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Category: HIV / AIDS

New Guidelines: Make HIV Testing Routine

new HIV screening guidelinesThe U.S. Preventive Services Task Force (USPSTF) recently released new recommended screening guidelines for HIV. It gave a grade A recommendation for routine HIV screening for everybody aged 15 to 65, and younger adolescents and older adults at an increased risk for HIV infection. It also gave a grade A recommendation for HIV screening for all pregnant women, including those in labor whose HIV status is not known.

 

What Is a Grade A Recommendation?

Many health organizations, professional societies and medical quality review groups use USPSTF’s recommendations to make decisions about their clinical standards. And under the Affordable Care Act (ACA), private health insurance policies created after March 23, 2010, are required to offer all preventive services that have been given an A or B recommendation by USPSTF, at no out-of-pocket cost to the consumer. ACA also gives state Medicaid programs financial incentives to cover USPSTF-recommended preventive services for adults.

The Centers for Disease Control and Prevention (CDC) says roughly 1.1 million Americans are living with HIV. Because HIV infection does not usually cause symptoms in its early stage, many people (about one in five) who are HIV positive are unaware they are infected, making them more likely to transmit the virus their sexual partners. According to the CDC, nearly 50 percent of all new HIV infections are transmitted by people unaware they are infected. This is especially critical in the black community, where African-Americans accounted for an estimated 44 percent of all new HIV infections among adults and adolescents (aged 13 years and older) in 2010, despite representing only 12 percent to 14 percent of the United States population, and where nearly 100,000 were unaware of their HIV status in 2009.

 

The Benefits of Knowing Your Status

Once identified by screening, the hope is that HIV-infected folks can begin antiretroviral therapy, adhere to treatment and achieve full viral load suppression (no detectable virus in the blood). A suppressed viral load means better health outcomes for infected people, as well as less chance of infecting partners.

Under the new guidelines, HIV screening will be easier for medical staff since they will no longer need to find out a patient’s risk status before offering testing.

Routine testing will also help reduce the proportion of late HIV diagnoses. One-third of people with HIV are diagnosed so long after they acquire their infection that they develop AIDS—the final stage of HIV disease—within one year of diagnosis. They could have been HIV positive for as long as 10 years before being diagnosed and unable to take advantage of HIV treatment.

 

Related Posts

Alicia Keys Shines Light on Women and HIV

Older Adults and HIV Testing

New HIV Infection Rate Drops Among African-American Women

Many HIV-Positive Youth Don’t Know Their Status

Alicia Keys Shines Light on Women and HIV

alicia keys empowered campaignOne in 32 African American women in the United States is likely to be diagnosed with HIV in her lifetime.

“One in 32, think about that,” said singer-songwriter Alicia Keys, citing the Centers for Disease Control and Prevention statistic at an event Monday. “Thirty years after we first heard of AIDS, it is really a tragedy that anybody is being infected.”

But people are being infected with the virus in the U.S. and, as Keys said, black women are affected disproportionately. Keys stammered a little as she read the word “disproportionately” from her notes, and then recovered and repeated it with force saying, “It’s a big word and it’s a bad thing. That’s not acceptable.”

Keys’ comments came at the kickoff of the EMPOWERED campaign, an effort to increase awareness of HIV and AIDS among women, a new part of the Greater Than AIDS public information push by the Kaiser Family Foundation. (Kaiser Health News is an editorially independent part of the foundation.)

The CDC statistics on women in general and black women in particular are sobering.

  • There are more than 1.1 million people living with HIV in the U.S., and one-in-four of them are women.
  • The rate of infection for black women was 20 times higher in 2010 than it was for white women (38.1 per 100,000, compared to 1.9 per 100,000).
  • In 2010, 60 percent of women with HIV were African American, 19 percent were Latino, and 18 percent were white, according to the CDC.
  • Newly infected black and Latina women are more likely to be younger, with 23 percent of black women and 21 percent of Latina women in the 13-24 year old age range.
  • In 2009, black women accounted for the greatest share of deaths among women with HIV at 65 percent, followed by white women at 17 percent and Latinas at 14 percent.

One of the main themes of the campaign–which includes videos, public service ads, and social media efforts—is to make the issue personal for women. A video shows Keys interviewing five women living with HIV. “They are just like you and just like me,” Keys says in the video of the women, who all sat in the front row of the foundation’s conference center during Monday’s kickoff.

