Advice
‘I want to go home’ - What to say to someone with dementia in care
Here are some ways family members and primary carers can approach the difficult question, 'What do I say to someone with dementia in residential care who wants to go home?'
It's not uncommon for a person with dementia to say they want to go home. This may be caused by time-shifting or general confusion, and can be distressing for everyone.
Below are a few considerations on what to say to someone in this situation who wants to go home.
5 things to remember when someone with dementia is asking to go home
1. Avoid arguing about whether they are already ‘home'
For a person with dementia, the term 'home' may describe something more than the place they currently live. Often when a person with dementia asks to go home it refers to the sense of ’home’ rather than home itself.
‘Home’ may represent memories of a time or place that was comfortable and secure and where they felt relaxed and happier. It could also be an indefinable place that may not physically exist.
It’s usually best not to try to reason or disagree with the person about where their home is.
If they don't recognise their environment as 'home' at that moment, then for that moment, it isn't home.
Try to understand and acknowledge the feelings behind the wish to go home. Find out where 'home' is for them - it might not be the last place they lived. It could be where they lived before moving recently or it could be somewhere from their distant past.
Often people with dementia describe 'home' as a pleasant, peaceful or idyllic place where they were happy. They could be encouraged to talk about why they were happy there. This can give an idea as to what they might need to feel better.
2. Reassure them of their safety
The desire to go home is probably the same desire anyone would have if we found ourselves in an unfamiliar place.
Reassure the person verbally, and possibly with arm touches or handholding if this feels appropriate. Let the person know that they are safe.
It may help to provide reassurance that the person is still cared about. They may be living somewhere different from where they lived before, and need to know they’re cared for.
3. Try diverting the conversation
Keep a photograph album handy. This could be a physical book or photos on a tablet or smartphone. Sometimes looking at pictures from the past and being given the chance to reminisce will ease the person’s feelings of anxiety.
It might be best to avoid asking questions about the pictures or the past, instead trying to make comments: 'That looks like Uncle Fred. Granny told me about the time he....'
Alternatively, you could try shifting the person's focus from home to something else - such as food, music, or other activities, such as going for a walk.
4. Establish whether or not they are feeling unhappy or lonely
A person with dementia may want to 'go home' because of feelings of anxiety, insecurity, depression or fear.
Think about whether the person with dementia is happy or unhappy when they mention going home. If they are unhappy, it may be possible to discover why. If they cannot tell you why, perhaps a member of the staff or another resident knows why.
Like anyone, someone with dementia may act out of character to the people closest to them as a result of a bad mood or bad day.
Does the person with dementia keep talking about going home when people are not visiting them in the care home? Does he or she seem to have settled otherwise? Ask the staff in the home as they may know.
5. Keep a log of when they are asking to go home
Certain times of the day might be worse than others. What seems to be the common denominator about these times? Is it near meal times (and would a snack perhaps help)? Is it during times when the environment is noisier than usual? Is it later in the day and possibly due to ‘sundowning’?
If you see a pattern, you can take steps to lessen or avoid some of the triggers.
This article was first published in 2018 and most recently updated in January 2024.
How can dementia change a person's perception?
People with dementia experience changes in how they perceive things. This includes misperceptions and misidentifications, hallucinations, delusions and time-shifting
Maryanna larsen
saysWhat would one do if person doesn’t speak ?
Hi Maryanna,
It can feel very difficult when dementia causes problems with communication. We have advice on all aspects of communication including when someone doesn’t speak: https://www.alzheimers.org.uk/about-dementia/symptoms-and-diagnosis/sym…
Our online community Talking Point includes many members with relatable experiences who can offer helpful suggestions and reassurance: https://www.alzheimers.org.uk/get-support/dementia-talking-point-our-on…
You might also want to speak with one of our dementia advisers, who can answer questions on the challenges of dementia. You can call our support line on 0333 150 3456, or find out more information, including opening hours, here: https://www.alzheimers.org.uk/dementiaconnect
We hope this helps, Maryanna.
