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She has had several falls at home, they scared her, and she decided (with our "help") that assisted living was good. After the falls, came 3 weeks of rehab and we finally moved her to her new "home" yesterday. She has dementia and was very confused, overwhelmed and like a deer in headlights. At the end of a very busy day (along w/ a party for the ASL facility for an award won), she wanted her car, her money and to go home! She feels like my sis and I just "left her" there, stranded. We have to work full time, but will see her later today. It is heartbreaking to see. Mom totally forgets that she was actually "excited" about moving here just 3 short weeks ago! Any words of wisdom for her 2 heartbroken daughters?

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It is heartbreaking and her being in AL is necessary.

You expect her to want out; this is a given. Study / educate yourself on what dementia is and how to communicate with a person inflicted with it. The brain has changed / cells are dying and continuing to die. Her behavior will continue to change:

Fearful
Defensive
Confused
Angry
Want to go home
Not trusting (you / family / staff)

Talk to a medical social worker.
Once you understand she will re-act this way and perhaps be more insistent (I want to go home), it is important to know how to manage:

1) Redirect.
- Never argue. Say I understand you feel xxx
You gauge how you respond according to how severe the dementia is.
- Change the subject.
- Give her hope "Yes, we are working on getting you home..."

With dementia, of course she felt excited three weeks ago and doesn't now. This is what dementia is.

Supporting her daughters:
- Listen. They need to get their feelings out. Emotionally it is heart wrenching.
- Educate. on what dementia is to understand how to proceed (google Teepa Snow) / Watch her webinars or You Tubes.

To the person inflicted: You give HOPE and stay COMPASSIONATE.

- You learn what and how to give non-verbal cues, i.e.
--- smile
--- tone of voice (soft)
--- make eye contact
--- gentle touches as they are receptive

Get this book:

The 36-Hour Day - 7th ed. - A Family guide to caring for people who have alz disease and other dementias by Nancy L. Mace, MA, and Pater V. Rabins, MD, MPH.

Read this article: 

8 Types of Dementia and How to Recognize Their Symptoms, According to Experts-Because Alzheimer’s disease isn’t the only one to have on your radar

As the daughters may need, hire a medical social worker to support and help manage this new situation / transition. Make sure all legal matters are in order.

