Janice E. Nichols
University of South Florida
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Anthropology & Medicine | 1999
Roberta D. Baer; Susan C. Weller; Lee M. Pachter; Robert T. Trotter; Javier E. García de Alba García; Mark Glazer; Robert E. Klein; Tracey Lockaby; Janice E. Nichols; Roger Parrish; Bruce Randall; Jeanette Reid; Susan W. Morfit; Van Morfit
Abstract This paper focuses on variability in beliefs about AIDS among Latin Americans, as compared with middle class Americans. Four geographically dispersed groups of Latin Americans were chosen for study as well as a middle class, largely Anglo‐American population. Coherent sets of beliefs were found at each site, and despite tremendous variability among the five populations, beliefs were remarkably similar across sites. The biomedical model is widely shared, and the critical variable in the extent to which it is understood is community prevalence of AIDS.
Aids Patient Care and Stds | 1999
David C. Speer; Margaret Kennedy; Mary R. Watson; Joan M. Meah; Janice E. Nichols; Betty J. Watson
Although the prevalence of AIDS among middle and older adults is increasing, little is known about them. The objective of this study was to obtain basic demographic and social information about people with HIV/AIDS (PWAs) over the age of 44 years. This was a descriptive, cross-sectional survey of convenience samples of 76 African-American (AA) and 80 White older PWAs. Participants were interviewed by trained peer interviewers using a structured and largely objective schedule. Participants and interviewers were each paid
Aging with HIV#R##N#Psychological, Social, and Health Issues | 2002
Janice E. Nichols; David C. Speer; Betty J. Watson; Mary R. Watson; Tiffany L. Vergon; Colette M. Vallee; Joan M. Meah
35 per completed interview. The schedule consisted of wide-ranging demographic, HIV/AIDS, stressor, coping, social, and support questions. Although both ethnic groups had incomes significantly below national norms and poverty rates three times their national rates, AA PWAs were markedly disadvanted socioeconomically relative to White PWAs. Although over 60% of all PWAs reported that having enough money to live on was a problem, AAs also reported significantly more Stressors, many related to economics, then White PWAs. AA PWAs reported being predominantly heterosexual, while the largest group of Whites was homosexual or bisexual. Sources of infection paralleled sexual orientation. Both groups used relatively effective coping strategies and reported moderate levels of social support and activity. It was concluded that the course of illness, treatment, and quality of life of middle and older PWAs are likely to be complicated by economic factors, and this will be particularly serious among AA PWAs.
Aging with HIV#R##N#Psychological, Social, and Health Issues | 2002
Janice E. Nichols; David C. Speer; Betty J. Watson; Mary R. Watson; Tiffany L. Vergon; Colette M. Vallee; Joan M. Meah
Publisher Summary This chapter discusses the distinction between mental-health problems that existed prior to human immunodeficiency virus (HIV) infection and those with post-HIV onset. Pre-existing problems are conceptualized as producing or contributing to risk behavior and thus to HIV infection; postinfection mental-health problems may also interfere with treatment for HIV and contribute to infection of others. The mental health and HIV/AIDS literature, some studies of older adults, the West-central Florida Older Adult project findings, treatment issues, and suicide factors are reviewed. Considering the tremendous number of stressors that people living with HIV (PLWHIV) must deal with and the high prevalence of mood disorders, suicide is a reasonable concern with this population. Psychiatric morbidity, alcohol and drug abuse, and behavioral disorder have also been viewed as risk factors for suicide. There is no disagreement that mental-health problems, disorders, and psychological distress are highly prevalent among both PLWHIV and people at risk for HIV infection. Even though suicide rates among PLWHIV are not clear, this issue is a serious concern for a variety of reasons. The chapter lists recommendations and encourages increased investment of resources in the prevention programs.