Alzheimer's Society blog team
Shelby
saysSorry i realised i didn't really describe what he actually does lol
I feel he comes obsessed almost to the point that's all he fixated on problem is others start paying attention when he does these thing's.
He originally was removing the batteries out of the remote of tv and house phone we got to the point we couldn't keep going in circles so we glued the back of house phone, where it still charges etc, then came the prank calls which only way to prevent is ignore which is hard as worried he may need us also we was informed he made an few to people in his village stating he was lonely and wanted to talk but this scared me as I felt he may be putting himself in potential danger. At the minute his new fixation is he is uncomfortable, in pain and needs the carer's back out, unfortunately his other child did ring carers several time's for him , we refused after asking him why did he need carer's explaining its not an emergency, we have considered pretenting we have called them saying they can't come out but we believe this could potentially lead to difficulties with his carer's which isn't fair, however since his other child is also refusing he is ring emergency services where he has the ambulance atleast once but as much as 4, he also had the police at one point due to how many calls he is making, even though we have tried to explain and he seems to get the concept of what we are saying I'm not sure if he fully understands, he also refers to them as his carer's. I know most of this is him reacting to attention he receives and i can fully understand why he does it it is what most of us would do, we feel extremely guilty we aren't able to care for him but we just don't know what to do to help him as he isn't really helping himself and even calling him hourly and visiting him everyday which we couldn't keep up hasn't prevented this.
Hi Shelby,
We're really sorry to hear about your father-in-law, and how difficult this time has been for you and your partner.
Please know that you, or your partner, can contact our Dementia Connect support line on 0333 150 3456. When you call, our advisers can offer you detailed information, advice, and emotional support specific to your father-in-law's situation, as well as support for the two of you. More details about the support line (including opening hours) are available here: https://www.alzheimers.org.uk/dementia-connect-support-line
You might also benefit from joining our online community, Talking Point, where carers and other people affected by dementia share their experiences and offer support. This could be a great place for you to speak to and get advice from others who have been in similar situations: https://www.alzheimers.org.uk/get-support/dementia-talking-point-our-on…
We hope this helps, Shelby. Remember that you can always call our support line.
Alzheimer's Society blog team
Shelby
saysThank you very much appreciated.
Shelby
saysI want to apologise now as I'm not the best at writing where things make sense. I really don't want to sound selfish but we are struggling to know what to do with my father in law. Me and my partner both have extra needs i myself has Autism, ADHD, CPTSD and my partner has moderate learning difficulties. My father in law is such an genuine gentle soul and he is amazing for what he has done in his life especially for the years I've known him he gave up his life to look after his wife who unfortunately passed away in December just gone since then everyone in his life seems to have an reason not to want to know him, even though he was always pushed to the side too much in mine and my partners opinion as he would refuse his hospital treatment and this was acceptable in eyes of his other child as his wife had an personality disorder where she would be unbearable to the point he couldn't leave the home without her playing up. We was told there was no help and support for us as my father in law is deemed not an danger but some would be available if he gets diagnosed which he did in February with vascular dementia, since then he has become bed bound has carer's 4 times an day apart from that he has us phoning or visiting when we can. He has become hard to manage at times as I'm writing this I've had 43 miss calls plus others where I've answered, I know he will be extremely lonely we have ask for bereavement support ect but everyone says he is Ok till he bothers them, I.e carers he previously had moaned as he was making serveral nuisance phone calls in the night so our suggestion of taking number out the phone was quickly stopped incase he needed the carer's even though we said he doesn't seem to know what an emergency is and he would ring us and we would ring an ambulance especially as we wouldn’t ring carers they have enough to do, but even though they didn't want number taken out of the phone they would ring us expecting us to go over to sort him even though an all round trip is just over an hr, even though we had refused this didn't prevent