“…With regards to informal carers of HIV/AIDS patients in particular, as in our case, first and foremost, information needs will relate to the diagnosis and the progression of the condition (Selman et al, 2009), i.e., information on how the disease might affect the cared for person over the longer term (Ogden et al, 2006). In addition, because of the nature of the particular condition, the information needs will cover aspects of access and dispensation of antiretroviral (ARV) therapy, nutrition, including managing stress (Mnubi-Mchombu et al, 2009), recognising and managing the symptoms of HIV/AIDS (Gysels et al, 2011) and of comorbidities that often affect HIV/AIDS patients, productive and reproductive activities (Asuquo et al, 2017), among others. However, as the condition and the circumstances of both the carer and the cared for person are likely to evolve over time, the information needs are also likely to evolve (Larkin et al, 2019).…”