death in November 1994 — just hours after the last episode of his season of “Real World” aired — Sasser, who’d been rejected by the Navy for an HIV-positive test, traveled widely speaking at colleges about HIV. He worked with Health Initiatives for Youth, GLAAD, Human Rights Campaign and the AIDS Alliance for Children Youth & Families. He was appointed by President Clinton to the Presidential Advisory Council on HIV/AIDS.

Kaplan says after about four years of AIDS advocacy work, Sasser was ready to return to his first love — cooking.

He says Sasser never mentioned to people he met that he’d been on “Real World,” but would confirm it if people recognized him and brought it up themselves. He had a few boxes of “Real World” mementos and a couple photos with President Clinton packed away. He took them with him each time he moved, but never unpacked them.

“He didn’t hide it, but he’d moved on,” Kaplan says. “In Portland especially, he’d really built up quite a place for himself as a pastry chef at a hotel there, The Nines. They had two restaurants and he oversaw a lot of banquets and that type of thing there. … He loved the precision of baking and training others how to do it.”

The topic of Zamora wasn’t taboo among them, Kaplan says, and Zamora’s name would come up occasionally. Kaplan recalls watching the 2008 biopic “Pedro” with Sasser and remembers him saying how “hard it is to see someone else portray you” (DaJuan Johnson played Sasser in the film).

Although Kaplan says Sasser would have been shocked that so many media outlets reported his death, he says Sasser “was quite aware of the visibility” his “Real World” appearances had afforded him.

“He definitely knew that it was a real landmark for this young, gay couple, two men of color with HIV, to be shown getting married,” Kaplan says. “For so many people, it was some of the first public faces of HIV they’d seen. They were the first face of many things as young, queer men of color. Sean totally understood the magnitude of that and never shunned it. He didn’t seek attention, but he knew that if having his face out there would make a difference, he was happy to do so.”

Kaplan says one thing that might surprise people about Sasser was his love of children. He mentored several kids affected by HIV in both Portland and Atlanta.

“If Sean had had his way, we would have had three kids and a house,” Kaplan says. “He loved music, he loved baking, he loved traveling and he loved children. He was an incredibly humble person and he was just all about living his life.”

Donations to the Sean Sasser Endowment Fund can be made at seansasserfund.aidsunited.org.

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Puerto Rico

The ‘X’ returns to court

1st Circuit hears case over legal recognition of nonbinary Puerto Ricans

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(Photo by Sergei Gnatuk via Bigstock)

Eight months ago, I wrote about this issue at a time when it had not yet reached the judicial level it faces today. Back then, the conversation moved through administrative decisions, public debate, and political resistance. It was unresolved, but it had not yet reached this point.

That has now changed.

Lambda Legal appeared before the 1st U.S. Court of Appeals in Boston, urging the court to uphold a lower court ruling that requires the government of Puerto Rico to issue birth certificates that accurately reflect the identities of nonbinary individuals. The appeal follows a district court decision that found the denial of such recognition to be a violation of the U.S. Constitution.

This marks a turning point. The issue is no longer theoretical. A court has already determined that unequal treatment exists.

The argument presented by the plaintiffs is grounded in Puerto Rico’s own legal framework. Identity birth certificates are not static historical records. They are functional documents used in everyday life. They are required to access employment, education, and essential services. Their purpose is practical, not symbolic.

Within that framework, the exclusion of nonbinary individuals does not stem from a legal limitation. Puerto Rico already allows gender marker corrections on birth certificates for transgender individuals under the precedent established in Arroyo Gonzalez v. Rosselló Nevares. In addition, the current Civil Code recognizes the existence of identity documents that reflect a person’s lived identity beyond the original birth record.

The issue lies in how the law is applied.

Recognition is granted within specific categories, while those who do not identify within that binary structure remain excluded. That exclusion is now at the center of this case.

Lambda Legal’s position is straightforward. Requiring individuals to carry documents that do not reflect who they are forces them into misrepresentation in essential aspects of daily life. This creates practical barriers, exposes them to scrutiny, and places them in a constant state of vulnerability.

The plaintiffs, who were born in Puerto Rico, have made clear that access to accurate identification is not symbolic. It is a basic condition for moving through the world without contradiction imposed by the state.

The fact that this case is now being addressed in the federal court system adds another layer of significance. This is not a pending policy discussion or a legislative proposal. It is a constitutional question. The analysis is not about political preference, but about rights and equal protection under the law.

This case does not exist in isolation.

It unfolds within a broader context in which debates over identity and rights have increasingly been shaped by the growing influence of conservative perspectives in public policy, both in the United States and in Puerto Rico. At the local level, this influence has been reflected in legislative discussions where religious arguments have begun to intersect with decisions that should be grounded in constitutional principles. That intersection creates tension around the separation of church and state and has direct consequences for access to rights.

Recognizing this context is not an attack on faith or religious practice. It is an acknowledgment that when certain perspectives move into the realm of public authority, they can shape outcomes that affect specific communities.

From within Puerto Rico, this is not a distant debate. It is a lived reality. It is present in the difficulty of presenting identification that does not match one’s identity, and in the consequences that follow in workplaces, schools, and government spaces.

The progression of this case introduces the possibility of change within the applicable legal framework. Not because it resolves every tension surrounding the issue, but because it establishes a legal examination of a practice that has long operated under exclusion.

