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What Works for Women and Girls

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6. Support groups <strong>for</strong> people living with HIV may reduce stigma. [See also Chapter 7. Treatment]Following violence in Kenya, VCT services were established, with counseling <strong>and</strong> accessto antiretroviral therapy <strong>for</strong> those who tested HIV-positive. Support groups <strong>for</strong> 100women <strong>and</strong> 45 men living with HIV had reduced stigma. Along with ART, nutrition iskey to supplement relief ef<strong>for</strong>ts (Wambete <strong>and</strong> Ptoch, 2008). (Gray V) (violence, counseling,testing, support groups, antiretrovirals, nutrition, Kenya)7. Support to voluntarily disclose positive serostatus, <strong>and</strong> continued support, increasesHIV-positive women’s ability to cope <strong>and</strong> access treatment regimens <strong>and</strong> reduces perceivedstigma in the community.A study carried out from 1999 to 2001 in Thail<strong>and</strong>, with 329 HIV-positive women foundthat HIV-positive women who reported that they could disclose their HIV serostatusgained increased acceptance <strong>and</strong> support from family <strong>and</strong> community, accessed supportgroups that increased their ability to cope with the disease, <strong>and</strong> increased their access totreatment regimens. Of the 329 women, 57% participated in one or more HIV-positivesupport groups. One woman stated: “At that time, when I knew I was HIV-positive, Ithought, how could I live! Then, I had a chance to learn about a support group. I joinedthis group. I feel good cause I can meet others who’re the same as me...” (p. 37). Anotherstated: “I can get more knowledge from others who have had the same experiences. Ifeel that there are many people living with HIV, not only me. I feel warm when I joinin the group” (p. 37–38) One woman stated: “In the village, everybody knew my HIVstatus. At first, they did not accept me, but now they have a good relationship withme. I can eat <strong>and</strong> talk with them. I think that I can live well in the village” (p. 37). Thewomen were interviewed using a structured questionnaire. In-depth interviews wereconducted among 60 HIV-positive women. Four participatory workshops were held ondata analysis <strong>and</strong> report writing. A week long counseling training session was held <strong>for</strong>the women conducting interviews. <strong>Women</strong> interviewed were selected non-r<strong>and</strong>omlyfrom support groups, clinics, ANC clinics, NGOs, <strong>and</strong> communities using dimensionalsampling method. The dimensions used were ages 15–25, 26–35, or 36–49, <strong>and</strong> numberof years from diagnosis. <strong>Women</strong> who met the criteria <strong>for</strong> both dimensions were selectedbased on convenient or snowball sampling techniques. Six focus group discussionswere held with six to eight men (Yoddumnern-Attig et al., 2004). (Gray IV) (stigma,discrimination, disclosure, Thail<strong>and</strong>)A qualitative study of interviews with 75 HIV-positive people (43 females, 32 males)from 20 countries, including Australia, Botswana, India, Kenya, South Africa, Thail<strong>and</strong>,Ug<strong>and</strong>a, Zambia, <strong>and</strong> Zimbabwe, conducted between 1997 <strong>and</strong> 1999, found that immediatelyfollowing diagnosis, most respondents felt shame <strong>and</strong> a sense of worthlessness.Most carefully guarded the secret of their serostatus <strong>for</strong> fear of negative repercussions.The average time between diagnosis <strong>and</strong> public disclosure was 2.6 years, as most peopleneeded to time to talk through their fears with peers or a counselor. Motivation <strong>for</strong>WHAT WORKS FOR WOMEN AND GIRLS335

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