them phoning again other nights but then he ended up on hospital so they was no longer in charge of care. Now we are not having the best of times, I know most of it is down to loneliness and he gets attention from his actions he won't move closer, neither go in residential care but no-one will offer any support to help us combat this or helps us communicate in away that doesn't upset him. We both would love if we could look after him 24/7 but been realistic we wouldn't cope as we struggle to look after ourselves at times but also i work part time and my partner is in full time work after working his butt off for over 5 years voluntary and part time due to his needs he requires extra support which may come across an little selfish but we are 32 and 34 which means we aren't entitled to any money at first if we leave our jobs and likely hood of us getting jobs easily again is very low. If anyone has any suggestions of things we can try to settle him as we want him to stay at home for as long as he wants but to be happy and settle we know some days will be hard but there's no break at the minute and definitely no real support many thanks all
MB
saysMy mom is 71. She’s lived with us for almost 3 years. I eventually was up most nights as she would wander and I was afraid she’d fall down the stairs as she would forget where she was and go into different rooms in the middle of the night. She was often confused and required assistance for meals, showers, meds, finances. It broke my heart to put her in a home in May. I love her so much but her safety especially with my going back to work was at risk. She begs regularly to come home. I decorated her room and she took it all down. She has been there over a month and will not sleep in the bed. She cries when I go there and asks me where she is, what the address is, why I put her there and how can I sleep at night knowing what I’ve done to her.. When I take her out she is happy (but regularly confused) and when I bring her back and leave she seems worse. She is so angry if I don’t take her for a drive and yet is so upset after I do. I cry often and feel so guilty. I know she needs the care. The place is wonderful but I wish I could have kept her here. Trying to soothe her while she is so angry and upset while also trying to deal with missing her tremendously makes me feel so sad. It’s such a hard thing.
Lynn
saysMy Mum went into a home 2 weeks ago for the exact same reasons. Before she went in the benefits and safety issues outweighed my feelings of how I much I would miss her.. The care staff say she is content but I've seen her 3 times and she is always anxious and asking to come home. My guilt is overwhelming and keeps me awake, I cry all the time. I hope she settles, everyone keeps saying she will but I wish more than anything she hadn't left..
I hope you feel better soon, and I hope your Mum settles eventually.. The only thing that keeps me going is that she's safe.
Janis Godwin
saysI feel bad for you we just placed her yesterday and all I do is cry, cannot imagine going to visit her as she was angry when we left her
John
saysI’m so sorry to read these stories. My Mummof just 89 was recently put into a care home by her LPA, my elder sibling sister who we don’t get along with. I came home from shopping the other day and my Mum had been kidnapped (that’s how it felt) they took my Mum away behind our backs without consulting us (myself and my other sister) we are absolutely distraught. I had been living back at my Mum’s house for the last couple of years and this is the hardest days of my life. My Mum is now a 3 hour drive from me. Naturally she’s very confused and keeps begging me to come and take her home when I call her. It’s absolutely heartbreaking! So sorry to read all the other stories of loved ones who’s parents are suffering with this awful disease. 🙏
We're really sorry to hear about this situation with your mum, John. It sounds like this is a really difficult time for you and your family.
It sounds like you might benefit from joining our online community, Talking Point, where you can talk to others affected by dementia, and get advice from people who have been in similar situations: https://www.alzheimers.org.uk/get-support/dementia-talking-point-our-on…
Also, please know that if you or your sister ever need more support, then you can always call our Dementia Connect support line on 0333 150 3456 for information and advice. More details about the support line (including opening hours) are available here: https://www.alzheimers.org.uk/dementia-connect-support-line
We hope this is helpful.
Alzheimer's Society blog team
MB
saysThank you Lynn, I really appreciate it. Hopefully they will both settle and we will cry less. It’s such a hard thing that pulls at your heart. I try to remember that when I feel so awful. It’s a painfully difficult thing and it’s ok to feel awful about it. ...and eventually, hopefully with time it will feel less awful for all involved. Sending love to you and your Mum.
