The “Right to Know” or “Know Your Rights”?
Human rights abuses fuel vulnerability to HIV infection and act as barriers to universal access to prevention, treatment, and care. This has been recognized in numerous international declarations, and attention to human rights has been incorporated into the mission statements and work plans of grassroots groups and global organizations alike. Yet how recognition of this relationship is translated into action varies. This explores different contexts in which the claim of one particular right, the “right to know,” has emerged, and how this claim relates to the experience of people living with HIV. The “right to know,” defined variously and used to advance competing and controversial agendas, is then contrasted with efforts encouraging individuals to “know their rights.”