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My husband and I are homebodies. He pointed out to me recently how much we would have LOVED quarantine alone. Watching movies, playing on the computer, going for walks, just relaxing in peace at home. Frankly, we were living the quarantine life before the pandemic hit. But now that my father lives with us I feel like he's on a permanent vacation and my husband and I are his staff. I have to constantly make sure he's constantly busy doing something otherwise he's nodding off on the couch midday, chewing the crap out of his fingers (which I had to bandage one last night) or sitting there just staring at the wall. He will not show initiative and do something on his own. I put a movie on for him and I can't get him to tell me if he finds it boring. I have to watch for the above mentioned signs to know even though I remind him over and over to let me know if he wants something different. I get him to sit and read and he starts off quiet but then he starts reading louder and louder and louder. If I'm watching tv or a youtube video and turn up the sound HE gets annoyed with ME and puts his hand over his ear facing me to make it clear that I'm disturbing him. Our life revolves around him and his needs like 24/7. Before quarantine at least we'd get 2-4 hours a day that my dad went to meetings with friends. On Saturdays he'd go out to the diner with his bestfriend for lunch. Now he's with us 24/7 and is ALWAYS around us. He calls me mom even though he knows I'm not his mom so idk what that's about and all day it's mom, mom, mom. My husband and I don't have children so the irony I'm now being called "mom" by my 83 yr old father seems especially cruel. Tomorrow I'm going to set him up with a book to read in the morning, we'll take a midday walk and then I'm going to set him up with movies in his room with his cat so my husband and I can get some much needed quality time together. I'm just so tired.

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D, I guess my question is, why did you all think that living g an isolated existence is EITHER daughter's home was a good idea?

Bback in the 1960s, my grandma would say "I'm so lonely" My mom would get annoyed and ask if she were chopped liver.

Ggrandma craved the community of her peers. Perhaps you dad seeks the same.
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My mom lived with me for 6 years and I did figure it out. I made a list of what I could do. Examples : go to Dr appts, make good meals and eat with her and hire a home health person. and handle finances with the help of an elder care atty.

I could not fix her and she was on the decline. I told her that if she was bedridden or ALZ I could not take care of her.

I had my own schedule. I worked part time. I had a small social life with friends and I gardened. I took her on drives and ate dinner with her.
She had three visits to the hospital and rehab. I had a good relationship with her Primary Care Dr. She had a DNR order in place, I had hospice and pallitive care phone number on speed dial. I checked out AL and nursing homes.
In other words,I managed the situation and hired help. When I need a vacation, I hired someone to stay with her which was expensive but I needed it.
The end of this story is that she had the best care and I learned the importance of
taking care of myself. It was not easy but it worked. Her money lasted and she did not end up spending her life savings to receive poor care in a nursing home or expensive AL. There were some programs but the paperwork would kill you.
Bottom line make the call to get more home health care with an eye on long term care which he might need.

I did my best and took care of important details but I hired help.
I used her money to finance this. When I looked into AL and nursing homes, they were too expensive and the care was iffy.
I did lose my freedom but now that she passed away, I know that she received the best care and my life has opened up again.
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It has been hijacked.

How did it come to be that Dad is living with you? Who thought that this was a good idea?
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Have you ever told him no?

Why do you have to gauge whether he is bored or enjoying himself? He can obviously tell you how he is feeling or what he wants, make him and stop trying to run his every moment. It's okay if he is just sitting and staring, daydreaming is a beneficial activity, regardless of what our teachers told us.

He is calling you mom to prove a point. If you treat him like a child he will act like one.