Janis Godwin
saysI feel for you, we put my mom in a home , shes 93 with dementia, had hallucinations called 911 all the time, has fallen many times refused health aides, so had no recourse. Its only been 2 weeks still angry and upset cries when we see her and when we leave, horrible....
S l smith
saysI know exactly how you feel I am going through the same dad has now been in a home for or 4 months and I am still carrying the Guilt I go see him nearly every day, and I take mum with me three times a week, and all he does is blame mum and accuses her of all thought which is very distressing for Mum and me, dad's mobility is not very good so he is in the safest place that still does not make me feel any better as he always asked when he is going back to his own house and all I can say to him is when you get better which is I know a compassionate lie but seams to settle him , but I hate myself for lying to him and I am trying to live with this everyday day and every day I cry,
We're so sorry to hear about the difficult time you're going through.
Please know you can call our Dementia Connect support line on 0333 150 3456. One of our trained dementia advisers will listen to your situation, and offer specific information, advice and support. More details about the support line (including opening hours) are available here: https://www.alzheimers.org.uk/dementia-connect-support-line
You might also like to join our online community, Talking Point, where carers and other people affected by dementia can share their experiences and support each other. You may find there are other people who have been in similar situations who can offer their own personal advice. You can browse the online community, or sign up for free here: https://forum.alzheimers.org.uk/
We hope this is helpful. Please do call our support line if you need us.
Alzheimer's Society blog team
Annie
saysMy 99 year old mother is in residential dementia care transferring from hospital for assessment. She doesn’t have capacity but has for the whole time been fixating on going home wanting live-in care. This is unlikely to work as she would be confused and not like or accept someone else in her house. She couldn’t be left overnight. Taking photos/memory items to her doesn’t work and any little treats are seen as trying to get round her. She is unhappy that I can make decisions but doesn’t understand the need for it.l am seen as despicable and the baddie in the situation. Visits result in her ranting and both of us distressed. Coping with elderly relatives as we ourselves get older is difficult. I empathise with some of the problems others are going through
C.M. Cordero
saysMy father has had a severe stroke, which left him unable to use one side of his body. He is incontinent,in a wheelchair, and must be taken out of bed on a hoist. He is also in the middle stages of dementia and is having delusions.. He has been in a skilled nursing facility for a year. He wants to stop my sister's power of attorney and sign himself out to go home. He has friends who say they will care for him . They are not trained caregivers. At least one is expecting quite a bit of money to care for him. Also, his house is not set up for someone as disabled as he is. Still, he might be legally able to do this if he is not declared incompetent. If he goes home, we fear harm will come to him. He will be back in an ambulance again shortly.
Debora
saysEither you or your sister need to apply to the probate court for an involuntary conservatorship of his person and his finances. They are two separate things. If you guys dont want the responsibility the court will appoint a conservator and will get paid by the estate.
C.M. Cordero
saysThanks! My brother is going to do that.
Karen A Bolles
saysMy sister feels she has "abandoned" her husband by putting him in a memory care facility. She goes for a visit and he begs her to stay there with him when she tries to go. What can we do for her? Her health has declined again, like it was as a 24/7 caregiver.
Hi Karen,
Thanks for your comment, and sorry to hear that your sister's health is declining again.
We have some information on our website that you might find helpful. There are some useful resources on this page, which is specifically around managing emotions and accessing support after a person has moved into care: https://www.alzheimers.org.uk/get-support/help-dementia-care/care-homes…
If you or your sister would like more information and support, then you may also find it helpful to talk with one of our dementia advisers. To speak to an adviser, just call our Dementia Connect support line on 0333 150 3456. You can find more details about the support line here https://www.alzheimers.org.uk/dementia-connect-support-line
Really hope this helps, Karen. And please do call the support line for more information and support if that sounds helpful.
