social context of disclosing hiv test results: hiv testing in tanzania
social context of disclosing hiv test results: hiv testing in tanzania
social context of disclosing hiv test results: hiv testing in tanzania
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5.5 Problems and Challenges <strong>of</strong> HIV Test<strong>in</strong>g<br />
Although HIV <strong>test</strong><strong>in</strong>g through VCT is becom<strong>in</strong>g <strong>in</strong>creas<strong>in</strong>gly available <strong>in</strong><br />
Tanzania, many people are still reluctant to be <strong>test</strong>ed, for they fear discrim<strong>in</strong>ation. As two<br />
ladies said:<br />
My mother started to <strong>in</strong>form other people that I was HIV positive even<br />
before I was <strong>test</strong>ed. She even told my children that their father who<br />
recently died was HIV positive and that they should look somewhere else<br />
when I die.<br />
These f<strong>in</strong>d<strong>in</strong>gs are similar to f<strong>in</strong>d<strong>in</strong>gs that have been reported by other studies that<br />
have shown that <strong>in</strong>dividuals avoid gett<strong>in</strong>g <strong>test</strong>ed for fear <strong>of</strong> <strong>in</strong>appropriate HIV screen<strong>in</strong>g<br />
without consent and counsell<strong>in</strong>g, fear <strong>of</strong> learn<strong>in</strong>g that one is HIV positive, fear <strong>of</strong> a<br />
partner’s reaction, belief that one is unlikely to be exposed to HIV, and many others<br />
(Fako, 2006; Campbell and Bernhardt, 2003; Burns et al., 2004; Isezuo and Onayemi,<br />
2004; Peltzer et al., 2004; Gage and Ali, 2005). Because fear <strong>of</strong> rejection or stigma is a<br />
common reason for avoid<strong>in</strong>g <strong>test</strong><strong>in</strong>g, l<strong>in</strong>k<strong>in</strong>g <strong>test</strong><strong>in</strong>g with ongo<strong>in</strong>g care and support<br />
services, as well as HIV education and awareness <strong>in</strong> the community, can reduce stigma<br />
and may contribute to wider acceptance <strong>of</strong> VCT.<br />
As far as challenges are concerned, there is a need to <strong>in</strong>crease accessibility to<br />
VCT, expand the build<strong>in</strong>gs for VCT to promote privacy and ma<strong>in</strong>ta<strong>in</strong> confidentiality,<br />
<strong>in</strong>crease awareness, and monitor the quality <strong>of</strong> counsell<strong>in</strong>g. Confidentiality and privacy<br />
are the ma<strong>in</strong> fundamentals <strong>of</strong> counsell<strong>in</strong>g. Therefore, confidentiality must be strictly<br />
observed as far as possible with<strong>in</strong> the counsell<strong>in</strong>g sett<strong>in</strong>g, which may <strong>in</strong>clude cocounsellors<br />
or assistants. The counsell<strong>in</strong>g should also be done <strong>in</strong> private. This calls for<br />
expand<strong>in</strong>g the build<strong>in</strong>gs for VCT to promote privacy and ma<strong>in</strong>ta<strong>in</strong> confidentiality. We<br />
shall discuss more issues that relate to challenges and problems <strong>of</strong> VCT <strong>in</strong> the next<br />
chapter.<br />
5.6 Conclusion<br />
In this chapter we have shown that there are many circumstances that compel<br />
people to take an HIV <strong>test</strong>. By look<strong>in</strong>g at the circumstances and reasons that made them<br />
take an HIV <strong>test</strong>, we noted that these respondents fall <strong>in</strong>to two dist<strong>in</strong>ct groups: those who<br />
got <strong>test</strong>ed because they were experienc<strong>in</strong>g poor health, and those who got <strong>test</strong>ed because<br />
<strong>of</strong> other reasons. For those whose health condition was poor, respondents were seek<strong>in</strong>g<br />
explanations for their chronic illnesses and a hope <strong>of</strong> antiretroviral drugs that could<br />
prolong their lives. Those who appeared healthy were motivated by their worries about a<br />
family situation like death <strong>of</strong> a sexual partner, chronic illness <strong>of</strong> a sexual partner, or<br />
concern <strong>of</strong> <strong>in</strong>fidelity <strong>of</strong> a spouse or sexual partner. We have also argued that although<br />
there are respondents who made decisions to get <strong>test</strong>ed <strong>in</strong>dividually, many respondents<br />
stated that they discussed the idea <strong>of</strong> <strong>test</strong><strong>in</strong>g with family members, relatives, neighbours,<br />
or friends, and that they weighed many factors before decid<strong>in</strong>g to get <strong>test</strong>ed. What this<br />
means is that HIV <strong>test</strong><strong>in</strong>g is not a technical process isolated from <strong>social</strong> factors, but it is<br />
above all a <strong>social</strong> process. The process starts by an <strong>in</strong>dividual mak<strong>in</strong>g the decision to be<br />
<strong>test</strong>ed or discuss<strong>in</strong>g his or her health problems or worries with other people, then he or<br />
she accesses <strong>test</strong><strong>in</strong>g services, undergoes counsell<strong>in</strong>g, takes the <strong>test</strong>, and waits for the<br />
<strong>results</strong>.<br />
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