Give the mother a hug and tell her you love her. Gena
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Reply to TouchMatters
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Of course she hates it wouldn’t you? You’re taken out of your home and put in a sterile place with people you don’t know. You’re forced to do things on their timetable you eat you shit you do their exercise. essentially it’s a jail for old people. They also know it’s where old people go to die and it just reminds them their turn is next
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Reply to Sample
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This isn's just about AL. Everyone is stressed with every move, at any age. It is just harder for Mom to process. New place, new people, new routine, new everything is hard for an old brain. Whatever you do, don't blame yourselves or overthink this. This is good, this is right, and it isn't just about what Mom wants; it's about what is best for everyone.
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Reply to DrBenshir
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My late Mom always said "you live long enough you will end up in a nursing home" She ended up there as did my Dad. She had to go Dad just had the money to go in with her needing some assistance. She fought it every day of her life. Dad just decided to fit in. He was sound of mind,Mom had dementia. It was sad for her but it was the only solution. What I find every egregious with these places is putting folks in rooms with strangers. my folks had money to have a room to themselves and when Mom died Dad had a private room. But very, very few of us have that option. Elder care is sinfully expensive. Many facilities are not good places to be. The one my husband was in was horrible. Thankfully he was only there for 2 weeks for rehab. Rehab was great but the rest was just horrible. Dirty,smelly, very understaffed. Residents screaming, going to the bathroom in the halls and not being cleaned up quickly. I never heard so many "Not my job' excuses in my life. I,among others, complained loud and long, still warn people to go anywhere else but there, yet the place is still open. When it first opened it was like a resort. Privately owned, actually reasonably priced, beautifully furnished, well staffed. Then the owners died, the "kids" wanted nothing to do with it and it went corporate. Tragic.
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ElizabethAR37 Nov 25, 2025
"Going corporate" seems to be a death knell for previously reasonably well-run healthcare facilities. When care for vulnerable people is sacrificed to profit, what should we expect? Only in America is healthcare blatantly regarded as a "profit center".
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My grandpa started off in an ALF as he became too much for my family to handle as we also work full time. He was falling, wandering, leaving stove on, leaving water on, making threats to himself and my family, calling cops with wild claims, threatening neighbors, but eventually the ALF said he was too much for them to manage and suggested memory care. After a hospitalization and some testing he was diagnosed with moderate vascular dementia and depressive mood disorder. (Add that to his PTSD and anger issues and you get a plethora of reasons)
Needless to say he HATES his MC facility and voices it to anyone who will listen. Our visits revolve around me needing to get him out, why havent I gotten him out, its my fault etc. I have reminded him that he hated living alone, he hated living with us, he hated the ALF and now he hates the MC. When I visit I never know if I am going to get a small moment with the OLD grandpa I remember OR this angry person who has tormented me and my family for the last 5 years. I am the only one left in the family who still speaks to him (ALL other members quit years before he was diagnosed) and I am his POA so I feel an obligation to continue to try. He has put me through the worst times of my life and still tries when he can. Anytime he meets a new person he tells them I am forcing him to live there even though he is FINE, and that he needs to call a lawyer to sue me. He gets hospitalized for something and tells every doctor that he is being forced to live outside of his home and that I am stealing from him. (using HIS money to pay for HIS facility is stealing in his mind since he does not want to be there) Then when he tells me he wants to go home I tell him that all the accusations he has made and terrible things he has said have made it impossible to come home with me, then he claims he never said any of that stuff and everyone is lying to me. ( I have documents from APS where he claimed all this not once, not twice but three times)
I am in therapy and see him MAYBE twice a month. Generally one of those visits is terrible and I have to walk out. My anxiety is SKY HIGH everytime I even think about visiting. I feel for you that you have so much love for your mom and want her to be happy.
I have found this forum to be very helpful and I think all the answers are pretty much agreeing that she needs some time to acclimate. Sometimes they do and sometimes they dont. There are residents at my grandpas facility who are happy and smiling and friendly but then there is him who is always scowling and complaining.
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mm61972 Nov 23, 2025
I related to this so much with my father. He has punished me for being the only one still around to help him. Accusations of theft, abuse, everything - just because I make clear I can’t do it all on my own. It’s such a hateful relationship at this point, and so bad for my mental health.
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It is easier to think of it as that you are dealing with the dementia not with your mum. It is ok to lie to dementia. Tell her it is just for a little while and then if she doesn't like it she can leave (maybe her house is being renovated) , in that time she will hopefully start to adjust, if not just keep up with the , little while longer excuse in the meantime talk up the place , chat with resident s with you mum, do all the things you would do to help your child adjust to a going to school. Be positive, act like it isn't my as big deal, don't get the upset. Tell her whatever you need to that you think would help her feel less stressed.
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Reply to FarFarAway
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my mother did this. we basically ignored her requests to go home [ since she sold her house ] or put her off [ we’ll discuss that later, let’s enjoy out dinner now]

her dementia has increased to the point that she would not survive a day out on her own, but luckily she doesn’t seem to remember living by herself.

ironically her disease will make this easier on her and on you two, in time, meanwhile, either redirect, ignore, or ask the staff what they recommend. that’s what they’re there for.
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Reply to eridanis
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I’m in the same situation as you. I believe any adult child who is responsible for their parent experiences this. I don’t think there is a good answer. I did read through the responses and agree with most.
It is heartbreaking to watch your parent go through these changes.
I think some people think they find the “perfect place” at the beginning. In my opinion there is no perfect place. We have just moved my mother for the third time in a year. We did make a mistake putting her in AL instead of MC. If your parent has dementia, it will only get worse so might as well start with MC to avoid moving.
Originally I would go visit almost all day everyday, then again at bedtime to help acclimate her. I’m not so sure that’s the best way. I think it caused her to be too dependent on me being there.
She moved to a MC yesterday and we only visited her for about two hours today. We will try this and see if it works better. I do NOT agree with not seeing them at all for two weeks. They are fragile and need to not feel they’ve been abandoned. 🙏
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Reply to klhsho
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I felt no guilt for moving my mom into assisted living, as it simply had to be done, which is exactly what has happened for your mom. What I did feel was sadness for her situation, for her confusion, for her continuing loss of all that had been hers, including her memory. I knew the place where I moved her very well. I visited her and got to know the other residents and staff. I took her out for rides and walks, her hairdresser, and even dinners once in a while, never anywhere near her house she had to leave. It turned out she was for the most part happier there at assisted living. She had fewer worries, replaced by activities to keep her occupied. Many times over the years she got confused and wanted to go "home", wherever that was to her at that point, but she could be talked out of it or taken for a ride and forget about "home". Just be there for her, comfort her, let her know you understand her feelings, redirect her, and say ........ (whatever you come up with to calm her).