Eight months ago, the conversation centered on ongoing developments. Today, there is already a judicial finding that identifies a violation of rights. What remains is whether that finding will be upheld on appeal.

That process does not guarantee an immediate outcome, but it shifts the ground.

The debate is no longer theoretical.

It is now before the courts.

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National

LGBTQ community explores arming up during heated political times

Interest in gun ownership has increased since Donald Trump returned to office

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Gun rights organizations and advocates say interest in gun ownership seems to have increased in the LGBTQIA+ community since President Donald Trump returned to the White House last year. (Photo by Kaitlin Newman for the Baltimore Banner)

By JOHN-JOHN WILLIAMS IV | As the child of a father who hunted, Vera Snively shied away from firearms, influenced by her mother’s aversion to guns.

Now, the 18-year-old Westminster electrician goes to the shooting range at least once a month. She owns a rifle and a shotgun, and plans to get a handgun when she turns 21.

“I want to be able to defend my community, especially being in political spaces and queer spaces,” said Snively, a trans woman. “It’s just having that extra line of safety, having that extra peace of mind would be important to me.”

Snively is among what some say is a growing number of LGBTQ gun owners across the United States. Gun rights organizations and advocates say interest in gun ownership appears to have increased in that community since President Donald Trump returned to the White House last year.

The rest of this article can be read on the Baltimore Banner’s website.

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Tennessee

Tenn. lawmakers pass transgender “watch list” bill

State Senate to consider measure on Wednesday

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Tennessee, gay news, Washington Blade
Image of the transgender flag with the Tennessee flag in the shape of the state over it. (Image public domain)

The Tennessee House of Representatives passed a bill last week to create a transgender “watch list” that also pushes detransition medical treatment. The state Senate will consider it on Wednesday.

House Bill 754/State Bill 676 has been deemed “ugly” by LGBTQ advocates and criticized by healthcare information litigators as a major privacy concern.

The bill would require “gender clinics accepting funds from this state to perform gender transition procedures to also perform detransition procedures; requires insurance entities providing coverage of gender transition procedures to also cover detransition procedures; requires certain gender clinics and insurance entities to report information regarding detransition procedures to the department of health.”

It would require that any gender-affirming care-providing clinics share the date, age, and sex of patients; any drugs prescribed (dosage, frequency, duration, and method administered); the state and county; the name, contact information, and medical specialty of the healthcare professional who prescribed the treatment; and any past medical history related to “neurological, behavioral, or mental health conditions.” It would also mandate additional information if surgical intervention is prescribed, including details on which healthcare professional made a referral and when.

HB 0754 would also require the state to produce a “comprehensive annual statistical report,” with all collected data shared with the heads of the legislature and the legislative librarian, and eventually published online for public access.

The bill also reframes detransitioning as a major focus of gender-affirming healthcare — despite studies showing that the number of trans people who detransition is statistically quite low, around 13 percent, and is often the result of external pressures (such as discrimination or family) rather than an issue with their gender identity.

This legislation stands in sharp contrast to federal protections restricting what healthcare information can be shared. In 1996, Congress passed the Health Insurance Portability and Accountability Act, or HIPAA, requiring protections for all “individually identifiable health information,” including medical records, conversations, billing information, and other patient data.

Margaret Riley, professor of law, public health sciences, and public policy at the University of Virginia, has written about similar efforts at the federal level, noting the Trump-Vance administration’s push to subpoena multiple hospitals’ records of gender-affirming care for trans patients despite no claims — or proof — that a crime was committed.

It has “sown fear and concern, both among people whose information is sought and among the doctors and other providers who offer such care. Some health providers have reportedly decided to no longer provide gender-affirming care to minors as a result of the inquiries, even in states where that care is legal.” She wrote in an article on the Conversation, where she goes further, pointing out that the push, mostly from conservative members of the government, are pushing extracting this private information “while giving no inkling of any alleged crimes that may have been committed.”

State Rep. Jeremy Faison (R-Cosby), the bill’s sponsor, said in a press conference two weeks ago that he has met dozens of individuals who sought to transition genders and ultimately detransitioned. In committee, an individual testified in support of the bill, claiming that while insurance paid for gender-affirming care, detransition care was not covered.

“I believe that we as a society are going to look back on this time that really burst out in 2014 and think, ‘Dear God, What were we thinking? This was as dumb as frontal lobotomies,’” Faison said of gender-affirming care. “I think we’re going to look back on society one day and think that.”

Jennifer Levi, GLAD Law’s senior director of Transgender and Queer Rights, shared with PBS last year that legislation like this changes the entire concept of HIPAA rights for trans Americans in ways that are invasive and unnecessary.

“It turns doctor-patient confidentiality into government surveillance,” Levi said, later emphasizing this will cause fewer people to seek out the care that they need. “It’s chilling.”

The Washington Blade reached out to the American Civil Liberties Union of Tennessee, which shared this statement from Executive Director Miriam Nemeth:

“HB 754/SB 676 continues the ugly legacy of Tennessee legislators’ attacks on the lives of transgender Tennesseans. Most Tennesseans, regardless of political views, oppose government databases tracking medical decisions made between patients and their doctors. The same should be true here. The state does not threaten to end the livelihood of doctors and fine them $150,000 for safeguarding the sensitive information of people with diabetes, depression, cancer, or other conditions. Trans people and intersex people deserve the same safety, privacy, and equal treatment under the law as everyone else.”

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