Is it okay to lie to someone with dementia?

A person with dementia might ask questions that are difficult to answer truthfully without causing distress. Read our advice on why the person might be asking these questions and how to respond in situations where it might be better to lie or to not tell the whole truth.

I try not to lie, honestly, but some things push the boundaries: “Socks! You shouldn’t have”; “Oh, I thought you meant I should eat the entire cake” and – often to my subsequent regret – “No, I'd love to have your mother visit”.

Being a bit flexible with the truth is just part of the social contract, it seems - the price we pay for jogging along in relative peace. But what if one of us has dementia? What price comes with telling the truth then?

Types of questions a person with dementia might ask

The questions people living with dementia ask can challenge us. You may recognise some of these from your own experience:

  • When is dad coming to visit? (When the person’s father is sadly long dead)
  • Will I be going home soon? (Person living in a nursing home)
  • Shall I set the table for the guests? (From a former B&B owner, now in residential care)
  • You seem nice... but who are you? (Person to their partner)
  • Who are those little people by the window? (Person could be living anywhere)

For those close to people with dementia, how to respond to their questions can be a daily challenge. Is it acceptable to lie – ever? Or should we just tell the brutal truth - always?

How we respond will affect how the person and us feel and behave, now and in the future. We feel that if we get things ‘wrong’ we might damage a relationship that may well be already strained. 

Why might a person with dementia ask difficult questions?

Difficult questions often arise when the person is living in a different reality and/or has different beliefs from those around them.

These differences may become more apparent as dementia progresses but they are not limited to the condition’s later stages. They include:

  • behaving as a younger version of themselves (time-shifted)
  • beliefs – sometimes strongly held – that are false to others (delusions)
  • unfounded suspicions or allegations about others (infidelity, malice, deceit)
  • experiencing things that aren’t there (visual hallucinations).

We need to understand that these realities and beliefs often have meaning for the person with dementia, and we should not belittle or dismiss them.

Rather, as with changes in behaviour, the challenge when supporting someone is to get behind the words, rather than attribute them as simply dementia ‘symptoms’.  (Hallucinations in dementia with Lewy bodies may be an exception because they can be a symptom.)

For example, if someone with dementia asks for their dad, they may be expressing a need for comfort which is not being met.

If someone says they are setting the table for 'guests', maybe it's because they are looking for something to do, or are using older, more familiar memories to make sense of the present. When someone with dementia invents a story, it may be a coping strategy to support self-esteem.

When someone with dementia unknowingly invents a story – which is called confabulation – it may be a coping strategy to make sense of the world around them.

Should you always tell the truth to a person with dementia?

Is it important to recognise that 'truth' and 'lies' are not always simple or clear cut.

A spectrum runs from ‘whole-truth telling’ through ‘looking for alternative meaning’, to ‘distracting’, ‘going along with’ and finally ‘lying’.

As we move through this sequence the level of deception rises and we feel less at ease; who likes lying to a loved one?

It feels uncontroversial that we would all want our default response setting to be telling the whole truth. But it is equally obvious that the whole truth can sometimes be brutal or cause pain or discomfort. Who would support telling the whole truth when a person repeatedly asks after a long-dead parent as if the parent were still alive?

The whole truth here could mean repeatedly breaking the news of the parent’s death as if it has just happened, over and over again. What could be more cruel?

Selecting the correct response to reduce distress

We instinctively want to lean towards the ‘whole truth' end of the spectrum, but we also want to minimise any distress our response causes to the person with dementia.

But these aims often contradict, leaving us to seek a balancing act or a ‘least-bad’ trade-off. (We should not forget our own wellbeing either, as we don’t want to end up feeling bad about ourselves.)

One consequence of this approach is that we tell a direct lie only when doing anything else would cause the person significant physical or psychological harm. Professionals sometimes call this a ‘therapeutic lie’, but it needs to be seen a bit like antipsychotic drugs: used only under very select conditions and even then only with extreme care.

It’s also really important to recognise how hard this balancing act can be, and how impossible it can sometimes feel.  This is true particularly if the person’s realities/beliefs fluctuate – for example, if they are time-shifted only some of the time.