Another lady had moved in on the same day as my mom and that lady was more than a "deer in the headlights", as you say. She wasn't at all quiet about her anger at the situation. Funny thing though, this lady took a liking to my mom, while everyone else in the facility she saw as terrible, stupid, mean, or criminal. One day during the first week she and my mom were caught walking away from the facility adorably holding hands. When the director caught up with them, one house away, the lady said they were going for a glass of wine and a movie. The director told them they forgot their wallets and led them back. The lady eventually had to be moved out, as she was way too much trouble. But my mom stayed and everyone there loved her.

There will be so many stories to remember and tell about this stage of your mom's life. Some funny, some sad. Buckle up and enjoy whatever you can on the ride.
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Reply to ArtistDaughter
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There are just no easy answers. Whatever you do, it won't be a perfect solution. That's how I felt. I hated that my mom didn't want to be at her memory care center (which, by the way, was excellent and they took extremely good care of her). It broke my heart that she wasn't in her own home, but it wasn't possible for many, many reasons. My mom was fine for about three weeks and then wanted to go home. Every time she saw me, she complained bitterly. When she'd start complaining, I'd divert her attention. I couldn't reason with her -- you can't reason with someone with dementia. I'm sorry -- but you'll have to accept that she'll probably never really like it and always ask to come home. But it's not possible. That's the safest place for her. Just remember that his sucks for everyone, but you're caring for her as best as you can. There are no perfect answers in any of this.
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Reply to Jacquelinezr
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Wendy25: Prayers forthcoming.
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Reply to Llamalover47
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After my late mother suffered several falls at home in our CA place, it was time for rehab and assisted living placement. She hated it and always asked me to take her home because her lack of judgement made her forget that she suffered fall injuries. My brother moved her to OR where Mom got better care and able to adjust to new living.
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Reply to Patathome01
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There is no way around it. She has to settle in and get used to it. She shouldn't have her car or her money, and she can't go home. At home care will be more expensive the assisted living if she requires several hours of care each day. You are doing the only thing you can do, and she has to stay. My Mom (no dementia, but several falls and broken pelvis) wanted to leave the next day. She asked why we would put her in a place like that where people were in and out of her room everyday. About 4 years later, she has decided she'd like to move to a different place. Not happening - I am at my limits for dealing with this.
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Reply to Lylii1
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When I first got my mom to Al, she forgot why she was there and she wanted to be with people! Initially she wouldn’t go to Dining Room and “ eat with those old people”. So they brought meals to her, we all stayed away except for very short 15 minute check-ins and let her know we cared, but let the staff work with her to get her acclimated. It took time, but in a few weeks she had new friends, was at Bingo, etc and eventually agreed that her new living arrangement was like living in a Country Club! It gets better—though those first two months were hell! Once they got her settled and understood her moods, they gave her Serequol to minimize sundowning.
good luck! Let the caregivers lead, you have to let her acclimate! It’s like a toddler and the first day of daycare!
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Reply to PaulettePT
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This is normal. We ended up putting my mom on an anti-depressant. She really needed it years earlier. I would say that it took a couple of months for my mom to settle in. She's good now, but she does have Vascular Dementia and forgets why she's there and how long she's been there.
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Reply to darts1975
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It gets better, but it takes time. My mom complained bitterly for months. Later, at one point during a visit my mom asked me to leave so she could go to an event her MC was having.
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Reply to JustAnon
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First, it will take a few weeks for her to adjust.