Take care,
Alzheimer's Society blog team
Yvette Lambert
saysDon’t think I will go to my grave beating myself up about putting my husband into a carehome but the carers coming in confirmed it was dangerous for him to stay at home with all his constant falls. He had vascular dementia, epilepsy and COPD. He was in carehome four months and then in hospital with infections where he passed away after five weeks. My guilt is not bringing him home to pass away. Lockdown was a nightmare only seeing him at end of life..The guilt I feel is awful.
Yvette, we are so sorry to learn about your recent loss.
Our dementia advisers are here for you on 0333 150 3456. They're available seven days a week: https://www.alzheimers.org.uk/dementia-connect-support-line
You may also find it helps to talk with others who may have gone through or are going through similar experiences. If you think this would help, you can visit our online community, Talking Point, for peer support: https://forum.alzheimers.org.uk/ It's free and open day or night.
Cruse Bereavement Care also offer support, advice and information when someone dies: https://www.cruse.org.uk/
Please do call our support line if you need someone to talk to during this difficult time. You are not alone.
Alzheimer's Society blog team
Pamela. Hodson
saysHusband in care home for respite. Now social services say he can't come home.surely as it was only tempory I can bring him home. Thinking of seeing a solicitor.
Hi Pamela,
We're really sorry to hear about this situation with your husband.
There's some information in this blog article which you may find helpful: https://www.alzheimers.org.uk/blog/moving-out-care-home-during-coronavi…
Each case can be different, so if this does not help please do call our Dementia Connect support line on 0333 150 3456. One of our dementia advisers can give information, advice and support. https://www.alzheimers.org.uk/dementia-connect-support-line
Hope this helps, Pamela.
Alzheimer's Society blog team
Keith
saysMy mum want to go home to where her brothers are. (Sadly they died years ago).
I used to drive my mum round for 20 minutes till she forgot.
Now my car's broke down I use another tactic.
I say they are decorating and that she can go back tomorrow when they've cleared up and the paints dried.
If worse comes to worse I ring my brother and he pretends to be the one decorating and he says what a mess the place is in etc.
Just the thought that she will be going home at some point settles her.
Tanya Seeley
saysKeith what a wonderful way of doing something meaningful with your mum. Sorry to hear your car broke down. I am glad to hear you've found a plan B. We teach this all the time, "to live in their reality".
Annia Leonard
saysMy mother in law came to live with us almost a year ago. She has started telling us she wants to go home but when we take her to her house she argues that this is not her house or her things and demands we take her to her home! But she has no idea how to get there. She has been diagnosed as having dementia. She gets very angry at her son and I don’t know how to handle it.
Karen
saysMy mom has been in a nursing home for almost 9 months now. Recently I decided to talk to a therapist because the guilt was hard to deal with and the phone calls with her are never good. Tonight for example she left a voicemail telling me that I must have the devil in my head and she doesn’t know what happened to me that I would put her in such a place. It was a long voicemail with plenty of insults. I am the only daughter with one brother who is 12 years older then me and he is having a lot of medical issues and my other brother passed away in 2005. The therapist has helped me but it is still so very hard to listen to her voicemails or talk on the phone with her. Our 20 minute visits once a week are usually fine and we can talk about my grandkids or other family members. She will always bring up that she doesn’t want to be there and gets upset when our 20 minutes is over.
I wish there was some type of comfort I could give to others going thru the same thing with their parents t but all I have to really say is that you are not alone and try to be easy on yourself.