Archive | 2002
Janice E. Nichols; David C. Speer; Betty J. Watson; Mary R. Watson; Tiffany L. Vergon; Colette M. Vallee; Joan M. Meah
This chapter depicts graphically the diversity of older people impacted by human immunodeficiency virus (HIV) disease and the varied responses that they may have to their diagnosis. It is based on extensive and relatively unstructured narrative interviews with 15 older people living with HIV (PLWHIV), and provides a personal glimpse of the impact the HIV diagnosis has on their lives. The chapter opens with a biographical overview of the participants, followed by excerpts from their interviews, reflecting the range of their experiences pertaining to frequently mentioned aspects of living with HIV. The participants described the circumstances leading them to testing and their initial responses to the HIV diagnosis. Although at the time of their diagnosis, most of the participants had little understanding of HIV disease and what it might mean for them, they shared a sense that they had somehow become tainted or diminished because of it. The narrative research participants experienced a high degree of anxiety at the time of their HIV diagnosis. A number of specific issues were mentioned by the participants as being particularly stressful as they confront life as an older adult with HIV disease.
Archive | 2002
Janice E. Nichols; David C. Speer; Betty J. Watson; Mary R. Watson; Tiffany L. Vergon; Colette M. Vallee; Joan M. Meah
The chapter presents a case study of an individual infected by human immunodeficiency virus (HIV).. It illustrates a number of issues that have been raised while working with older people living with HIV disease (PLWHIV). It states that postdiagnosis, many older people are too often found forced to live their lives in a manner that differs greatly from the way they had planned—their reality often falls far short of the dreams toward which they worked throughout their careers. People who are considered to be middle-aged are often at the greatest risk of economic hardship after an HIV diagnosis. In the ≥ 40 age groups, which capture the age range of 45 and older, AIDS cases have increased steadily from 30.9% of the total cases diagnosed between 1981 and 1987 to 41.8% of the total cases diagnosed between 1996 and 2000. The increasing incidence and prevalence of HIV/AIDS among older people are likely to continue into the future because of a number of factors. HIV disease in older adults mostly stems from sexual behavior and this aspect of their lives needs to be addressed with older adults if further transmission of the virus is to be halted.
Archive | 2002
Janice E. Nichols; David C. Speer; Betty J. Watson; Mary R. Watson; Tiffany L. Vergon; Colette M. Vallee; Joan M. Meah
The chapter presents a case study of an individual infected by human immunodeficiency virus (HIV).. It illustrates a number of issues that have been raised while working with older people living with HIV disease (PLWHIV). It states that postdiagnosis, many older people are too often found forced to live their lives in a manner that differs greatly from the way they had planned—their reality often falls far short of the dreams toward which they worked throughout their careers. People who are considered to be middle-aged are often at the greatest risk of economic hardship after an HIV diagnosis. In the ≥ 40 age groups, which capture the age range of 45 and older, AIDS cases have increased steadily from 30.9% of the total cases diagnosed between 1981 and 1987 to 41.8% of the total cases diagnosed between 1996 and 2000. The increasing incidence and prevalence of HIV/AIDS among older people are likely to continue into the future because of a number of factors. HIV disease in older adults mostly stems from sexual behavior and this aspect of their lives needs to be addressed with older adults if further transmission of the virus is to be halted.