Valerie Jarrett, senior advisor to President Barack Obama, and chairwoman of the White House Council on Women & Girls, also spoke at the event, making the point that the issue of women and AIDS has long been a personal one for her.

“Every day I carry around the heartbreak of losing my sister-in-law, who died nearly 20 years ago,” Jarrett said. “She went months without being diagnosed because nobody thought to test a married woman at the time.”

Jarrett pointed out that, under the Affordable Care Act, HIV testing is now covered as a preventive service without cost sharing, and beginning in 2014, people with HIV cannot be denied insurance because of a pre-existing condition.

—Diane Webber

This story originally appeared on Kaiser Health News. Kaiser Health News is an editorially independent program of the Henry J. Kaiser Family Foundation, a nonprofit, nonpartisan health policy research and communication organization not affiliated with Kaiser Permanente.

Older Adults and HIV Testing

aids awarenessToday’s sobering statistic: One out of every four people living with HIV/AIDS is 50 or older. What’s worse is that many of them are unaware they have HIV because they haven’t been tested, putting themselves and others at greater risk.

Not knowing their status puts these older adults at increased risk of late diagnosis. According to the Centers for Disease Control and Prevention, 43 percent of HIV-positive people between the ages of 50 and 55, and 51 percent of those 65 or older, develop full-blown AIDS within a year of their diagnosis. They account for 35 percent of all AIDS-related deaths.

 

What’s Standing in the Way of HIV Testing

Though several barriers may prevent this population from getting tested, a new study out of UCLA found the chief reasons are a mistrust of the government and conspiracy theories about AIDS.

“Our work suggests that general mistrust of the government may adversely impact peoples’ willingness to get tested for HIV/AIDS,” said Chandra Ford, an assistant professor of community health sciences at the UCLA Fielding School of Public Health and the study’s primary investigator, in a statement. “HIV/AIDS is increasing among people 50 and older, but there’s not a lot of attention being paid to the HIV-prevention needs of these folks. Older adults are more likely to be diagnosed only after they’ve been sick, and as a result, they have worse prognoses than younger HIV-positive people do.”

 

Analyzing the Barriers to HIV Testing

The study, which looked at a small group of people recruited from public health venues, found that 72 percent of the participants did not trust government, and they believe the government is run by a few big interests looking out for themselves. Another 30 percent believe in AIDS-related conspiracy theories, including that the virus is man-made and was created to kill certain groups of people. Forty-five percent of the study’s participants had not had an HIV test in the previous 12 months.

“The CDC recommends that anyone who’s in a high-risk category should be tested every single year,” Ford said in her statement. “These findings mean that the CDC recommendations are not being followed.”

 

Next Steps for Older Adults and HIV Testing

Researchers say they need to examine other groups of older adults to determine if these views are more widely held than just among the at-risk population in this study.

New HIV Infection Rate Drops Among African-American Women

For the first time, the rate of new HIV infections among African-American women declined 21 percent between 2008 and 2010, according to a Centers for Disease Control and Prevention (CDC) report released Wednesday. “We are encouraged to see some declines among African-American women,” says Joseph Prejean, chief of the Behavioral and Clinical Surveillance Branch in the CDC’s division of HIV/AIDS Prevention. “They’ve been one of the most severely affected populations. We’re cautiously optimistic that this could be part of a longer-term trend.”

Other experts are similarly hopeful. “There is much to be encouraged about in these new findings, particularly in terms of overall stability of new HIV infections and a decrease in HIV infections among African-American women,” says Jeffrey Parsons, Ph.D., professor in the psychology department at Hunter College in New York City and director of the college’s Center for HIV/AIDS Educational Studies and Training. This drop in new infections, he says, “is likely due to very targeted behavioral intervention programs for African-American women.”

While this good news is a step in the right direction, black women still account for nearly two-thirds of new infections among American women, according to the CDC report.

Other minorities also are disproportionately affected. Blacks represent just 14 percent of the population, yet they account for 44 percent of new HIV infections. Hispanics are 16 percent of the population, but account for 21 percent of new infections.

The overall number of new infections among Americans has remained stable at about 50,000 per year over the last decade. The CDC says this indicates that prevention programs, testing and treatment are having an impact, but rates of new HIV infections are still too high.

