We just moved Grandma in 1 month ago. I am so new to this. I am actually an RN, but nursing school was 20 years ago and we did not learn how to live with our elderly grandparents. Our geriatric rotation was 5 hours and then we got to go home. I can do anything for 5 hours. A 93 year old 24 hour confused room-mate is harder.
I feel like the only reprieve I get is when her caregiver is here in the morning for 3 hours (I escape to the gym), or when I am working, which is not all that much of a break!
It's the dementia that is making it so hard. She asks the same questions over and over, and she hardly ever stops talking!! Sometimes I just have to ignore her because I feel like I will lose my mind if I tell her one more time that yes, she did have lunch, would she like a snack? I don't remember her being this chatty when I was a kid. She wants to talk non-stop. If I leave her to do laundry, dishes, dry my hair, clean her room (you get the picture), she gets all weepy and tells us she is in the way and we should send her to a nursing home. She actually isn't in the way (and we tell her this over and over), but we cannot sit and visit with her all day. I have stuff to do! I did remind her of her crochet project and that helped for a couple of hours. And I had her help me with a sewing project I am working on (even that was hard, I asked her to rip out 2 seams and she asked me at least 10 times if I wanted her to rip out both seams. I finally wrote "rip out both seams" on a piece of paper but she was still confused). THIS IS SO HARD.
We know her days are limited and we want her to feel loved and wanted, and she was just wasting away in her retirement community because her mobility has become so limited. She wasn't leaving her room. She lost 30 lbs in 6 weeks. Every time I went to see her she was sitting in her pajamas alone watching TV. We take her out almost every day. Yesterday it was just a walk around the park in her wheelchair, but she got out. Today she got her nails done. I know for the most part she is really happy here. We have kids and a lot of activity.
OK, I feel better. Just needed to vent. I don't have anyone to vent to. My mom is racked with guilt because she didn't want to move her in with her, and my sister has a million kids. So thankful for this forum. And wine.
You are absolutely right: It is the dementia, and THIS IS SO HARD!!! It is hard (in different ways) whether it is your grandmother or your father or your spouse, and whether it is Alzheimer's or Vascular Dementia or Lewy Body Dementia or some other kind. Caregiving for someone with dementia is HARD!
It sounds like you are doing an excellent job, in spite of how hard it is. I'm glad you get the 3 hour respite in the mornings.
This isn't going to last forever, but it could last a few more years. Pace yourself. Be sure to arrange to take some vacations.
Would it be possible to get her active in some kind of senior daycare program? It would be a few hours each week that would allow her time to socialize with others her age. Another option is to give her a daily set of "chores" to do. My mom and dad both have severely limited mobility, but they both have chores they do on a daily basis. Dad gets the newspaper in the mornings, checks the mail and is in charge of making their morning coffee. Mom washes their dishes in the morning (usually just 2 coffee cups and 2 small saucers) and makes up a grocery list of anything they are running low on. (I do all the shopping, but for example, I don't drink coffee, so if they're about to run out, I wouldn't even remember to check it most days!)
It's not much, but it gives them both something to look forward to doing each day that they are both used to. Dad used to wake up early for work, and he loves being able to go take mom her morning cup of coffee, while mom loved clipping coupons and making the weekly grocery list.
Another option would be to look into a 'sitter' type person for her. Someone that could just come over daily or weekly and sit and talk with her, or just be with her while she watches tv or reads, or (if she's up to it) could take her on walks around the block while you get things done at home.
Just wanted to say "welcome to the board" and - I am only a part time caregiver to my Mom and by the end of the week I am ready to pass her back to Dad but I do have a teen with special needs and she LOVES to repeat things over and over again. (OCD-constant need for assurance) And it is hard and yesterday I locked myself in a room in the house and just bawled into a pillow and this is my daughter! I mean , I am her Mom and should have better patience than that but --it just gets to you!!!
TardisTT -gave some good ideas-- wish I could give you more. Just know you are not alone and this is a good place to vent. Good luck!! And welcome! (((hugs)))
I am sure you have tried music.
There is a toy parrot that mimics your words. It is fun to play with. Maybe get him one and see if it will amuse him long enough and perhaps fill the need for constant talking without having you right there --again-just throwing it out there.
Good luck!!!
I understand the frustration and you came to the right place!
My Dad had dementia and he had a limited ability to focus on any one activity and was obsessed with checking his watch and stating what time it was. I found his impatience annoying in the beginning but I eventually found things he liked to do for short periods of time...we used water colors and painted, played a lot of card games which would start off as a game but would end up with him making up his own game. This drove my Mom crazy and she would scream at him. I found it funny and played along with him letting him take the lead. It took awhile to be able to accept it was the dementia that caused the repetitive questions and frustration for him when he couldn't verbally express what he meant to say. I think remembering that they are losing themselves makes it easier to be patient. I once told my Mom to think of him as a stranger she just met because long ago I learned we are often harder on our own kids then we would be on a visitor or someone else's child.
You will find peace within yourself and really let yourself enjoy the time because it goes quickly. Find your inner humor and find her humor if possible. Crazy little faces and exaggerated gestures would make my Dad laugh. He was not one to laugh very often so when it happened it was awesome and a memory I will never forget.
