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What strategies have you found most effective in communicating complex medical information to families?
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How do you currently assess the needs of caregivers when discussing care options for dementia patients?
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Can you share an experience where a community resource significantly helped a family in your care?
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What challenges do you face when comparing different care settings for families?
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How do you incorporate cultural sensitivity into your discussions with families about dementia care?
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What tools or resources do you wish you had to support caregivers better?
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How do you approach financial discussions with families regarding care options?
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What community-based interventions have you found most beneficial for caregiver support?
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How can we improve the way we present facility checklists to families evaluating care options?
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What feedback have you received from families about the educational materials you've provided on dementia progression?
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