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Immigration trends and the increasing numbers of older adults with Alzheimer’s disease and related dementia (ADRD) have increased the demand for transnational care. While immigrant caregivers play a crucial role in providing essential support for individuals with ADRD, little is known about their needs and challenges. Semi-structured in-depth interviews were conducted with 32 transnational caregivers of parents diagnosed with ADRD. The analysis yielded four major themes concerning the caregiver experience: lack of care-related knowledge, judgment from family members and healthcare professionals, disruption of original daily routine, and loneliness. The findings will provide a basis for developing targeted interventions for transnational caregivers.

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