Tag Archives: lewy body dementia and aggression

Riding the Waves of Dementia

The extremes of Mom’s lewy body disease have lent plenty to write about lately, but making the time and space to emotionally process and translate it for others has not been something I’ve done.  Some if it still feels too … Continue reading

Posted in advocacy, dementia, lewy body dementia, memory care and residential options, parkinson's | Tagged , , | 2 Comments

Nowhere to Go

My mother has been in the hospital what seems like most of the summer, though I know it’s not true. This is her second hospitalization for the season, and I think we’re on week 3.  Anyone who’s a caregiver knows … Continue reading

Posted in advocacy, caregiver stress, support, and respite, dementia, doctors and medical, family issues, inclusion, lewy body dementia, memory care and residential options, parkinson's | Tagged , , , , | 3 Comments