You need to take breaks when possible without guilt! We all have lost our tempers and yelled and wept with exhaustion it is ok. If you focus on a positive moment each day I found it gets easier.
Hang in there and venting is critical so you won't lose your mind!
Hugs and prayers to you and your family!
I try not to stop her when she is in a chatty mood because I know she gets lonely. Trouble is that I start feeling rattled. But then I feel terrible if I tell her to stop talking. So I just let her talk and try to tune her out if I'm doing something. Sometimes I wish we had an on/off switch on our ears.
It sounds like you are a very caring granddaughter. Your grandmother is a lucky woman. She probably knows that.
Bless your heart.
I too am a nurse. I cared for my dad in my home for 5 years and other than knowing all about his medical conditions and what his blood tests revealed I was a daughter first and a nurse second. I think that's just the way it is. I was able to troubleshoot and clean and dress his leg ulcers but my emotions were that of a daughter, not a nurse. When I'm at work there's a professional distance we don't have with our loved ones.
And while I cared for my dad in the past 5 years I cared for my grandma in her home 17 years ago while I was in nursing school. I was there weekdays and my cousin was there nights and weekends. Reading what you wrote brought it all back.
The chattiness is from the dementia. As you know, dementia is a disease of the brain and while we have filters, your grandma may not have a filter anymore between what pops into her head and what comes out of her mouth. My grandma had Alzheimer's and I can't tell you how many times I cringed when we'd go out. She'd comment on the waitress or other customers. I had to ssshhh her all the time.
I think your grandma's in good hands with you. A busy, bustling house may elevate her mood and make her feel a part of the family. I know how hard it is and dementia would test the patience of a saint so don't be too hard on yourself.
You can hire a 'sitter' through an agency. This person literally comes over and just sits with your grandma and talks (or listens as the case may be). I don't know if something like that is in your grandma's budget but if it is it would be well worth the money. No, you can't sit and visit with her all day. I don't remember if your post said how long your grandma has been living with you (maybe I have dementia too!) but if it hasn't been too long give her and yourself a chance to get into a routine. She may be chattering away out of nervousness. The suggestions about finding something for her to do are good ones and there's nothing wrong with plopping her down in front of the tv if there's something on that catches her interest. You don't have to entertain her. Can she fold towels and linens? Just keep washing them over and over and bring them to her to fold. Can she cut up green onions? We did this with my grandma. She wasn't real capable of cutting up much but green onions were a snap for her and she felt needed. We had a lot of green onions! How about getting some Lysol wipes and asking her to wipe down the kitchen? A task like this would take my grandma an hour and that's how I cared for her, in increments. One hour at a time. And what might have kept her interest on one day may not have kept her interest on another day so we were constantly looking for things to keep her busy. Photo albums are always a good distraction.
My grandma was a talker too. I remember the day of the O.J. Simpson verdict. The entire country was on pins and needles, me included, and I was glued to my grandma's tv. She kept yammering on and on while I was trying to listen to the verdict. It's funny the things we remember.
With dementia you have to be creative. We can't expect our loved one with dementia to completely be a part of our world anymore so we have to crawl into their dementia with them. Oh! Junk mail! I would get my grandma's mail and give it to her and that would occupy her for a while (after I removed bills and things she could obsess over).
Good luck! I only found this site a few months ago and my dad died almost a month ago. I so wish I had found this site sooner. You're in good hands here.
I am trying to think of things to keep her busy, and I would love if I could give her a chore (she says at least 5 times a day, "Is there anything I can do sitting that would help you?"). Along with dementia she also has pulmonary fibrosis and is attached to oxygen at all times, She can't take more than a few steps without becoming hypoxic. It's definitely a challenge.
Take care - and be well - have a good weekend - enjoy the spring!
Sounds like you are doing a wonderful job!! It is so difficult when you are the only caretaker. YOU need to take care of YOU too!! This is very important! I would call your State or city , Center for Aging, Church or even the VA or VFW, American Legion. There are programs out there to help. To come in and sit with
her for a while. God Bless you, you are doing a great thing. These facilities, nursing homes do not treat our loved ones as well as we would. Hang in there.
There is a bit of resentment too...Both my Mom and my Uncle's retirements have been postponed because they have been financially supporting my Grandma for the last 3 years. They set her up in a beautiful retirement community with a HUGE rent. Now that she is requiring more and more help, she was not using the facilitiy's amenities, AND they were having to pay more and more for a private caregiver to come in. It was totally draining them. My Grandma also wasn't thinking about the repercussions of some of her actions. She wanted a burger for dinner, so she didn't eat what the facility was serving, called her caregiver at 9pm and asked her to bring her a burger. That burger cost my mom $50. It also wasn't cheap when my Grandma was curious to see if her Life Alert worked in the game room. It did. $350.
Anyway, I am doing this for my Grandma and my Mom and my Uncle. They send me money to pay for a caregiver to come everyday to help with her shower (I do it on Sundays, I like to keep an eye on her skin and such). They said they will send me more if I need more help, but I am trying to hold out for a little while. I will ask for it when I need it.
Anyway, That is my story.
I have been in her shoes...no help no place to go. If your having a bad day, just remember...It is the disease. Try and think back to better days. :).. I treasure the days I have with my father, good or bad! Good Luck and God Bless