*This is an archive page. The links are no longer being updated. 1994.09.08 : Minority AIDS Congress Contact: Rayford Kytle or Pat Norris (202) 690-6867 Thursday, Sept. 8, 1994 HHS TO HOST MINORITY AIDS CONGRESS Building bridges and breaking down barriers will be the main agenda for a national congress on HIV/AIDS in racial and ethnic communities, hosted by the HHS Office of the Assistant Secretary for Health and the U.S. Public Health Service at the Sheraton Washington Hotel in Washington, D.C., Sept. 15-18. More than 700 community leaders, service providers and researchers from American Indian and Alaskan Native, Asian and Pacific Islander, Hispanic/Latino and African-American communities from across the United States will join with their federal and state counterparts to review HIV/AIDS policies and programs and identify future action steps to attack the AIDS epidemic in their respective communities. Speakers from the federal government include HHS Secretary Donna E. Shalala, interim national AIDS policy coordinator Patsy Fleming, Public Health Service director Philip R. Lee, M.D., and Surgeon General M. Joycelyn Elders, M.D. Secretary Shalala said, "Nineteen federal agencies and offices have contributed to making this congress an event which will strengthen their partnership with leaders of communities historically underserved and hard hit by the AIDS epidemic." PHS director Lee added, "The meeting provides a unique opportunity for members of minority communities to learn from each other and work with federal HIV/AIDS specialists to remove obstacles which prevent minority members from receiving the resources and information they need to fight this epidemic." Tom Valverde, president of the Hispanic AIDS Coalition of Greater Kansas City, and one of the congress' community co-chairs, said, "This congress shows a true partnership between community leaders and the government. We look forward to working together to develop more effective, culturally sensitive HIV/AIDS policy solutions." Other community co-chairs are Robyn Tirell of Life Foundation in Honolulu, Hawaii; Rene Whiterabbit of the Indian Health Board in Minneapolis, Minn.; and Cornelius Baker, director of public policy for the National Association of People with AIDS. - 2 - The goal of the congress is to identify barriers to effectively addressing HIV/AIDS issues in minority communities. These barriers may be cultural -- such as social mores which inhibit frank discussion of the issues; structural -- such as scarcity of minority organizations, adequate funding and representation on AIDS policy-making bodies; and psychological -- such as denial that HIV/AIDS is a problem in these communities. Participants will develop individual action plans which will help them build bridges between their communities and government and private resources. The congress will focus on three areas: Prevention: Issues regarding HIV prevention within racial/ethnic populations, including community planning, developing school-based programs and targeting incarcerated individuals, rural migrants, gay men and lesbians. Services: Issues related to service delivery, including those surrounding Ryan White Care legislation, housing, access by women and children, continuum of care, correctional facilities and cultural competence. Research: Issues regarding access to clinical trials, benefits and risks of AZT therapy to reduce maternal transmission of HIV, alternative/complementary therapies and data interpretation. Although HIV can infect anyone who engages in behavior which puts them at risk, the incidence of HIV/AIDS in some racial and ethnic communities is greater than in the general population. Four racial/ethnic minority groups -- African-Americans, Native Americans and Alaskan Natives, Hispanic/Latino and Asian and Pacific Islanders -- make up about 26 percent of the U.S. population, but about 50 percent of all reported AIDS cases in the United States. They account for 75 percent of reported cases in U.S. women and 80 percent of reported cases in U.S. children under the age of 13. AIDS is now the leading cause of death for African- Americans aged 25 to 44 and the second leading cause of death for Hispanic/Latino adults in that age group. A national conference in 1989 focused on HIV/AIDS in racial and ethnic communities. The new congress grew out of recommendations made by representatives from eight subsequent regional minority AIDS conferences held in 1991 by the PHS Office of Minority Health. Representatives of racial and ethnic groups were involved in planning the congress. Planning committee members were chosen not only for their expertise and experience in HIV/AIDS, but also to help ensure representation based on race/ethnicity, gender, sexual orientation, HIV status, rural/urban location and professional background. ###