Archive | 2002
Janice E. Nichols; David C. Speer; Betty J. Watson; Mary R. Watson; Tiffany L. Vergon; Colette M. Vallee; Joan M. Meah
The HIV epidemic in the United States has heavily impacted people of color, particularly Blacks/African-Americans and Latinos/Hispanics. This chapter focuses on the impact of HIV disease on these groups, with major emphasis on the ways in which culturally competent outreach, prevention, and treatment programs can be designed to reach them. The chapter cites examples of strategies and programs that have been effective in reaching African-Americans and Hispanics. The primary reasons for the lower socioeconomic status (SES) of older African-Americans are patterns of limited employment opportunities and periods of unemployment throughout their lives. They have been concentrated in low-paying, sporadic service jobs with few benefits and no coverage by Social Security prior to the 1950s. The African-American participants in the survey project were found to be severely socioeconomically disadvantaged. The chapter addresses the barriers to effective outreach among African-Americans and the challenges associated with providing HIV-related services for Hispanic populations.Publisher Summary The HIV epidemic in the United States has heavily impacted people of color, particularly Blacks/African-Americans and Latinos/Hispanics. This chapter focuses on the impact of HIV disease on these groups, with major emphasis on the ways in which culturally competent outreach, prevention, and treatment programs can be designed to reach them. The chapter cites examples of strategies and programs that have been effective in reaching African-Americans and Hispanics. The primary reasons for the lower socioeconomic status (SES) of older African-Americans are patterns of limited employment opportunities and periods of unemployment throughout their lives. They have been concentrated in low-paying, sporadic service jobs with few benefits and no coverage by Social Security prior to the 1950s. The African-American participants in the survey project were found to be severely socioeconomically disadvantaged. The chapter addresses the barriers to effective outreach among African-Americans and the challenges associated with providing HIV-related services for Hispanic populations.
Aging with HIV#R##N#Psychological, Social, and Health Issues | 2002
Janice E. Nichols; David C. Speer; Betty J. Watson; Mary R. Watson; Tiffany L. Vergon; Colette M. Vallee; Joan M. Meah
The HIV epidemic in the United States has heavily impacted people of color, particularly Blacks/African-Americans and Latinos/Hispanics. This chapter focuses on the impact of HIV disease on these groups, with major emphasis on the ways in which culturally competent outreach, prevention, and treatment programs can be designed to reach them. The chapter cites examples of strategies and programs that have been effective in reaching African-Americans and Hispanics. The primary reasons for the lower socioeconomic status (SES) of older African-Americans are patterns of limited employment opportunities and periods of unemployment throughout their lives. They have been concentrated in low-paying, sporadic service jobs with few benefits and no coverage by Social Security prior to the 1950s. The African-American participants in the survey project were found to be severely socioeconomically disadvantaged. The chapter addresses the barriers to effective outreach among African-Americans and the challenges associated with providing HIV-related services for Hispanic populations.Publisher Summary The HIV epidemic in the United States has heavily impacted people of color, particularly Blacks/African-Americans and Latinos/Hispanics. This chapter focuses on the impact of HIV disease on these groups, with major emphasis on the ways in which culturally competent outreach, prevention, and treatment programs can be designed to reach them. The chapter cites examples of strategies and programs that have been effective in reaching African-Americans and Hispanics. The primary reasons for the lower socioeconomic status (SES) of older African-Americans are patterns of limited employment opportunities and periods of unemployment throughout their lives. They have been concentrated in low-paying, sporadic service jobs with few benefits and no coverage by Social Security prior to the 1950s. The African-American participants in the survey project were found to be severely socioeconomically disadvantaged. The chapter addresses the barriers to effective outreach among African-Americans and the challenges associated with providing HIV-related services for Hispanic populations.
Aging with HIV#R##N#Psychological, Social, and Health Issues | 2002
Janice E. Nichols; David C. Speer; Betty J. Watson; Mary R. Watson; Tiffany L. Vergon; Colette M. Vallee; Joan M. Meah
This chapter reviews sexual changes that take place during the aging process, cultural issues related to older-adult sexuality, and psychosocial matters that impact sexuality and vulnerability to infection. A survey conducted by Starr and Weiner (1981) concerning feelings about the sexual activities of older adults revealed that older people defined and expressed their sexuality in more diffuse and varied ways than did younger cohorts. Older people who lack knowledge about normal age-related changes in sexual functioning may adopt societal attitudes about sexual activity in later life, thus experiencing anxiety regarding sexual expression. The constraints that society imposes on the sexual freedom of older people are particularly evident in elder-care institutions. Older residents who display any form of sexual expression should not be regarded as having a behavioral problem, but as expressing a normal function of their sexuality. The institution has become their home and they should be afforded the privacy to engage in sexual practices. The chapter reviews the effects of the aging process on sexuality, along with some of the associations between older-adult sexuality and HIV disease.