Carers can often find themselves being unfairly accused or argued with, find that their own reality is being suppressed, or feel unnecessarily guilty if they occasionally get their response ‘wrong’.

Responding to difficult questions from a person with dementia

Although every case needs taking individually, some guiding principles to start with include:

  • be compassionate 
  • try to understand and acknowledge the person’s feelings
  • seek to reduce distress and promote wellbeing or happiness.

When a person with dementia thinks you have stolen from them

Let’s take an example of a person who believes you stole their purse, on the assumption that the person’s suspicion is unfounded and they’ve simply mislaid it and forgotten where it is.

Perhaps this has happened before and when you found the lost purse you returned it with a whole truth: ‘I didn’t steal it; I found it in a drawer where you put it’. 

If this approach has caused an argument or distress, it may be better to try something less blunt next time: ‘It looks like it wasn’t stolen after all, it was just hiding upstairs’. If it’s a common accusation, trial-and-error can be useful in finding a suitable approach.

When a person with dementia asks about a deceased love one

If you think the person needs comfort or assurance, then ‘Is there something you wanted to speak with them about?’ might work.

The person with dementia may just want to reminisce about the person, and you could try saying something like, ‘I can tell you really cared for each other – tell me about them’, perhaps reinforced with personal photos, letters, or objects.

Or it may be that the person with dementia is still grieving, in which case gently acknowledging that their partner has died and supporting them to grieve might be best – for example by talking about their relationship and the person’s life.

As is so often the case for a person with dementia, feeling heard may be more important than being given advice.

But if the question here is frequent and the grief severe, then the kindest response is likely to be to acknowledge the person’s feelings and gently move them on to a topic or activity that you know they will enjoy. This is clearly ‘distraction’ but it should still not deny or ignore their feelings.

This article was first published in 2019 and most recently updated in February 2024.

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93 comments

What a lovely thing to say, 'love lies'. Of course you will tell porkies if that will ease the distress of your loved one. Common sense tells you that disturbing and making sad the one you love is simply not the thing to do.

Best advice in my opinion on dealing with dementia came in five words from Maureen Reagan, whose father former President Reagan developed Alzheimer’s. She said simply: “You go where they are.” And yes, having had a brother who died from Alzheimer’s, I know the truth of this remark. Of course you don’t try to inflict reality on them. Loving lies are allowed! Read the helpful “Contented Dementia” by Oliver James.

As a friend of a 91 year old living with alzheimers I often 'go along' with where she is at - it is much simpler for me and also more compassionate a response.
As she lives in a residential home but always wants to 'go home' I simply say "You are having your tea here today and staying the night here too, you will enjoy that"...…..we cope with the short term, the here and now.

Sadly my Gran suffered with dementia prior to her passing in 2015. Looking at the scale from truth to lying I can recognize various situations when we did all of this. For example, she consistently asked us when she was going home or why my mother (who was suffering with breast cancer) was poorly. We tried to be truthful to start with but quickly realized that it was causing more distress. It soon became apparent that distracting or lying was better for her wellbeing than being bluntly truthful. It does create a moral dilemma though - do you make them feel better but lie or do you tell them the truth knowing it will cause distress? At the beginning of the dementia journey with my Gran we used to challenge smaller issues we had like if she tried accusing someone or got confused about where someone was or what their name was. However, as it got worse, even the smallest issue caused a lot of distress and it soon was best for her wellbeing that we just distracted her from the issue or lied. It is an interesting dilemma though.

I had to have my mother's very much loved dog put to sleep as she was suffering badly from kidney disease. I chose the time when my mum was in hospital for a few days as by then, her dementia was so advanced that she would repeatedly ask the same questions. There was no way that I could break the news to my mum about her dog as every time the question 'where's Jenny?' would be asked, neither her carers or myself could inflict such cruelty on my mum and tell her she was dead. So we agreed a story: if my mum asked at night, the answer was 'Jenny's staying with Val tonight' and in the day, 'Ellen (her friend in the village) has taken her out for a walk.' It worked perfectly and my mum was happy with either answer. What could possibly have been gained by telling her the truth? I only found out about these 'love lies' through reading a book where a son's father kept asking where his wife was. The son kept saying 'but she's dead, dad.' Father was utterly distraught until the son changed his response to 'she's in Paris for the weekend dad.' Dad would then smile with delight and say' oh, she loves France, I'm so happy, she must be having a lovely time.'

