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HamletInExile1 karma

(Resubmitted) I am an activity director in an assisted living community that has a memory care unit. We don't have a policy per se not to accept residents with advanced Lewy Body's but it has not been a good fit for us. We simply aren't staffed to give residents with LBD the kind of continual one on one attention they can need. Have thought about your care for later in the disease? Have you made plans? Is if there is anything you'd like your future caregivers to know? How do you wish caregivers would respond during an hallucination? By the time I've encountered residents with LBD, they could not tell me these things.