The project's main OBJECTIVE was to improve the well-being of people living with dementia and their caregivers, creating an environment where all, including people with dementia, caregivers, and communities in general, could be better prepared to address the overall care needed for a better quality of life. To this end, a set of SPECIFIC OBJECTIVES was defined to address the NEEDS of the target groups, including the general public, communities, caregivers, caretakers, and entities in social care and welfare: Increased dementia awareness, inclusion, and friendliness Reduced risk of dementia Improved diagnosis and care Support for dementia caregivers Enhancement of health information and care systems for dementia Promotion of research and innovation
Dementia is a progressive cognitive impairment leading to declines in memory, thinking, and daily functioning. Alzheimer's is the most common type, affecting around 70% of cases worldwide. The WHO estimates 48 million affected globally, projected to triple by 2050. Population ageing, especially in southern Europe, drives its prevalence. Informal caregivers, primarily women, provide 80% of care, but intensive caregiving leads to reduced workforce attachment, poverty, and mental health issues. EU countries implement policies to support caregivers, such as Spain's National Plan on Alzheimer's. Stigma and lack of awareness hinder diagnosis and care, posing significant social and economic barriers if unaddressed.