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Abstract

The multiple stressors associated with caregiving for someone living with Alzheimer’s Disease and Related Dementias (ADRD) often place enormous burdens on care partners. To better understand the caregiving-related needs and priorities of people with lived experience as care partners of people living with ADRD, focus groups were convened with care partners who identify with historically and currently underserved communities who may have difficulty accessing culturally-specific services for people living with ADRD in and near the Portland, OR metropolitan area.

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