Second, often people in senior facilities will do very well on their own but as soon as a family member appears they become full of woe and beg to leave. They are kind of like a child who cries every day about going to school but when you peek at them in their classroom they are engaged and fine.

Third, if she continues to be overwhelmed, you may find memory care a better fit.

But she will settle in. Just give it time, for all of you. Keep us posted on how it's going.
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Reply to MG8522
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Ok, I am of the belief that a person with dementia should not be in AL but in Memory Care.
If it is possible to get her into MC and out of AL I think that would be better for her.
MC is going to be smaller, not as much going on so there will be less confusion.
I think a busy day then a party for the facility that she right now has very little connection with was a bit much.

No matter where she is she will want to go home.
She will not be "happy" to be left there by the people that she relies on and trusts. She is going to have to learn to rely and trust the staff. that can take some time so you need to be patient.
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Reply to Grandma1954
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SKaauwai Nov 18, 2025
Agree! My father was in AL but they are not equipped to deal with advanced dementia patients. Our AL has two nurses for the whole place, and they don't work on weekends. The others are mostly just medtechs or aides who are not really well versed in dementia care.

Memory care is probably the best place if you can afford it!
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I had the same experience. Mom (91, dementia, wheel chair) agreed to the ALF move but freaked out when we got her to her new apartment. She yelled, screamed and threatened all sorts of things, wouldn’t wear the pendant they gave her - it was a really terrible experience for her and for me. I stayed with her 2 nights and one full day. Each time she started screaming I left her room (to cry) and she was calm when I returned. Then I left her alone for a weekend (for my sanity) and began visiting her just 2 times a week and calling 2 times week.

I talked to the staff to find out how she was adjusting and get to know them. A few residents were very kind to me too. Assuring me she was doing fine. I worried she’d never be able to find her apartment, the dining room or check her mailbox. But when I backed off the staff did their job and took care of her, helped her get adjusted and they assured me she was doing fine. The place your mom is at won an award for something - so I think that is positive.

I got used to telling her I had to go home even though she would whine. I hated that but I went stealth and tuned it out knowing she’s being well taken care of when I’m not there.

I experienced remorse, grief, and often pondered moving her into my home. But knew I just had to stick with it and with time we would both adjust.

Reading posts and responses on this forum helps me keep things in perspective and shortens any bouts of sadness and grief I have. This is a universal experience and so many have wisdom to share.

Today, just over a year later, she’s content and has accepted where she is in life. She knows where everything is and checks her mailbox on her own. She looks better than she has in years, wears earrings, changes her
clothes more often, and eats better food than she did at home on her own.

I still see her twice a week and I’ve spent a few nights when she was sick or had a fall. She knows I’m close by and love her but that I’m not giving my life over to her and she never wanted that.

Hang in there and just visit every few days. It will help her adjust and give you a healthy break. You will both have good days and bad days (or weeks), but stick to the plan and give the plan a chance to work.
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Reply to FanBlast
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Daughter62sad Nov 18, 2025
Best answer ever!
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If her dementia is too advanced, she may actually need memory care. Keep close communication with the AL staff during the next few months. She may just need more time to make some friends, start trying the activities, etc.

My mom was not thrilled about AL after moving from IL after a fall and rehab. But she admitted the food was better. She complained about not being able to play as much bridge, but now she has picked up other games including mahjong. She has new friends, including a new boyfriend of sorts. The new place has 2 happy hours a week, and now with the assistance, she goes on the weekly outings and shopping trips that she mostly missed in IL. Long story short, it's been a year and she is now very content and her cognition actually seems to have improved. The stress of being more independent was clearly taking a toll.
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Reply to ShirleyDot
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Give her weeks, maybe months, to adjust. It's clear that she can't live at home anymore. BUT. She's not going to understand that because she has dementia. So, as much as you'd like to keep explaining why this is better and she'll be safer and whatever other arguments you come up with, do not argue. The appropriate thing to do is to distract, distract, distract. Keep changing the subject. Keep her busy with activities when you're with her. Encourage interaction with the staff and her new friends.

