HIV infection affects millions of people around the world, including in the United States. According to the United Nations, there has been a 32 percent decrease in the annual rate of new HIV infections worldwide since 2010. Even though the number of new HIV infections has gone down, it's important to know that they’re still occurring. HIV is a lifelong condition, and it affects different groups of people in different ways. Two groups who are disproportionately affected by HIV are Black people and Latino people.
Understanding how race and identity are connected to HIV rates is crucial for stopping the spread of the virus and ensuring that everyone who is affected can get the right care. In this article, we’ll discuss HIV prevalence (how common HIV is), how HIV affects different communities, and the barriers that prevent people from getting the care they need.
In 2019, around 1.2 million people aged 13 and older in the U.S. were estimated to be living with HIV infection. However, HIV infection does not affect all groups of people equally. A few of the groups that are more impacted by HIV include Black and Latino people, those who identify as transgender, people who inject drugs, and men who have sex with men.
Black and Latino communities in the U.S. have higher rates of HIV infection compared to other groups. More people from these communities get infected with HIV and experience HIV-related health problems than those in other communities.
From 2017 to 2021, the Centers for Disease Control and Prevention (CDC) reported the rate of HIV diagnosis in Black/African American people decreased by 10 percent, while the rate of HIV diagnosis among Hispanic/Latino people remained stable. Despite this finding, Black/African American and Hispanic/Latino people together still made up the majority of new HIV diagnoses in 2021.
There are several reasons why HIV infection rates are higher in Black and Latino communities. Some factors include economic challenges, like poverty and limited access to health care, as well as cultural and social factors that affect how people seek help and learn about HIV prevention. Bigger issues like homophobia, racism, and discrimination make the impact of HIV worse in these communities. They can also make it harder for people to access health care, education, and stable jobs, which are all important for preventing and treating HIV.
Another group that is disproportionately affected by HIV are people who identify as transgender or as a gender other than male or female. Transgender individuals are those whose gender identity is different from the gender they were assigned at birth. From 2017 to 2021, the CDC reported an increase in the number of transgender people who were diagnosed with HIV. The prevalence of HIV infection tends to be higher for transgender women than for transgender men. On the other hand, the number of cisgender people (those whose gender matches the one they were assigned at birth) diagnosed with HIV has decreased.
Transgender people face unique challenges when it comes to preventing HIV and getting proper care. Factors like stigma, discrimination, difficulties in accessing health care, and a lack of gender-affirming medical support can make people who identify as transgender more vulnerable to HIV.
People who use needles to inject drugs have a higher risk of getting HIV. The CDC reported that in 2021 in the U.S., more than 2,500 people were diagnosed with HIV due to injected drug use. While white people made up the largest portion (49 percent) of new HIV diagnoses associated with injected drug use in 2021, Black/African American and Hispanic/Latino people made up the majority of all people living with HIV due to injection drug use (44 percent and 27 percent, respectively).
Gay men, bisexual men, and other men who have sex with men are also more likely to be affected by HIV. In 2021, 67 percent of new HIV diagnoses were among men who reported having sexual contact with other men. There are more than 620,000 men who have sex with other men and live with HIV in the U.S., and this group makes up almost half of the total number of people living with HIV in the U.S.
You’ve probably noticed that a lot of the people diagnosed with HIV belong to more than one of these groups. This overlap in identity is called intersectionality. People who belong to multiple marginalized communities may face discrimination or social disadvantages for various reasons and may have a higher risk of contracting HIV compared to those who don't have these overlapping identities. For example, Black gay and bisexual men face a higher risk of getting HIV. Similarly, transgender individuals within Black and Latinx communities may face unique challenges that increase their vulnerability to HIV.
Several factors can help limit the spread of HIV and reduce its impact on people and communities.
In 2019, the CDC estimated that about 13 percent of the total number of people with HIV in the U.S. did not know their HIV status. The CDC recommends that everyone between the ages of 13 and 64 be tested for HIV at least once, and more often if they fall into a higher-risk group. Testing allows you to know your HIV status, so you can receive the treatment and care you need if you test positive. Additionally, knowing your HIV status is important so you can prevent the spread of the virus to other people.
Several things can reduce the risk of getting or spreading HIV. These strategies include:
HIV viral suppression refers to decreasing the viral load (the amount of HIV in the body) to undetectable levels using antiretroviral therapy (ART). This helps to maintain the health of the person living with HIV and prevent HIV from spreading. In fact, the CDC reports that there is no risk of spreading HIV to sexual partners if a person’s HIV viral load is undetectable for at least six months straight and they are taking ART.
For some people, getting the necessary care and support for HIV can be difficult, especially if they come from marginalized groups. It’s important to understand the barriers that prevent people from accessing the care they deserve. A few of the common obstacles include less access to health care, a lack of HIV awareness, and social stigma.
It’s not always easy to find health care services for HIV. Here are a few reasons why:
Not having enough knowledge about HIV can create barriers to care. Some important factors include:
Several social factors can make it challenging to access HIV care. These include stigma, lack of support from loved ones and the community, and discrimination based on factors like race, gender, or sexual orientation.
By acknowledging the differences in how HIV affects groups of people and taking action, we can work toward achieving fairness and better health for everyone affected by HIV.
Everyone, especially those who may be at higher risk for HIV, should prioritize their health by getting tested. Remember, receiving a proper diagnosis is an important first step toward accessing the care and support you need. Don’t hesitate to reach out for help, especially if you belong to a community that may have a greater risk for HIV.
By working together and educating ourselves, we can create a future where everyone, regardless of their race or background, has equal opportunities for HIV prevention, testing, and care.
On myHIVteam, the social network for people with HIV and their loved ones, more than 41,000 members come together to ask questions, give advice, and share their stories with others who understand life with HIV.
Have you been diagnosed with HIV? Did you know that some people of different races and backgrounds have a higher risk for HIV? Share your experience in the comments below, or start a conversation by posting on your Activities page.
Get updates directly to your inbox.
Become a member to get even more:
A myHIVteam Subscriber
It seems perfect to me that they help the population with their talks about HIV
Me parece perfecto que ayuden a la población con sus charlas sobre VIH
We'd love to hear from you! Please share your name and email to post and read comments.
You'll also get the latest articles directly to your inbox.