Saving Face and Saving Lives in the Bay Area's Asian and Pacific Islander Community

Karin McKie READ TIME: 6 MIN.

For many Asian and Pacific Islanders (API) in the Bay Area, the fight against HIV/AIDS awareness and testing is complicated by stigma and the need to "save face," or protect families from perceived public disgrace. Groups like San Francisco's Asian & Pacific Islander Wellness Center and Silicon Valley's Asian Americans for Community Involvement help battle stigma and increase HIV testing among APIs.

"Saving face is not a negative cultural trait, but an embodiment of our respect for family and community," said APIWC's Community Development Director Lina Sheth. "We have to work within our culture to redefine the concept, to show that talking about sex and HIV is actually protecting the needs of the group. This shift requires courage, strength and compassion."

The API cultural concept of "saving face" contributes to lack of discussion and action in this community regarding drug use, sexuality and sexually transmitted infections like HIV. APIWC reports that 1 in 3 API people who are living with HIV don't know it, likely due to fear about personal information that testing might expose. Once HIV status is known, families might shun, isolate or discriminate against an HIV-positive relative.

"When I was diagnosed with HIV, my mother wanted me to come home so she could take care of me. At first, I was relieved, but I soon realized that 'taking care of me' really meant she wanted to keep me hidden. She wanted to sweep me and the shame of my HIV status under the rug," said Henry, an APIWC client.

This harmful side of "saving face" can increase HIV risk and manifestation, because shame could keep people from testing and treatment. Fear and secrecy can cause depression, which might lead to further unsafe behaviors. Plus, APIWC's Dr. Tri Do cautioned, "We know that psychological stress hastens HIV progression."

APIWC reports that nearly two-thirds of Asians, and more than 70 percent of Native Hawaiians and other Pacific Islanders, have never been tested for HIV. The Centers for Disease Control and Prevention (CDC) said that the number of APIs living with AIDS has risen about 10 percent.

"APIs are often tested very late in the development of their disease, most likely due to stigma," Sheth added, noting that healthcare providers and systems must begin to address this additional cultural component in diagnosis and treatment.

To this end, APIWC and the Asian and Pacific Islander American Health Forum (APIAHF), with offices in San Francisco and Washington, D.C., have contributed material to "BESAFE: A Cultural Competency Model for Asians and Pacific Islanders." Produced by the National Minority AIDS Education and Training Center at the Howard University College of Medicine in 2009, the online PDF document is an API cultural sensitivity resource for HIV/AIDS care providers.

"However, additional resources are needed," said APIAHF's V.P. of Community Strategies Ed Tepporn.

HIV rates in the API population have also been statistically ambiguous. The number of cases may be unreliable due to underreporting, and states like California, with large API populations, are not included in current CDC HIV/AIDS data sets, which lumps the group under "other."

"For 30 years, API advocates have been asking not to be classified as 'other,'" said Sheth. "So the CDC is now developing a multi-disease narrative for specific ethnic groups, which is exactly what communities need to build better prevention and public health responses."

The Banyan Tree Project is "Taking Root"

In addition to their Tenderloin neighborhood-based organization providing health services, education and research, APIWC, now in its 25th year, also created The Banyan Tree Project, "Rooted in Acceptance," as a national social marketing program to combat cultural shame.

Banyan Tree includes a digital storytelling initiative called "Taking Root: Our Stories, Our Community," which address stigmatized beliefs and attitudes that are meshed with prejudice and emotion.

"The shortest distance between two hearts is a story," said Sheth. "You can't listen to the hearts of these storytellers, these painful and honest personal narratives, and refuse to question your beliefs. The power of these individual stories is inspiring."

"Taking Root" is a long-term project that offers three-day intensive workshops to empower and teach storytellers how to create two- to four-minute personal narrative videos with voiceovers, video and audio clips. The produced work is unfiltered, and storytellers decide how much they want to share. Non-English speakers can share stories in their native tongues.

The group plans to have about 60 stories produced by the end of 2013, created out of their free workshops. In the Bay Area, trainings have been held at Berkeley's Center for Digital Storytelling. Additional storytelling workshops will be held on Guam from November 16-18, in Honolulu and Atlanta in spring 2013, and in New York City next summer. Together, these stories will create a meta-story of HIV in the API community, a truthful narrative to combat the monolithic notion of a "model minority."

"Smart Asian Woman" Stereotype Leads to Increase in HIV Infection

In addition to "face," another cultural stigma, although seemingly complimentary, curtails discussion and testing: the "smart Asian," and particularly the "smart Asian female," stereotype. This perception of APIs can prevent timely testing due to the assumption that well-educated people, especially women, have low HIV risk.

According to APIWC, sexually experienced API women are least likely to be offered an HIV test than women of other ethnicities during doctor visits. Data shows that 26 percent of African-American women were offered testing, 22 percent of Caucasians, 20 percent of Hispanics and only 17 percent of API women are asked. Plus, API women are four times more likely to get an STD than API men.

"I knew that I had been in a few risky sexual situations," Naina told APIWC, "so I wanted to get an HIV test. My doctor told me as an Asian woman, I wasn't really at risk. He said, 'Don't worry about it.' I tried to get tested three different times. Finally, I got a test in another country. I was HIV-positive."

APIWC reports that about 80 percent of HIV-positive API women are infected via heterosexual sex, and, according to CDC data from the Morbidity Mortality Weekly Report, that they had the largest rate of increase in new HIV infection in the nation, higher than any other racial or ethnic group.

South Bay A&PI HOPE

In Silicon Valley, Asian Americans for Community Involvement (AACI) addresses API wellness issues including healthcare for all, regardless of ability to pay, in languages such as Cantonese, Mandarin, Burmese and Vietnamese. AACI offers mental health services, the Center for Survivors of Torture, plus services in HIV Outreach, Prevention & Education (HOPE), including free OraQuick rapid testing, counseling, advocacy and discussion groups. AACI addresses HIV stigma with projects such as the Condom Kitchenette, which distributed 11,250 condoms in 2009.

To put focus on cultural exclusion and to encourage dialogue about the disease, APIWC and Banyan Tree started the National Asian and Pacific Islander HIV/AIDS Awareness Day in 2005, held annually on May 19. The 2011 theme was "Saving face can't make you safe. Talk about HIV -- For me, for you, for everyone."

For more info, visit aids.gov/news-and-events/awareness-days/asian-pacific-islander/.

For More Information

� Asian Americans for Community Involvement HIV testing, San Jos� 408-278-4138, [email protected], hiv.aaci.org
� Asian and Pacific Islander American Health Forum, San Francisco, 415-954-9988, www.apiahf.org
� Asian and Pacific Islander Wellness Center, San Francisco, 415-292-3400, www.apiwellness.org/home.html
� Banyan Tree Project, 866-5BANYAN, www.banyantreeproject.org
Twitter hashtag #withoutshame
� BESAFE publication at www.aids-ed.org/pdf/etres/API_BESAFE.pdf
� CDC Asian and Pacific Islander statistics -http://www.cdc.gov/Hiv/resources/factsheets/API.htm


by Karin McKie

Karin McKie is a writer, educator and activist at KarinMcKie.com

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