"Mom totally forgets that she was actually "excited" about moving here just 3 short weeks ago!" Yup, and she will forget what you say to her about it today and forget why she went there (no matter how much you remind her) and she will keep forgetting, wherever she is. It's a sad truth but in a way, it's comforting because forgetting means that she forgets the sad things she's thinking about today.

When dementia walks in the door, happy flies out. Keep that in mind, and don't keep breaking your hearts over and over time and again. Accept that this is how she is now and that she is exactly where she needs to be. Eventually, if you let her be, things will even out and she'll only know her here and now in the facility.

Best of luck on this difficult journey.
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Reply to Fawnby
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MomsBrain Nov 14, 2025
Good wisdom here, though hard to hear. 😥
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Hire a temporary CNA for a few weeks or so to be your mom's helper. Every day for a few hours...maybe in the afternoon starting with lunch. She can help your mom acclimate, make sure she's eating, socializing at least a little bit. She has dementia and likely will not retain a lot of your pep talks from before. Ask the facility to cooperate with CNA....(Sometimes the other CNAs don't like working with a private aide). Your mom needs a little help and someone to help her around. I did private care all the time, especially when family members couldn't or wouldn't help.
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Reply to Hrmgrandcna
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Didn't they mention not visiting for 2 weeks so she gets used to the new situation?
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Reply to lkdrymom
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Of course it is a big change.
Remind her of the perks...no more cooking, cleaning and laundry! Mention this every visit, how "lucky she is."
You may need to stay away the first few weeks, see what they say.

Don't feel guilty, you are doing exactly the right thing to keep your Mom safe. Nobody likes getting old and having these problems.
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ElizabethAR37 Nov 18, 2025
I so hope that when/if I need to be "placed", I will be able to recognize the positive aspects like no more cooking, cleaning, and laundry as well as the less positive. As I struggled to load heavy grocery bags into my car today, the thought crossed my mind that maybe an ALF might not be the worst thing that could happen to me (age 88) and my husband (96).

However, there's a significant financial aspect to consider as well. If we live more than a few years longer, we might outlive our resources and need Medicaid--if it's still available. That could mean a much less desirable facility. We do NOT expect our family to use any of their funds to support us. I wonder how many of my fellow old-oldies are concerned about this issue.
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This is very typical, sad to say. In fact, some places will tell you not to visit for a while, so the new resident has a chance to fit in on their own, but I know that would break your heart further and be very difficult to do. I agree with the comment above who said just sit with her in her pain and sadness. I feel I did not do very well with this with my mother, and it made her even angrier when I pointed out all the good things about the new home. HUGS.
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Reply to MomsBrain
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Of course she wants out.
Doesn't everyone?
As my brother said to me: "Hon, it's like when I was younger and in the Army. I don't much like it but I make the best out of it".

Let your mother be unhappy about this. Isn't that normal? She has sustained another awful loss, her home. Wouldn't you grieve that? Let her say how sad she is, listen, and tell her you are so sorry, that you realize this is a huge loss, that you hope with time she will adjust to make use of some of the finer things about this.

If not? She's had a long life. There were many times it was less than perfect. And she had to sit and understand that she had love, a roof over her head, and that was more than so many.

Here is the KEY to this. You and Sis need to get to your core that
YOU didn't cause this.
YOU can't fix this
THIS is sad, but the right word is grief, not guilt.
AND you cannot be responsible for the happiness of everyone.
Life isn't about happiness, and especially the end of life isn't; at 83 I can ASSURE you of that.
Cling together, but stop looking for answers where there are none. You can't afford to expend that kind of energy.
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Reply to AlvaDeer
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You are wonderful daughters! Please give it time. She is safe.
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Reply to Caregiveronce
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You did what was best for her, but you also cannot blame her for feeling the way she does. I don't think I have ever ran into someone that rather be in AL then their own home.

Don't beat yourself up, it is normal to long for what was.
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