Related Articles:

Many HIV-Positive Youth Don’t Know Their Status

Born Positive: ‘AIDS Babies’ Grow Up

Many HIV-Positive Youth Don’t Know Their Status

The numbers are disturbing: A new Centers for Disease Control and Prevention (CDC) Vital Signs report found young Americans ages 13 to 24 make up more than a quarter (that’s 1 in 4 for those doing the math) of new HIV infections each year. Every month, 1,000 youth are becoming infected with HIV, the virus that causes AIDS. A whopping 60 percent don’t know they are infected. The majority, 83 percent, of these new infections is among males, with African Americans and gay and bisexual men being hardest hit. The cost of care for the young and newly infected is approximately $400,000 over a lifetime.

“Despite the great treatment we have, HIV remains an incurable infection,” says Thomas R. Frieden, M.D., director of the CDC. “Given everything we know about HIV and everything we know about how to prevent it, it’s unacceptable that young people are getting infected from an entirely preventable disease.”

What’s leading to this epidemic within the epidemic? A toxic brew of stigma, homophobia, lack of access to health care, risky behaviors and too few young people being tested for HIV—and therefore not knowing their status, the experts say.

“Young men who have sex with men were more likely to have four or more sexual partners,” explains Kevin Fenton, M.D., director, National Center for HIV/AIDS, Viral Hepatitis, STD and Tuberculosis Prevention. “High rates of HIV and other sexually transmitted diseases in many African-American and gay communities increase the risk of being infected with every sexual encounter. HIV-infected people younger than 25 are significantly less likely to get and stay in care.”

Seventy-five percent of young people in the study say they weren’t taught about HIV or AIDS in school.

“If we’re going to see a generation free from AIDS, we’re going to have to intensify education,” Dr. Frieden says. That means “expanding access to testing, both in the health-care setting and in the community. It requires all of us to do our part. Young people need to get educated and get tested. Parents need to talk to their kids early and often about sexual health and staying safe. Health-care providers should test people 13 and older and provide tailored prevention.”

And, he says, all Americans need to talk about this issue.

The CDC’s plan to combat this news is multi-pronged:

  1. Improving the treatment cascade is critical. This would lead to fewer people out there who have uncontrolled infection and more HIV-positive people in care with their viral load suppressed.
  2. Educate the at-risk population to reduce risky behaviors, including multiple partners, illicit drug use, alcohol abuse and eschewing condoms.
  3. Making sure everyone knows his or her status. This means getting tested for HIV is key. Currently, just 13 percent of high school students have been tested. For 18- to 24-year-olds, the testing statistic increases, but only to 35 percent.

“We have to focus on where the epidemic is and hit harder there. If we can knock risky behavior down by even 10 or 20 percent,” Dr. Frieden says, we’ll be on our way to an AIDS-free generation.

Born Positive: ‘AIDS Babies’ Grow Up

Hydeia Broadbent doesn’t remember a time when HIV wasn’t part of her life. Since age 6 the global AIDS activist balanced national speaking engagements and television appearances with bouts of sickness and doctor’s appointments.

Shantrell Jackson, who was born with HIV, remembers taking medication regularly as early as the first grade. Her pills were put into applesauce to make ingestion tolerable.

Lolisa Gibson’s mother transmitted HIV to her at birth. But decades later Gibson broke the cycle and delivered a healthy baby boy who doesn’t have the virus.

These women, all born with the virus that causes AIDS, were the babies born in the 1980s who were doomed to perish. But they beat the odds. They defied death predictions. They survived and now they thrive.

Broadbent, Jackson and Gibson inherited HIV, but they all made a choice to work to battle the disease and the stigma around it.

Thirty years into the AIDS epidemic medical advancements have prolonged the lives of babies born with HIV and reduced the rate of mother-to-child transmission. The fact that these women and girls are here is amazing, says Kimberly Bates, M.D., medical director of the Nationwide Children’s Hospital Family AIDS Clinic and Educational Services in Columbus, Ohio. “This is the cure for polio in my time,” Dr. Bates says. “Something that killed so many children 30 years ago is preventable. We can prevent mom from transmitting HIV to her child. Thirty years ago that was a dream.”

Since the early 1990s mother-to-child HIV transmission has declined by 90 percent, according to data from the Centers for Disease Control and Prevention (CDC). In 1991 there were about 1,700 cases annually of perinatal transmissions in the United States. Now that number is around 300. A woman with HIV has a 25 percent chance of transmitting the virus to her child. But with proper antiretroviral therapy treatment available now, that drops to 1 to 2 percent chance, the CDC says.

