When Someone
With Dementia Says:
"I Want to Go Home"
One of the hardest things
is to hear someone with Alzheimer’s or another dementia to say "I
want to go home.” After this major question others more practical will follow.
"Where's my purse? Have we paid yet? Should we take a bus? Do you know
where can I find a bus pass? I feel better so why we don’t go home?"
Most of the residents
cannot accept the fact that they are living in care homes. They believe that
they are in hospital/institution, in prison or somewhere else. They don’t
recognize or they don’t want to accept that the care home is their new home.
"I want to go
home" isn't usually meant literally by someone with moderate or late-stage
Alzheimer's. It’s the memory that missing and not the actual home.
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.
One of the residents in a care home in America, was referring to "going
home pretty soon," The family later have 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 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 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
Home is where the heart is. Dementing illnesses strip safety away. Little by little and sometimes in large chunks the familiar becomes unfamiliar. The little things a person unconsciously counts on to clue them in to where they are, who they are, how they should act and what they should expect disappears. Home is the place where I don’t have to worry, where I can rest, relax, breathe deeply and know everything is alright.
Unfortunately, when you are
losing your mind everything is NOT alright no matter what anyone says to
convince you otherwise.
Families resort to all kinds of tricks to deal
with this and sometimes that works. Sometimes going for a drive around the
block and going through the familiar action of walking up to and opening the front door to
one’s house is enough to trigger the feeling of “at home” for a confused
patient. An old favorite dessert or a piece of music can do the same thing.
But when all else fails—the
usual tricks, the false reassurance, the distractions—it’s time to get honest.
Things aren’t the same anymore. Neither one of
you is in familiar territory anymore and it does feel terrible.
But home isn’t just where
things feel familiar. “Home is where they have to take you in.” “Home is where
everyone knows your name.” Home is where you know you are loved.
Remind the patient
(and yourself) that you still have love, the ability to show you care and the
ability to receive it. Even the most demented patient is capable of holding
your hand and vice versa. So hold hands together, be together and claim a
moment of comfort.
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.
What does “home” mean?
What
if dementia means you never feel like you are at home? Home is not just a
physical place, but an emotional and spiritual one. If home is a place filled
with your memories and hopefully a feeling of safety and with dementia you are
losing your memories and everything feels unsafe, maybe there is no place you
can call "home." Maybe when someone with dementia says "I want
to go home" they may be telling us how unsure they are of life and
everything they once knew.
- Home could mean one’s birthplace
- Their childhood home
- A relatives home where memorable events took place
- The home where their children were raised
- Their most recent home
- The job they so loved
- Home as in Heaven
- A change as in state of mind
- Take me away from the noisy TV or music
- Take me to my room where it’s quiet
- Take me to that place where I feel safe
- Take me to that place where I feel loved
VALIDATION THERAPY
A very
popular form of conversation with dementia persons is the use of a program
called validation therapy. The idea behind validation therapy is to
"validate" or accept the values, beliefs and "Reality" of
the dementia person - even if it has no basis in your reality.
Here is an example of how a validation therapy
conversation might work.
John: "I
have to find my car keys."
Me: "Your car keys..." ( I don't tell him he doesn't have a car or he hasn't driven for years)
John: "Yes, I need to get home - lot's of work to do, you know!"
Me: "Your car keys..." ( I don't tell him he doesn't have a car or he hasn't driven for years)
John: "Yes, I need to get home - lot's of work to do, you know!"
Me: "You
are busy today?" (I don't tell him that is flat has been sold)
Or
Mary: I want to go home!
Me: Who is home? (I am not saying
this is your home)
Mary: My mum and she is waiting for
me.
Me: What’s your mother’s name? (I am
not saying your mother is dead)
The key is to
"agree" with what they want but by conversation and "steering"
get them to do something else without them realizing they are actually being
redirected. This is both validation and redirection therapy.
Does this always
work? NO! But it has a pretty high success rate because it is so
non-confrontational. If you can avoid direct confrontation, you will be much
happier and so will the dementia person. I know that sometimes a direct
confrontation is needed; but I see those confrontations occur far more often
than they need to.
Does knowing this make hearing
"I want
to go home" any easier?
I hope so.
Eirini Dermitzaki (Activities
Cordinator)
Sources:
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