I know that your heart is in the right place, but back off and see how much better you feel.
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dwilliams927 May 2020
My sister was up here in January to stay with him during the day while my husband was in the hospital so that I could be there. She said the same thing. But then after spending 3 days with him she said she understood now. He can't be left alone. He gets bored and starts putting things away where we later can't find them, chewing his fingers raw, he sleeps too long during the day and then is up all night, he won't eat, he'll eventually come find me. One time I took an hour nap during the day because he had kept us up off and on all night and after he said to me "You were asleep. I didn't know what to do." Like if you were to leave a child alone. I think he thought I had gone to sleep for the night rather than just a short daytime nap. He knows I'm his daughter. He's called me his daughter to other people. But he calls me mom. Even when we were out at my in-laws last Sunday for mother's day. We were out in the yard in chairs so we could social distance but still see each other. He called me mom in front of my in-laws and they were surprised. He says it without any trace of irony. The "cruel irony" I was referring to is that we didn't have children and now someone is finally calling me mom but it's my grown father. He's not being cruel. The universe is.
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I think I understand a bit how you feel. I have been caring for my Mom with dementia but she did not live with us until COVID-19. She fell and fractured her wrist. I knew she could not live alone. After 2 weeks I realized I could not be her caregiver 24/7 and I was busy from day one thinking of options. Despite COVID-19 I did virtual tours of assisted living facilities because she needs help with everything and likes a lot of service. Her personality lifelong is very demanding and she is mean when she can't get what she wants fast.This precedes the dementia. I moved her to the ALF over 2 weeks ago and she is doing very well. She calls 10 times a day and I redirect and reorient her. I am using her money and she will likely spend down her limited assets but it's worth it. Even with COVID-19 she receives so much care and gets the socialization geared to her cognitive level. The staff at Bear Creek is so kind and very responsive so far. I still manage her medications and take her to Dr. appts if needed. When quarantine is over I will again bring her to my home for visits and on outings. The facility is following Colorado's state guidelines and they do not have any outbreaks.

No one can know another person's situation but I do know I have limits as does my husband. I do not want or recommend "giving up" your life for a parent because there are always options. Had I not tried to care for my Mother I would feel guilty but I knew I could not continue physically or mentally on a long term basis. I did try many of the things mentioned to keep my Mother's anxiety at bay and stave off her complaints of boredom. I did not want to have to drug her to keep myself sane.

I can tell how compassionate and dedicated you are to your Father. I know how hard it is to become the Mom. Consider ALF as even with COVID-19 many are still doing small group activities.
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There is only one solution here. It is likely that he is ni longer able to follow plot of movie or TV show. They never will tell you. He may no longer be able to comprehend reading either. My mother cannot make sense of a restaurant menu but again she won’t admit to it. She reads the paper every day as she always has but has now idea what she is reading. She also chews her fingers raw. You are not going to be able to give him things to do to keep him occupied for more than a few minutes. He looks just like your father but his brain is broken so he is forever altered. And I know it is difficult to cope with. The future is that he will continue to decline mentally and physically. After you get a better understand of what exactly this means by viewing videos and doing some research, you need to decide what you are willing to do. Soon it will not be save to leave him alone. Is anyone established as POA. Hopefully so. He may not be able to sign now. If funds permit, he will be better off in a facility where they provide stimulation and activities appropriate for him. Find one with option to move to memory care as he declines and needs that. There is nothing wrong with not wanting to take care of him in your home. It is a huge task. I am a nurse and I did not want to do it. We just went thru this with my in-laws. Fortunately they had money for their care. My FIL died yesterday morning at age 95. MIL last October.
Figure out what you really are willing to do and act accordingly.
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gemswinner12 May 2020
Dogparkmomma, my condolences to you and your husband for the losses you have so recently been through. My Mom died about two years ago, and now my Dad’s heart is failing. It feels like my world is caving in. I hope you and your husband can become stronger together; again, my deepest condolences.
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You should consider watching teepa snow’s videos on YouTube. Your dad has dementia & you don’t seem to understand it. He’s not calling you mom to be cruel. His brain is broken. You won’t be able to reason with him.
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dwilliams927 May 2020
I do but its hard for me to accept. My dad was an ironworker. One of the toughest guys I know with a larger than life personality and it's been really hard to see these changes in him. He doesn't notice it. He thinks nothing has changed and has stated that on more than one occasion. Yesterday morning he seemed to notice out of the blue and it shook him. But after a car ride to pick up Dunkin Donuts for breakfast (his favorite) and a shower he was back to not noticing again and arguing with me over handkerchiefs. I will check out those youtube videos though. You're the second person to recommend them to me. Thanks.
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Why do people allow their parents to live with them? In most cases, sooner or later the good relationships will be destroyed by the intruder - this must not be allowed or tolerated. Unless you can provide separate areas, DO NOT DO THIS...YOU WILL BE SORRY and you do NOT deserve this. Elderly people are very difficult with personalities and behaviors and mental and physical needs. Not everyone can or should be a caretaker without destroying themselves in the process. First, figure out how to make a separation since you seem to be stuck for now. Second, lay down some very hard, tough rules - and make them stick no matter how hard it is. It is YOUR home. He obviously has the beginnings of dementia and you better be prepared. Think about placing him if things get too bad. You will have no choice.
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truwoman May 2020
You may be right in some cases, but not all. My Mom lived with me for 25 years. She was fine mentally, but needed everything (and I mean everything) done for her in the last 6 years. She passed at 97, 3 mos, 9 days.

