When Someone With Dementia Says, “I Want to Go Home”

by Paula Spencer

One of the hardest things to hear someone with Alzheimer’s or another dementia say is, “I want to go home.”

I used to dread the moment near the end of a visit with my Gram (who had Alzheimer’s) when she’d perk up from a semi-stupor in which she no longer recognized me:“Where’s my purse? Have we paid yet? Let’s go home.”Briefly, she sounded almost like her jolly old self.

No matter how long I was there, or what we did, it ended like a perpetual restaurant outing. Except of course that she lived at this “restaurant.”

I’ve since learned that “I want to go home” isn’t usually meant literally by someone with moderate or late-stage Alzheimer’s, nor should it be taken that way. Some things I’ve learned:

  • Don’t argue, “But you are home!” For one thing, the “home” being spoken of may not be the same place you’re thinking of. When my father refers to “going home pretty soon,” for example, we’ve learned that he doesn’t mean the house where he lives now or the town where he lived for 40+ years. He’s referring to far-away Upper Michigan, his birthplace, where he hasn’t lived since college. His long-term memory and emotions have conspired to have made that place the representation of a feeling of deep security.

Arguing with someone with dementia, as you already know, is counterproductive.

  • Hear “home” as a feeling you need to read. When people with mid- or late-stage dementia who live in a facility or are hospitalized say, “I want to go home,” what they’re really saying is, “I’m uneasy,” or “I’m scared.” To all of us, the very concept of home is a mood that’s soothing, familiar, and safe. Doesn’t matter whether the “home” in the person’s head is a childhood home, the home where they raised their family, or the place they live now – or all of them co-mingled as a just particular, satisfying kind of feeling, rather than a place.
  • Don’t be overly distressed. Hearing “I want to go home” can provoke lots of emotions in family members: Worry that “she hates it here.” Guilt at having placed her there. But remember that by mid-stage Alzheimer’s, the person is not very capable of manipulating you, if for no other reason than within a short time she will have forgotten what she said (unless you provoke and prolong by arguing over the geography of home).
  • Go along to get along. “A fib-let is better than a tablet.” Too often, the person is told, “This is your home now,” and their underlying emotional need goes unaddressed. The person grows more distressed — and then is often medicated to calm down.

Better: Give a hug. Meet that emotional need (fear, uncertainty). Be positive, not negative: “The weather’s too bad to go out now, maybe later.” Or, “Why don’t we listen to some music first?” Shift the attention to a happier ending.

I try to keep in mind the more-true-than-I-knew adage, Home is where the heart is.

Does knowing this make hearing “I want to go home” any easier? I hope so.

Advertisements

Leave a comment

Filed under adult children of aging parents, Adult day care, Alzheimer's Disease, anxiety and the elderly, assessments, care giving, care planning, caregiving, clinical trial studies, dementia, Depression and the elderly, elder care raleigh nc, employee stress, Geriatric Care Management, Long Term Care Insurancee, long term care planning, NC, Nursing Homes, nursing homes and assisted living, paying for home care, Raleigh, respite, senior care, Seniors and driving, sibling relationships, support groups, travel with seniors, Uncategorized

Leave a Reply

Fill in your details below or click an icon to log in:

WordPress.com Logo

You are commenting using your WordPress.com account. Log Out / Change )

Twitter picture

You are commenting using your Twitter account. Log Out / Change )

Facebook photo

You are commenting using your Facebook account. Log Out / Change )

Google+ photo

You are commenting using your Google+ account. Log Out / Change )

Connecting to %s