Progress in perinatal transmission and HIV care has meant saving lives, Broadbent says. “It was my childhood growing up in the hospital,” says Broadbent, 28. “It was normal for me always being sick, seeing my friends pass away.”

Life-prolonging medication also helps women born with HIV have quality of life and do the same thing their peers do, such as pursue careers, further their education and start families, Dr. Bates says. “They’ve had to do that all in the face of doing something that probably the majority of Americans couldn’t do, be almost perfect in taking care of their health,” she says. “Most Americans can’t remember to take a multivitamin every day.”

But living an entire life with HIV can sometimes overwhelm young women, says Dazon Dixon Diallo, founder of SisterLove, a women’s AIDS and reproductive health advocacy organization in Atlanta. “Adults infected later in life have memories of a life without AIDS,” Diallo says. “These women don’t.”

And the transition from childhood to womanhood can sometimes mean a transition out of consistent medical care. “They come through a system that nurtures kids,” she says. “Transitioning from that full care to self-care is a big transition, and we lose a lot of young people to that. They fall out of care. That could lead to losing their lives. If they’ve lost care it’s an opportunity for them to get sicker faster because they’re not in treatment.”

Shantrell Jackson, 27, of Dunwoody, Georgia, was always sick throughout childhood. But she says she didn’t learn she had HIV until she was 18. Jackson says she didn’t seek medical care for about a year to avoid the routine associated with the disease. “I kept saying I have an STD, but I’ve never had sex,” says Jackson, a former HIV camp counselor. “When I’m depressed I don’t want to take my meds. The meds are a constant reminder that you’re living with something you can’t control.”

Now she has more control over her emotions. Jackson, who has been working at SisterLove for three years, said she’s seen a therapist. And she keeps herself from slipping back into depression by going to church, meditating and attending support groups.

Broadbent says HIV may manifest itself physically, but the virus also has an impact on the mental health of those who’ve lived with it all of their lives, especially when they start dating.“It affects your mind, body and soul. If you are not secure with who you are it can be very depressing,” says Broadbent, who lives in Las Vegas. “You can think you can’t find love…. You wonder why me.”

Women born with HIV experience mental anguish because there is still stigma associated with the disease. The stigma surrounding sexual transmission of HIV is especially strong, Jackson says, but when people learn she came into the world with the virus, “they go from looking down on you to empathizing,” she says.

Jackson has developed and facilitated workshops for people her age to help them work through issues dealing with dating and disclosure.

Lolisa Gibson, 26, spent years working as an AIDS activist and educator disclosing her status to people across the country. But when she discovered she was pregnant she became concerned about disclosure. “I looked at my fiancé and I said how do I tell my baby I have HIV,” she says. “He said, ‘You tell him just like you tell everyone else.’”

Gibson’s son is now a healthy 3-year-old. She took antiretroviral drugs throughout her pregnancy to prevent transmitting the virus to her son. He also took medication soon after birth and was tested monthly.

Gibson says she learned she had HIV at age 16 after she became ill and her weight dropped to 95 pounds. She learned she had esophagitis and later tested positive for HIV. Tests indicated she had the virus for at least 10 years.

Resentment toward their mothers for transmitting the HIV virus to them still looms for some women who live with it. But Gibson says she focuses on maintaining a loving relationship with her mother now and not on actions of the past. “I can’t image the pressure of knowing you gave your child something they can’t get rid of,” says Gibson who lives in Brooklyn, New York. “My mom has shown me nothing but love and support.”

Gibson says her diagnosis led her to commit her life to working as an HIV advocate and educator. “When I learned I was positive, I didn’t have anyone to talk to,” she says. “They (counselors) were older white people who didn’t know what I was going through. I felt empty. I didn’t want another person to go through that.”

Broadbent also sees her diagnosis as a call to action. “I think this happened to me for a reason,” she says. “All of my struggles and everything I go through. I feel like I should be here telling my story and making people care about their life and their actions.”

—Sherri Williams

Stopping the Spread of HIV/AIDS

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HIV/AIDS

The Basics

HIV is short for “human immunodeficiency virus.”

  • How Do You Get HIV?

