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Hit by HIV, black women reach in to cope, out to empower

Fellowship Story Showcase

Hit by HIV, black women reach in to cope, out to empower

Picture of Jan Jarvis

Reporter Jan Jarvis looks at how black women are dealing with HIV in their community.

Star Telegram
Saturday, August 9, 2008

Every Tuesday, the Chosen Ladies of Distinction, as they call themselves, meet for a fast-food lunch. The Ladies represent the face of HIV in America today. All of the women are members of the Sista to Sista support group at the AIDS Outreach Center in Fort Worth, Texas. The support group is open to all women, yet all of its members are black.

HIV is not just the scourge of big cities such as San Francisco, New York and Chicago. Seven of the 10 states with the highest rate of HIV cases are in the South, where it's ravaging African-Americans, particularly black women, who account for about two-thirds of the 127,000 women with HIV nationwide.

Overall, blacks make up 13 percent of the U.S. population, yet they account for nearly half of the more than 1 million Americans with HIV. AIDS workers say there are myriad reasons for the rise of HIV/AIDS cases among black women.

But the shortage of single black men, a lack of self-esteem and, in some cases, drug addiction play prominent roles.

"There's the typical stuff - racism, low education and poverty - that makes them vulnerable," says Vera Owens, a minister with the Minority AIDS Project in Los Angeles, the first community-based AIDS organization established by blacks. "But really what is happening doesn't have anything to do with race."

Black women are so used to being caregivers that they don't know how to take care of themselves, she says. That's why the L.A. program focuses on building self-worth in girls, before they reach high school.

"We're trying to teach them that their needs are just as important as his needs," she says.

It's a lesson that the Ladies of Distinction - an eclectic blend of 30-somethings juggling jobs and families, and grandmas on disability - are still trying to learn. With their floral sundresses and matching hoop earrigs, the younger Ladies look as if they're ready to go out on a date. The grandmothers of the group may be more inclined to wear sweats, but they're just as feisty when it comes to conversations on everything from the latest hairstyles to men gone bad.

While in their teens and early 20s, many of the Ladies say they never gave HIV a second though; it was a gay white man’s disease. They didn’t use condoms when they had sex. Some were with longtime partners who were intravenous-drug users. Others had sex with strangers. Some got lost in a world of alcohol, drugs and mental illness.

AIDS workers say protection is not a top priority for many of the people they see getting tested.

“If you have $20 in your pocket, are you going to spend it on entertainment or a box of condoms?” asks Daphne Myles, executive director of the Tarrant County AIDS Interfaith Network in Fort Worth. “For a lot of people, condoms are at the bottom of their list.”

Nationwide, 80 percent of women with HIV were infected by having sex with men.

In 2003, 61 percent of high school student reported being sexually active, compared with 43 percent of whites, according to Advocates for Youth, a Washington, D.C, advocacy group. Among black teens, 16 percent reported four or more partners. One study found that nearly one-fourth of teenage black girls said their first sexual experience was with an older man.

Exacerbating the issue is the way young girls are perceived in pop culture, says Carla Stokes, an AIDS activist and founder of Helping Our Teen Girls in Real Life Situations (HOTGIRLS), a nonprofit organization dedicated to improving the health and lives of young black women.

They are often viewed as sexual objects, especially at an early age, she says.

What really matters is not how many sexual partners someone has but what is going to happen to the black community 50 years form now if nothing changes, says Jasmine Burnett, development associate for the Black AIDS Institute in Los Angels

“The world we live in is the world today, not the world we want it to be,” she says. “We have to deal with the problems today based on what people do. We have to meet people where they are.

“What we need is to teach people to be empowered.”

The support group at the AIDS Outreach Center has given the Ladies a safe place to learn how to stand up for themselves and build on their fragile egos.

“Before this support group, I was really depressed,” says Karen, Who has struggled to protect her family from the stigma of her diagnosis. “I felt ugly because of this disease.”

Sharon, who was eight months pregnant when she was diagnosed with HIV, says that every day of her life, she worries about how HIV affects her four children, who have all tested negative.  Her anger and terror show in how quickly she cries when she talks bout long-forgotten dream of being a model.

“HIV has shattered my life,” she says.

Veronica, 36 sees how desperate so many women are to find love, but she urges the group members to shift their attention to themselves.
“We have go to learn to love ourselves,” she says.

