Caring for someone with dementia can be physically and emotionally challenging and it can have a negative impact on the social, psychological and physical well-being of the carer (Ferrara et al., 2008;Richardson et al., 2013). This results in family carers of people with dementia often having high levels of physical burden and psychological distress (Collins & Kishita, 2020; Kaddour & Kishita, 2019). Therefore, exploring family carers' specific needs is critical, as this information can lead to the successful planning and delivery of community services and care plans, to the referral of carers to appropriate support and resources and to design research programmes and interventions to improve carer outcomes (Novais et al., 2017).Recent comprehensive systematic reviews on the needs of informal carers of people with different types of dementia demonstrated that the most explored topics of carer's needs in the literature were: information on the disease, support for the carers from others, coping with caring and behavioural symptoms, support from community services related to patient care (Bressan et al., 2020;Novais