Connie McKeen
saysMy mother has dementia and just went into a nursing home a few weeks ago. She is very upset with us "kids" as she wants to go home. She says she misses her place and being able to cook for herself. And said she misses feeling useful as there is nothing to do in the nursing home. She was crying yesterday..( I have never seen her cry) saying that we are awfully for dumping her in there, without giving her a choice. She is still very sharp...so its difficult to change subjects. Because she knows what your doing. And explaining anything only upsets her...and she has a reasonably argument for everything we say. I feel horrible that she is in there. And I would take her if I could. But I cant at this time. She said she feels herself getting more and more unhappy. (She is usually a happy person) And that we might as well have shot her with a silver bullet. Because she does not want to live there her whole rest of her life. The staff have said that she is telling them also that she wants to go home. We thought it would be better after her 2 week quarantine. But it's not gotten better. The recreation department said she has very much enjoyed the recreations. But she tells us she does nothing in there. I'm not sure if its because she does not remember or that she does not want to admit she likes something about the place. Because of Covid we are not able to even visit outside. Today she threatened to walk home. Is there some way to make her happy? Or understand that we were not being terable kids who abandoned her there? If you talk to her it's hard to catch her dementia, unless you asked certain questions...like what happened yesterday or who she talked to yesterday.
Can you please give me and my siblings some insite.
jan
saysi’m in the same boat but my husband of 50 years. it’s hell watching them!
Connie McKeen
saysI wish you the very best with your husband. I hope that his and your new life will be as happy as it can be.
Judith
saysHello, this is my first visit to this website, you have just described my mother and our situation. I don’t have any suggestions but just wanted to say thank you for your question.
Connie McKeen
saysThank you for your reply.
My mom surprised us by saying that she has finally excepted that she will be living there. After she called the police twice saying my sister was keeping her keys and wallet we thought she would never except it. But I think with the fantastic staff and love and support from family, She realized we were all trying to do the best for her.
I found at first I was trying to placate her by saying maybe on a few months when I moved she could live with me. I think it helped for a few days...but ultimately it just confused her and slowed down the acceptance. I think they go through the same steps as a person who lost a loved one. Disbelief..confusion...denial
..sadness ..bargaining..anger..and then acceptance.
She is now looking forward to getting her own room eventually. And is starting to nest. Asking for face cream.. her clothing, jewelry and a few of her favorite things.
I'm now hoping she will make friends and that covid restrictions will be lifted soon.
I wish you and your family many blessings..I hope all goes well.
Peter Rodgers
saysThe rules covering dementia and care in general are inhuman to the sufferer snd loved ones especially when the dementia is in the early stages. My wife has dementia following a subarachnoid brain haemorrhage. I wish to move to Sheffield taking my with me (to a care home). But the obstacles are horrendous.asshe is in the early stages she needs family support
Ruth
saysThis is my first time on this website. I just got out of work and my mother-in-law called. She tried calling my husband and when he was unavialable she called me and said she wants to go home. I don't how to deal with it. She's in such a lovely facility with all her familiar furniture and photos, books, nick nacks, but it isn't home. Thought I'd check online for what and what not to say before I called her.
Hi there Ruth, thanks for leaving a comment.
It sounds like you might benefit from talking with other people affected by dementia within our online community, Talking Point. Feel free to browse and read others' experiences, or you can create an account to reply and connect with others. You may find similar situations to your mother-in-law's shared there: https://forum.alzheimers.org.uk/
You can also speak with one of our dementia advisers by calling the Dementia Connect support line on 0333 150 3456. They will be able to provide you with dementia information and advice. (More information about the support line, including opening times, here: https://www.alzheimers.org.uk/dementia-connect-support-line)
In case it helps, here's another article we've shared about what not to say to somebody with dementia: https://www.alzheimers.org.uk/blog/language-dementia-what-not-to-say
We hope this is useful, Ruth.
Alzheimer's Society blog team
Thembisile
saysMy grandmother she doesn't remember Anything she is talking to her self . She is 86 years. She has an anger when you try to talk to her I think it started 4 year ago I do really think what should I do please help 😭😭😭😭
I am 15 years old
Hi Thembisile,
Thanks for getting in touch, and sorry to hear about this situation with your grandmother.
If your grandmother doesn't already have a diagnosis of dementia, then encouraging her to see a GP would be a good idea. You may find this page on our website helpful:
https://www.alzheimers.org.uk/about-dementia/symptoms-and-diagnosis/how…
Once a person has a diagnosis, they will be able to access a wider range of support.
