Skip to main content
. 2013 Nov;27(11):613–620. doi: 10.1089/apc.2013.0030

Table 1.

Barriers to Care Reported by Women of Color Living with HIV and Attending an Academic Infectious Diseases Clinic (N=164)

Barriers to Care No problem at all N (%) Very slight problem N (%) Somewhat of a problem N (%) Major problems N (%) Missing N (%)
The shortage of psychologists, social workers, and mental health counselors who can help me address mental health issues 129 (82%) 14 (9%) 9 (6%) 6 (4%) 6 (4%)
The lack of psychological support groups for persons living with HIV or AIDS 120 (75%) 21 (13%) 10 (6%) 10 (6%) 2 (2%)
Long distances to medical facilities and personnel 111 (68%) 18 (11) 27 (16%) 8 (5%) 0 (0%)
The lack of transportation to access services I need 120 (73%) 17 (10%) 16 (10%) 11 (7%) 0 (0%)
The lack of employment opportunities for people living with HIV or AIDS 87 (55%) 14 (9%) 37 (24%) 19 (12%) 7 (4%)
The lack of supportive and understanding work environments for people living with HIV or AIDS 77 (50%) 16 (10%) 38 (25%) 24 (15%) 9 (5%)
Lack of adequate and affordable housing 91 (56%) 23 (14%) 28 (17%) 20 (12%) 2 (1%)
Breaches of confidentiality 105 (64%) 17 (10%) 19 (12%) 23 (14%) 0 (0%)
The level of knowledge about HIV or AIDS among people in the community 91 (56%) 14 (9%) 33 (20%) 24 (15%) 2 (1%)
My personal financial resources 73 (45%) 22 (13%) 39 (24%) 30 (18%) 0 (0%)
Community residents' stigma against persons living with HIV or AIDS 71 (44%) 26 (16%) 31 (19%) 35 (21%) 1 (1%)