    You can get HIV through unprotected sex or by sharing needles or other equipment used to inject drugs.

  • Who Gets HIV?

    Anybody can get HIV. HIV is a virus; once it gets into your body, it can make you sick. It does so if you are rich or poor; 14 years old or 70; black or white; gay or straight; married or single. It’s what you do, not who you are, that puts you at risk for HIV.

  • How Long Does It Take to Feel a Symptom of HIV?

    People can have HIV for 10 years or more and never show any symptoms. Other people can get symptoms within a short time after being infected. The only way you can tell if you have HIV is to get an HIV test.

  • How Long Will I Live With HIV?

    If you keep your CD4 count up, keep your viral load down, take your HIV meds properly and live a healthy life, there’s no reason to think that your life will be any shorter with HIV than it would have been without it. The latest information on life expectancy for HIVers shows that HIV-positive people who are on treatment can expect to live well into their 60s and beyond — and the estimates keep getting closer to those of HIV-negative people as HIV meds become more and more effective.

  • What Should a Person Do After They Test Positive?

    If you’ve already tested positive for HIV, then there are tests a doctor can do to see whether your HIV is progressing, and whether it’s wise to start taking HIV medications.

    For most people, if HIV treatment is not started when their doctor recommends it (i.e., when their CD4 count is low or their viral load is high), eventually their immune system will weaken to the point that they may develop life-threatening health problems.

    If you’re newly diagnosed, it can also be incredibly beneficial if you seek out support, get help from your local HIV organization and connect with other HIV-positive people. Visit our “Just Diagnosed” page to read much more.

  • Where Did HIV Come From?

    The origins of HIV are still a little murky. Experts currently think that, about 100 years ago in Africa, an ancestor of HIV evolved into a form that jumped from monkeys to humans. The history of the global HIV pandemic is more recent, however: The world only began to pay attention to HIV in the early 1980s, when gay men in New York City and San Francisco began to die of a mysterious illness. The term “AIDS” — which is what doctors call it when HIV disease becomes advanced — wasn’t coined until 1982, and the virus now known as HIV wasn’t identified as the cause of AIDS until 1984.

HIV Testing 101

There’s only one way to find out for sure whether you have HIV: Get tested. Although some people feel symptoms when they’ve been newly infected with HIV, most people don’t. That’s one reason why HIV continues to spread throughout the world: Millions of people are estimated to be living with HIV without even knowing it. That’s why it’s so important for everybody to get tested regularly for HIV, if they have sex or use injection drugs.

It’s completely normal to get nervous, scared or even a little paranoid when you think you’ve put yourself at risk for HIV. An HIV testtaken at least six weeks after the risky event — can answer that question. Approved HIV tests are extremely reliable. There’s even a saliva test you can take at many doctor’s offices or clinics that will give you results in less than half an hour. (If it comes out positive, you’ll need to get an even more reliable blood test, known as a Western Blot, that will confirm the results in a couple of weeks.) And don’t forget, if you are at risk for HIV from sex, then you are also at risk for other sexually transmitted diseases that can be much easier to get.

If you live in the United States and are concerned about your privacy, in much of the United States, especially in cities, there are clinics and hospitals where you can be tested for HIV completely anonymously. There are even places that will help you notify past partners if you do test positive for HIV.

If you’d like to get tested for HIV, talk to your doctor or call a local HIV/AIDS hotline or HIV organizationto find out about trustworthy places you can go for testing.

If you live in the United States, you can get tested at no charge for HIV and other sexually transmitted diseases at state health departments. Planned parenthood also offers free testing. Check out this resource for a comprehensive list of HIV testing sites. Finally, don’t forget that if you test positive for HIV, it’s not the end of the world. Even if you don’t have health insurance, you can get free HIV treatment and if you take care of yourself, you can live a long and healthy life.

HIV/AIDS in Black America

n the fall of 1991, during a game of capture the flag in my eighth grade gym class, the teacher told us to stop playing, get in two lines and be very quiet. She told us that a serious announcement was going to be made. A few minutes later, over the speaker system, the principal played a press conference that was on the news. Earvin “Magic” Johnson, star of the Los Angeles Lakers basketball team, announced to the world that he was HIV positive.

I was completely shocked. Growing up, all I “knew” about HIV was that it was a white disease, and a gay one–except for Ryan White, who somehow contracted HIV through a blood transfusion. I was under the impression that this was not something that black people had to worry about.

