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National Minority AIDS Council : ウィキペディア英語版
National Minority AIDS Council

The National Minority AIDS Council (NMAC), a nonprofit organization located on the U Street Corridor of Washington, D.C., was founded in 1987 to “build leadership within communities of color to address the challenges of HIV/AIDS.” The sole national organization addressing the AIDS epidemic in communities of color, NMAC represents over 3,000 community- and faith-based organizations nationwide. The agency advances its mission by providing minority and minority-serving faith- and community-based organizations a variety of capacity building assistance programs, online and classroom-based trainings, printed and electronic resources, grassroots organization and political advocacy. These activities help these agencies deliver HIV/AIDS services more efficiently and effectively, ultimately helping to mitigate the impact of HIV/AIDS in underserved and marginalized communities.〔National Minority AIDS Council: http://www.nmac.org/index/mission-statement〕
==History==

Since AIDS symptoms were first described in June 1981 in the ''Morbidity and Mortality Weekly Report'', AIDS has disproportionately affected minorities. A nurse named Joan Vileno, of Montifore, a health care facility in the Bronx, New York, recounted in Jane Gross' ''New York Times'' article, “The State of AIDS, 25 Years After the First, Quiet Mentions; The Nurse,” that the majority of her patients in the early 1980s were minority heterosexual IDUs (injecting drug users). Many delayed seeking medical care due to AIDS' close association with homosexuality. All of her patients died, many of them estranged from their families.
Leaders of prominent minority AIDS organization nationwide – including Paul Kawata, Gil Gerald, Calu Lester, Don Edwards, Timm Offutt, Norm Nickens, Craig Harris, Carl Bean, Suki Ports, Marie St.-Cyr and Sandra McDonald – started the National Minority AIDS Council (NMAC) in response to the American Public Health Association (APHA) decision to not invite anyone of color to participate on the panel of its first ever AIDS workshop, at its 1986 association meeting. Harris, an African-American gay man living with AIDS, announced the formation of NMAC during that panel discussion after he rushed the stage, shouting "I WILL BE HEARD" and took the microphone away from Dr. Merv Silverman, then the San Francisco Health Commissioner.
NMAC then set about building awareness of the impact of HIV in communities of color. It met with US Surgeon General C. Everett Koop while he was writing his historic report about AIDS. Originally scheduled for just 15 minutes, Koop, who had not known about the disproportionate impact of HIV/AIDS among minorities, sat riveted by NMAC's representatives for nearly two and half hours. The report would become the only publication, other than tax and census forms, to be mailed to every person in the United States.
The agency incorporated in 1987, and later launched the groundbreaking social marketing campaign, “Live Long Sugar,” with Patti LaBelle, which alerted people of color living with HIV/AIDS about the dangers of the common HIV co-infection, Pneumocystis carnii pneumonia (PNP).
In 1989, NMAC partnered with the Centers for Disease Control and Prevention (CDC) to help build the capacity of small faith- and community-based organizations (F/CBOs) delivering HIV/AIDS services in communities of color. This changed the mission of the agency from raising awareness of the impact of HIV/AIDS among minorities, to building leadership within communities to address the challenges of HIV/AIDS.
Three decades after Vileno’s writings, HIV still disproportionately impacts communities of color. African Americans and Latinos, who each represent 18% of the U.S. population, account for over 50% and 18% of all new HIV cases reported to the CDC each year, respectively. In 2008, according to the CDC, African-Americans accounted for 52% of all new HIV/AIDS infections.〔Centers for Disease Control: http://www.cdc.gov/hiv/surveillance/resources/reports/2008report/commentary.htm〕 And AIDS is the leading cause of death among African American women aged 24–35. But NMAC continues to struggle on minority communities’ behalf with a community-based response of public policy education programs, conferences, treatment and research programs initiatives, trainings, and electronic and printed resource materials.

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