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What dementia care partners say they need

I asked dementia care partners what would help them reduce stress and improve their ability to provide care

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They said they needed more help (i.e. people), more breaks, more support, more visits from friends, more money. See the short answer here:  

What is a provocation or insight that might inspire others during this challenge?

The end users are the experts. Why don't we ask them what they need and then supply it?

Tell us about your work experience:

Primary care partner for ten years to my mother who lived with dementia. Blogger. Dementia care advocate. Research collaborator. My blog is here:


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