Twenty years have passed since Johnson’s public disclosure, and so much has changed.

The face of this epidemic in the U.S. is now one that resembles mine. AIDS is the number one killer of black women ages 24-35. Black men who have sex with men (MSM) have the highest HIV rate among all racial groups of MSM. Overall, while African Americans make up a mere 14 percent of the overall U.S. population, they account for more than half of all new HIV infections that are diagnosed each year. And to make matters worse, African Americans are more likely to be diagnosed with HIV and AIDS at the same time than any other racial group, meaning they’re less likely to get tested until they’re very ill.

Black AIDS Institute’s chief executive and president, Phill Wilson, wasn’t exaggerating when he said that “AIDS is the fire that is ravaging the black community.”

So what exactly is fueling the flames?

There is no one answer. It’s a combination of many factors: Poverty and economic instability. Institutionalized racism. Lack of quality health care, poor access to health care in general and mistrust in the medical system. Gender inequality and domestic violence. Homophobia. Intravenous drug use and the lack of needle-exchange programs. Poor health literacy. High rates of incarceration. Untreated sexually transmitted diseases, such as herpes and gonorrhea, which make people more vulnerable to contracting HIV. And people having unprotected sex while unaware that they are positive, and who thus go untreated while they’re highly infectious.

The slow response by the federal government has played a role as well, as has a lack of funding. Thirty years into the epidemic, and it was only just last year that the U.S. government finally released a national HIV/AIDS strategy.

But most importantly, the black community’s own slow response to the epidemic has had a profound impact. Minus a few exceptions, most black media publications, churches and community leaders set the tone early by turning a blind eye to HIV, believing that this epidemic was not their problem and that HIV was a moral issue as opposed to a public health crisis. In the end, we have all paid a price for their unwillingness to address the disease early on.

Don’t get me wrong: Over the years, we have seen some progress in having public conversations about HIV, and the importance of getting tested and practicing safer sex. But we still have a long way to go. Unfortunately, too many current conversations about HIV — especially in the black media — are either met with resistance, treaded lightly or saturated with inaccuracies (think: everything about the down low).

Even within the past year, I have heard stories from people living with HIV who have recently been forced to eat off paper plates because those around them are still unaware of how HIV is contracted. Or how they are turned away from their church or rejected by loved ones and friends. I still come across people who don’t really know what HIV is, who believe wholeheartedly that AIDS is a government conspiracy to kill black folks, or who believe that they are not at risk for HIV because their sexual partner is not a gay man. The culture of ignorance, stigma, silence and fear is very real, and it is killing us.

Now is the time for change — and that change begins with you. This is why our African-American HIV/AIDS Resource Center exists.

By providing a diverse range of articles, first-person interviews and resources about HIV in black America, our goal is to give you hope and help bridge the knowledge gap between what you don’t know and what you need to know. Most importantly, this resource center is for everyone, not just those who are living with HIV. So, if you are a loved one or a caretaker of someone living with HIV, or you’re simply interested in learning more about HIV, AIDS and safer sex, this is a place for you too.

  • Our HIV & Me: An African American’s Guide to Living With HIV can help answer questions about when to start treatment, getting linked to care, finding support and how and when to disclose one’s status to others.
  • Our HIV/AIDS Info & Resources for African Americans section offers up info on current statistics, HIV prevention news, African-American HIV/AIDS organizations and hot-button issues such as HIV and the black church.
  • Our Personal Profiles section puts a face to the epidemic, helps reduce stigma and reminds people that they are not alone by boasting dozens of interviews with African Americans who are living and surviving with HIV.
  • Our Movers & Shakers section highlights talented and dedicated individuals who are part of the driving force behind efforts to end the HIV epidemic in African-American communities.
  • We have a great selection of African-American bloggers and columnists–some straight, some gay, some positive and some negative — who discuss their take on current events, personal experiences and HIV policy.
  • And for our Word on the Street page, HIV activists and health professionals share their thoughts on the most pressing issues impacting the black HIV epidemic.

We hope that our African-American HIV/AIDS Resource Center inspires you to join the fight and keep the faith. Because even though it is a steep, uphill battle, remember that it is winnable. It won’t be easy, but if everyone in our community can step up, get educated about the disease, get tested and take control and responsibility for our health, anything is possible.

From The Body