This essay analyzes dementia healthcare delivery in Australia, examining various healthcare models like primary and tertiary services, and their underpinning values. It explores the impact of social determinants of health, particularly poverty, on dementia outcomes, highlighting how it affects access to services and increases vulnerability. The essay emphasizes the significance of cultural safety and person-centered care in improving patient engagement and outcomes. It critiques instances of discrimination and stigma within healthcare, referencing ethical codes and standards, such as the International Council of Nurses Code of Ethics and the NSQHS standards, and stresses the need for nurses to cultivate empathy and cultural sensitivity. The analysis underscores the disproportionate burden of dementia on elderly and female populations and the importance of addressing negative attitudes towards patients to enhance care and support.