You may also find it helpful to talk to one of our Dementia Advisers, who can learn more about your grandmother's situation and provide relevant information, advice and support. To do this, just call our Dementia Connect support line on 0333 150 3456. You can find more details and opening hours here: https://www.alzheimers.org.uk/dementia-connect-support-line
Hope this is helpful, Thembisile. Please do call our support line as they'll be able to give more specific advice for you.
Thanks,
Alzheimer's Society blog team
D.S.
saysYou obviously care a lot about your grandma. This is a hard situation. I'm 37, and I'm having trouble with it! The best thing I did was educate myself about what it means to have dementia. It's important to understand that the things your grandma is saying and doing are not truly what she wants to say or do. She has a disease that is affecting her brain. Treasure the memories you have of her before dementia. Know that those memories are who she really is, and now this disease is changing her brain. It is very sad. Whenever you can, tell her you love her. Ask your parents about what kind of dementia she has and learn more about it. I'm sure your parents are under a lot of stress too. This is such a difficult situation and you seem like a wonderful grandchild.
Connie McKeen
saysI'm so sorry you're going threw this with your grandma. Just remember what is happening to her is part of the disease. And so is the Anger...but it will eventually subside.
Just remember no matter what happens, she is your grandmother and all she needs from you is love, because she will never stop loving you.
Please take care.xx
Wendy
saysMy mum fell and broke her arm on 10th March. The orthopaedic doctor did not want to admit her as they were not going to operate just put her in collar and cuff. She was admitted anyway?? For 2 weeks we were unable to see her so phoned every day to see how she was. She was confused on days and it wasn’t until the second week she had been in that we were allowed to speak to her on the phone. Then we got a call to say we could go up as she was critical. She had caught pneumonia in hospital and I stayed with her through the night on Thursday 25th and Friday 26th then she passed away Saturday morning. We are so angry and hurt we could not see her for the 2 weeks and have now found out the hospital guidance is that a patient who has dementia and confusion should be allowed a visitor.
She went in with a broken arm and is now dead it was horrific what we saw and I feel so guilty for letting them admit her and not knowing how she was over those 2 weeks without us there.
Wendy, we are so sorry to learn about your recent loss.
Our dementia advisers are here for you on 0333 150 3456. They're available seven days a week: https://www.alzheimers.org.uk/dementia-connect-support-line
You may also find it helps to talk with others who may have gone through or are going through similar experiences. If you think this would help, you can visit our online community, Talking Point, for peer support: https://forum.alzheimers.org.uk/ It's free and open day or night.
Cruse Bereavement Care also offer support, advice and information when someone dies: https://www.cruse.org.uk/
Do call our support line if you need someone to talk to during this difficult time.
Alzheimer's Society blog team
Angie
saysMy godmother has 24 hour live in care at her own home with 2 main carers who do 2 week shifts (me being one of the carers), she is 91 and had an aneurism a few years ago but is like someone with fully blown dementia. She is also always wanting to go home despite being at home and not in a care home. There is no quick fix solution when she gets into going home mode or quite often going to the doctor. Photos, music, feeling safe etc do not work but diversion is the only answer and even after that it can take a couple of hours and post a day sleep/rest when she will have forgotten. You need to ride the wave with her which is stressful and difficult. Telling her she is in a safe place etc makes her furious. Having read all these stories, each case is v different. The outbursts of wanting to go somewhere need to be humoured with very good excuses as to why they can’t get there and I often get one of the family to ring and tell her something v comforting as to why she can’t go home etc as the only solution in my opinion is diversion. Easier said than done. I often put something she loves on you tube. Ballet in her case and sit with her with laptop on her lap. She gets engrossed. Then leave the room (in my case that is possible), as she will still associate me with the going home etc and need to break the pattern in her head. It’s not an immediate fix but over a couple of hours will work.