Prison’s revolving door

Much has been made about black women becoming infected because of sexual relationships with gay or bisexual men living on the “down low,” or masking their sexual identities by having sexual relationships with women.

But through 2003 estimates linked only 3 percent of AIDS cases among black women to bisexual men.

Instead, AIDS workers point to the high numbers of black men, especially in the South, combined with a high mortality rate due to homicide, disease and other factors, is a contributing factor to HIV among black women, Stokes says.  This unbalanced sex ration has left young black women at a disadvantage.

One of the most outspoken AIDS advocates in Tarrant County was Lady Hoga, who died in 2007. A black woman, Hogan talked about how she was infected by her husband of 17 years, who had been in and out of prison.

He never admitted that he had the disease that killed him in 1995. She was 38 and the mother of three when she tested positive.

In 2005, the state began testing offenders upon their release.  Last year, testing at arrival became required.  The combined data is expected to paint a more accurate picture of how many prisoners are being infected while in prison.

“It’s not that all African-American men are messing around in prison, but a great majority are,” says Jerry Wyatt who had HIV when he began serving a five-year sentence on drug charges in 1995. “I’ve seen it happen with all races.”

Society wants to pretend that it’s not happening, but it’s a part of human sexuality, Owens said.

“You have men coming out of prison who had sex with men and they’re not really gay, they’re just taking care of their sexual needs,” Owens said.  “He’s not going to practice homosexuality when he gets out of prison; he’s coming home to his wife.”

Right now, 80 percent of the positive test are at the time of intake, says Dr. Michael Kelley, director of Preventive Medicine for the Teas Department of Criminal Justice.

The human rights organization Stop Prison Rape found that HIV is four times more common in prisons than on the outside.  Prisoners with HIV have access to treatment, but only about 65 percent of inmates take medication.

They often refuse because everyone will know they are positive and they’ll be targeted by others, says Jeffrey Green, a public health official who works with inmates when they are released.

“Most heterosexuals are not honest about having ex with men while they are in prison,” Wyatt says.  “It’s hard to confess to a spouse, and African-American men especially have a real problem admitting it.”

Living with HIV

But society heaps it on.  The sigma of HIV silenced Sharon for years. Like others, she lives in feat that her children might be ostracized.

Although many of the Ladies have jobs, they fear that they will be persecuted if their employers find out.

People don’t want their employer to know they have HIV,” says Shannon Hilgart, associate executive director of the AIDS Outreach Center.

The stigma of AIDS has left the nation with a generation that would rather die from the disease than admit they have it, Burnett says.

From 1985 to 2004, there were 225,000 AIDS deaths among whites. But blacks, despite being a much smaller group, were close behind with 196 deaths.

Today far fewer are dying, largely because of some 30 medications that are used to treat the virus, says Dr. Elvin Adams, Tarant County Public Health’s medical director.

“In Tarrant County, there are less than 10 deaths a year,” he says.

Most people take one to four pills daily, which costs $1,500 to $2,000 a month when there’s no insurance or federal aid.  TO be eligible for assistance, an individual must be living below the federal poverty level.

A growing number of people get by without taking any HIV medications.

As long as her T cell count stays above 330, Veronica says, she doesn’t have to take any medications and is trying to avoid them.  But recently, when her T cell count plunged, she did some soul-searching.

“I put a brave face on and I was saying I was all right,” she says, “but those things are not what was in my head.”

Many people with HIV try to avoid taking medications, either because they have no health insurance or they fear the side effects.

The medications are easier to live with, but keeping up with the schedule is challenging, Myles says.  

Missing just one pill is risky it gives the virus time to multiply and become resistant to the drugs, Adams says.

Think of the medications as a fence that keeps the virus out. Miss one dosage, and suddenly there’s a hole in the fence that allows the virus to slip through.

Soon the virus mutates and takes over.

Once that happens, the drugs used to treat the disease-along with all the mediation in that class-stop working. But it’s not just the person with HIV, who has fewer choices when it comes to medications. Anyone that person infects will also be resistant to the drugs.

Changing minds, hearts

At the weekly Ladies gathering, Karen speaks up: “I want a relationship, but I am afraid to tell him I have HIV.”

Veronica says that her new husband didn’t care when she told him.

“It’s where your heart is,” she says. “We can’t make everyone love us.”

Another member pipes up that she found love after HIV and that her husband isn’t bothered by the diagnosis.

Karen insists: “If a person knows you and likes you, HIV shouldn’t change their mind.”