Just so you know it wasn't a piece of cake, in the last 6 years she was hard of hearing, blind, couldn't pass urine or feces, couldn't walk or stand, or feed herself, but she had a great sense of humor. I miss her every single day.

We got along wonderfully. She was worried about being a "burden", but I felt having her at home was easier as I didn't have to travel to sit with her in a nursing home.

We were 3 generations, my Mom, my daughter and I. We also had a home health aide a few hours several days a week.

I wouldn't trade those years for anything! Wish I had more!
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Your profile states that your dad has dementia. With this he likely lacks the ability to have initiative and it’s doubtful he’s calling you mom to be cruel. It doesn’t matter if he naps, reads, or is interested in movies. All those activities have changed for him and don’t need constant management. Most importantly, if the living situation can’t be made to work for all of you, a new plan for his care needs to happen.
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dwilliams927 May 2020
My concern is when he's bored he chews his hands. In the past his hands got infected from chewing and he had to be hospitalized. Yesterday, I found he gnawed most of the skin away from his nail and there were actual striations IN the nail from his teeth constantly gnawing at it that it was wearing through. And if he sleeps during the day then he doesn't sleep at night and he paces the house and makes a racket waking us up. I spoke to his doctor about the nail biting today. It's an OCD behavior. When I put neosporin and bandaged the finger plus applied neosporin to a couple other spots he couldn't bite his hands anymore and instead switched to trying to shove his fingers in his eye to "open it" even though it was open. Hopefully the new medicine will help him be less agitated and in turn *I* will be less agitated as well.
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I don't think I provided enough information in my original post. My dad was diagnosed with Alzheimer's in January. He had "mild cognitive impairment" and been living with my sister in his own home. He continued to decline and his GP put him on me meds. I realize during my visits that he was skipping pills and dropping them on the floor and so I put my sister in charge of his meds. She took 3 months off for a worker's comp injury and that's when we noticed his symptoms worsened further. Despite that, my sister decided to go back to work anyway when the 3 months was up. She said "I have to do what's best for me." A few weeks later I got a call in the middle of the night from him sounding scared and confused and vulnerable. I picked him up first thing in the morning and brought him to our house where he's continued to live. I love my dad. It's just frustrating how quickly our lives have been upended and the quarantine has only made matters worse.

I know calling me mom is not meant to be cruel. Nor is he trying to send any kind of message. His doctor believes it's because I've had to take on the caretaker role and it's easier for him to associate me as his mom in those moments than as his daughter. The fact that I never had kids and have someone calling me mom who is NOT me kid is the cruel irony I was referring to.

I understand Alzheimer's but I get frustrated. I'm not mad at him per say. I'm mad at the illness.
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