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I once heard a SNF worker say the best response is “tell me about your home.” And that you will often get memories from their childhood.
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Reply to Suzy23
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Bulldog54321 Jun 1, 2025
This is a good idea.
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This is a common thing for people with dementia, even if they are still in their own home and have lived there for years. To them "home" comes to represent their childhood home or another place where they felt comfortable, loved, and life made sense.

What to say depends on the situation. To "I want to go home", I typically respond with "I know, me too, me too" in a wistful longing tone. I'm 61 and love my current home, but I have nostalgia for my childhood home, so I can relate to the longing.

You can ask them to tell you about their home - was there a garden, a favorite hiding place, did they have any pets? You may hear some interesting stories, and by listening, you'll give them the gift of returning to their home through their reminiscence.

If they say "When can I go home?", I answer "I don't know, we will need to check with the doctor" or you try another track like "As soon as the city says it's ok" (if they had previously been told their house had a flood or mold, etc.)

Think about a situation your loved one can relate to, and blame the delay on an authority figure they respect like physical ailment -> doctor, house problem -> city inspectors, etc.

Try to keep the answer short and resist the urge to give a long explanation or reason. They are beyond being able to understand why they are where they are, but they are not beyond being able to argue, so avoid giving them reasons, That is just fuel for more arguing.

Change the subject or show them something that will grab their attention. My mom loves videos of baby animals or children.
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GigiL7 Jun 5, 2025
Thank you Dogwood63!
These are all good strategies, especially if your loved one is highly functioning! You are so right about invoking “authority figures.” I also email or call my sister’s doctors ahead of appointments so that they can also tell her in person why she needs to stay there. Her hearing them say she’s there so that they can “monitor” her condition and keep her “safe.”, is way more effective than me telling her. She now tells me that she has to stay put because of her doctor.

Another distraction if the weather is good, if your loved one enjoys ice cream, and is still able to leave home or a facility, is taking that person out for an ice cream! Something about going out and eating ice cream changes sadness to gladness, by breaking the routine. The “ice cream memories” are usually happy ones, and the stories you’ll hear! Even when we return to Memory Care, the good memories remain for a while.
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Going “home” is not always home. Home is often yearning for familiar. With time the new home becomes familiar and the smaller universe becomes comforting. It takes time but stick to it. Taking them out for visits actually makes it worse in my experience.
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Reply to Maurice53
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My dad has been asking to leave his MC facility for 2+ years. All you can do is keep agreeing and saying you know, try to change the perspective by talking about the positives there... "everyone is so nice, the food is really good"
And of course try to change the subject. My dad is extremely confused and cannot follow a conversation, but consistently asks to get out of this place.
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Reply to yungstdaughter
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Nothing. They want to go back to their childhood home.
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Reply to Bulldog54321
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Agree with Dogwood63. My mom has been in Memory Care Unit for a little over 2 months. She stills talks about “going home” or “getting out of here,” but not as frequently or as adamantly as she did the first several weeks she was there. Explaining that it was no longer safe for her to live at home alone did not work. Our standard response now is that she is there “for rehab” and that it is up to the doctors to determine when she is able to return home. While this may seem “dishonest” at first, it may help to remember that your loved one’s brain is not functioning properly now and that their brain cannot understand the current situation.
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Reply to Dementia5ux
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You have heard here how common this litany is to those in care, and that won't change, so the best advice would be to say the truth, that you are so very sorry, but that for her own safety going home isn't safe for her anymore.

You are, I think, perhaps thinking there is a way to "make this stop"? But there isn't. You will be asked this over and over. Every time she sees you she sees you as her only hope of escape. The less said the better. Just the simple truth. Over and over again.
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Reply to AlvaDeer
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Unfortunately everybody has the need to believe or hope that they will return to familiar surroundings ie. live in the home which has many memories
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Reply to carecallingnow
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I do not say anything. I use to try to explain why he ( dad) is in the best place. But it easier to just not respond.
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Reply to faithfulbeauty
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I simply ask "where is home" and depending on the answer I then try to discuss and/or redirect the best I can. He once said 136th Street and in our 55 years of marriage we never lived at an address even similar. I asked his older brother and learned that was where they lived as young boys. It is amazing the conversations we have had. His PD related dementia now has Lewy Bodies involved. He can no longer separate what is on TV from reality. If I realize he is talking about "home" on TV, usually saying something like that is where "they" live so we don't have to worry about what is happening there. As with most questions involving something on TV, I usually give a similar answer and he will answer with Oh, OK. He often feels he has to solve TV character's problems.
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