I worked as live-in carer for a 92-year old gentleman who sometimes at meal times asked the whereabouts of his (deceased) brother. His wife's approach was to calmly and rationally explain to him that his brother had sadly passed away. And every time he reacted to the news as if it was the first time he was being told about it. Imagine going through the news of a loved one's death again and again. He would then doubt it - "surely I would remember my own brother's passing?" - and feel bad and confused over it until it eventually slipped away from his mind again.

My Mum frequently tells of places that she has been and we know she hasn't but we just smile and say really. I only ever contradict her if I absolutely have to. There is no need to make her feel bad.

My wife has mid stage Alzheimer’s and I do lie quite often. We may be passing a place we have never been and she will often comment about being there in the past and I just go along with it. I do this every time. It stops her becoming agitated.

I just wanted to say how really useful I found this article. Thank you

I found the previous comments very understanding and helpful. My partner has mid stage Alzheimer's.

I am prepared to defend a big lie. My 86 year old mother has had Alzheimer`s Disease for 4 years. As far as she is concerned,she has age related memory loss. I and my sister have Power of Attorney of her finances and her health. We made sure her affairs are in order,and make sure all professionals are aware that we do not use words like Dementia. We feel we have protected her and kept her spirits up by doing this.

Reality orientation always seemed cruel when I was nurse training in the 80’s and now having lived with loved ones with this awful disease I think theraputic lies necessary.

I cared for my wife for 9yrs and I admit telling a few porkies in that time. My wife frequently asked " when are children coming" really meaning the grand-children. It took a few minites but she never
forgot who I was.

My husband likes to go see his friends at the town bar. But when he stars drinking he drinks them like they are water and does not know when to stop. He thinks he only had one or two drinks. Anyone else have this problem?

Yes my husband does the same and always swears that he has only had two pints all night even though he has been out all night

My mum used to like a glass of wine on a Friday and Saturday night. Unfortunately with dementia, she thought every night was Friday and couldn’t remember how many glasses she had drunk. We tried hiding the wine but she just bought more... so we siphoned it off and replaced it with non-alcoholic juice. After a few months she forgot about the ‘wine’ altogether.

My Dad does the same. I have spoken to the bartender when we arrive in the pub and asked to replace 3/4 of the pint with non alcoholic beer. As his taste buds have changed this still tastes good. You could ask his friends to help in this. I suppose it is another ‘love lie’ but it means he can enjoy a drink socially without the after effects.

I clearly remember my first 'encounter' with Dementia. I was in hospital myself with a facial injury and concussion and there was a lady opposite me in the ward, on her own and clearly distressed. Having gone over to talk to her, I quickly became aware that something was not right ( I was not educated on Dementia at the time - that was my prompt to learn about it). I was trying to offer her some sort of 'comfort' in a distressing situation (hospital), despite, by this time having been told 'you won't get anywhere with her, she has Dementia'. But she did start to feel more at ease and then started telling me that we were on a coach trip to the seaside and were staying in a hotel. She was worried as she had forgotten her beach towel and little things like that. I did not want to plunge her back into distress with the harsh reality of the situation so I went along with her narrative and it calmed her distress.
Did I do right? I did not understand Dementia at that time but even with what I know now, I would say yes. How could I have swapped her pleasant trip to the seaside for the cold reality of hospital?
I do not know what happened beyond that as I was discharged before her.

Why would we subject our loved ones to additional angst and distress by being brutally honest. Surely we owe it to them to protect them from harsh and unwarranted facts, their emotional well being must always be paramount. Please common sense must prevail.

I find it difficult sometimes what to do for the best when mum who has dementia thinks I'm her husband and wants to know when I'm coming home. She also gets flustered and panicky whenever she can't find something. One evening last week she rang more than 30 times but after the first few occasions I didn't bother answering. Is this wrong?

I'm not an expert but I think what the article reflects is that there is no right and wrong in these situations. It sounds as if you didn't answer the phone after the first few times because you needed some space after doing what you could to try to support her. It's important to pay attention to your emotional needs, as this will help to prevent burnout and help you to keep supporting your mum in the longer term.