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Abstract \nPoints of Interest The aim of this paper is to explore everyday life experiences of migration and disability from an intersectional perspective drawing on issues such as gender, class, and ethnicity. This is relevant because when focus is on either migration or disability, unique challenges faced by disabled migrants are neglected, leading to fragmented support and a lack of accurate knowledge. The analysis is based on retrospective data from photovoice sessions conducted within the context of a community-based project, Disabled Refugees Welcome (DRW). A secondary analysis has involved eight of the members from the original photovoice sessions as well as academics. The results are presented in a narrative thematic analysis. The findings show how the combined effects of liminality, structural violence (lack of accessible and adapted housing, lack of access to knowledge about societal resources), and multiple discrimination risks can result in permanent exclusion.Exploring the implications in everyday life about issues related to migration, gender and disability is necessary to raise awareness of assumptions and stereotypes, which can improve health and living conditions for disabled migrants.Current guidelines and laws insufficiently provide guidance and support for disabled persons who are also migrants.Education, work, housing, and healthcare are critical parts for inclusion in northern. European societies, yet too often inaccessible for disabled migrants.Experiences of disability and migration can amplify feelings of loneliness, inadequacy and isolation. [ABSTRACT FROM AUTHOR]

People with dementia have typically been treated as homogenous groups with little recognition of unique aspects of identities, including age and gender. The purpose of this paper is to illuminate the experiences of women living with young onset dementia which led them to take up advocacy roles as a result of their experiences. Five women from Canada who were diagnosed with young onset dementia and had then taken on advocacy roles were interviewed. Two main themes emerged–Moving In (the challenges of a diagnosis) and Moving On (into a new life). They described the challenges of a diagnosis as stopping work, being taken seriously, fighting for support, failing to meet requirements for programs and services, and changing relationships with friends. The challenges led them to move into a new life, accepting their diagnosis, and moving into new roles of advocacy and supporting others with dementia in their journey. Further research should seek to explore diversity, rather than treating people with dementia as the same. The experience of dementia is different for everyone. From getting a diagnosis to living a life with dementia, these experiences are unique. Based on interviews with five women living with dementia diagnosed before age 65, it was found that the challenges of getting a diagnosis led the women to become advocates for supporting others with dementia in their journey. The challenges of a diagnosis included stopping work, being taken seriously, fighting for support, not meeting requirements for programs and services, and changing relationships with friends. As a result of their experiences, the women moved on into a new life, accepting their diagnoses, and taking on advocacy roles to create change for others living with dementia. The advocacy roles undertaken by these women demonstrate the need to recognize the unique aspects of people with dementia, in particular women with young onset dementia, without making assumptions that the experience of dementia is the same for everyone. [ABSTRACT FROM AUTHOR]