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I'm sure that you will still be doing Plenty of caregiving, just in a different way. Now hopefully, you will have some time to enjoy him, and to spend quality time with him, when you are not Always Burnt Out!
After he becomes acclimated, hopefully you will be able to take him our for a few hours here and there, but I'm sure you will still be doing plenty of running around for him, and it will still feel like work for a few months.
Do not bring him back home, it would be a big mistake! Your LO's needs are only going to become greater, remember that!
Good Luck, it's time for some ME TIME! ENJOY IT!
Guilt seems to be the background reality for caregivers. No matter how hard we try, we are never going to be able to fix our loved one, and somehow we think we should be able to. This sense of guilt is irrational and unearned, but it is extremely common. If you can't overcome it completely, at least push it way to the back of your mind, and don't let it influence your decisions.
Ten days is way too soon for anyone to settle into a new environment. And dementia can make it harder. Hang in there!
10 days is nothing in the scheme of things. It's just so very fresh to both of you. Adjustments will be made, it's kind of how it works though it's so very difficult. It's no fun at all and I endured 7 years of it with my mom.
I can't say it will get better. Manageable would be my word as far as my mother's experience. She wouldn't participate in any activities so she was always pretty negative.
Your words "that you feel guilty causing this" struck me. YOU did NOT cause this situation. The disease did this to your loved one. The blame lies with the disease and its' awful affects, not you at all.
I realize you were describing the change in living situation, but that is what it is, living. You deserve to live without horrible, unmanageable stress that makes you ill too.
Prayers for more peaceful days in the future for you and your LO.
My husband has been in the AL for 6 weeks now and he is still not adjusting well. I have been seeking therapy for that much time to cope with my guilt and sadness, and I am not progressing well either. The AL is also making errors, so that adds another layer of grief to my plate. I am seeking an alternative care option and I am moving towards home care with adult day care during the day while I am at work and night health aide so that I can sleep to go to work the next day. Interestingly, the cost is less expensive than at the AL.
I don't have sage advice for you, except that you should take this opportunity to explore other care options. Remember that there is no perfect solution. Choose the one that works best for you under the circumstances and give it a shot. If it does not work, then try another option. If you don't try, you may look back later and regret it.
Feel free to share any tips you have with us. We are here to learn too.
Regardless, only you can know if you made the right decision. Lord knows, you don't need guilt right now. Sometimes our best intentions don't work the way we thought and hoped. This is why I never promised to keep my LO's out of a NH. Because I can't predict the future.
I am currently taking care of my 96 yr old DH and he is still at home. He has "age related memory loss" but not dementia.
I like what WorriedSpouse has suggested. We all still have many options at our fingertips - we just need to know what they are.
I will continue to keep my DH at home as long as I can. But I try to remember there are many options available and we just need to find out what they are.
Praying you find the right decision for you.
Blessings to your family.
So, yes it is heart-wrenching. But HANG IN THERE! If you were at the end of your rope, you HAD to place your loved one! It will be rough seas for a while, but drop anchor, hold on tight,you will be ok!
I agree with the person who said, visit often - and I would say, notice the timing of facility activities - and maybe do a couple of activities with him, and join him in the dining room - (even if it's a bit hard). And when you leave, tell him how glad you are to see him looking so well. Notice any good things. In other words, you commit also, to valuing this opportunity, keep your questions to yourself. Let him see you are glad to have help, that allows you to visit without being overwhelmed. If there are any shared activities you did, like reading or music, TV shows or movies, see how you can enjoy them there - like buy a DVD player and share reruns with him.
Without trying to overdo, or make suggestions too much, notice what's there to enjoy and do some with him, or notice people in them. In other words, make the facility part of your new network, that still includes him. In my brother's nursing home, they regularly get the best musicians, I'm jealous - there's lots of talent that continues to work by assisting or volunteering at such places. If you spend an enjoyable 2 hours visiting him, then gladly say bye for now, I'll be back on Thursday.... maybe 2 days later - you can be supporting his transition in the best ways you can - and then wait.
If after more than a month, you feel wrong, then look for alternatives, but for now, you've made a commitment, and the best thing you can do is give it a good chance, as there were many good reasons for that commitment!
This last year, my husband developed high blood pressure and I was always fatigued, sleepless, stressed. The moment came when I had to make one of the hardest decisions in my life, and for the sake of my marriage and our health, I made it.
Mom has been in ALZ facility or 5 months now. The first 3 months were difficult as she asked to come home daily. I had to explain to her why she was there - her physical and mental issues that I could not longer take care of - many times each day, as she would forget and call again and again. This was very hard. The staff at the facility is very good and cares for her, but my Mom is not very social so she will not enjoy the activities there....I finally realized this is her choice and no one can push her.
Now, the reason I am writing you is that on the 4th and 5th months, Mom has adjusted somewhat...to the point that when she now asks to come home a couple of times a week, all I have to repeat to her, with love, for her to understand and accept is:
"Mom, remember that a year ago you told me that when your care got too much for me to handle, that I should find a good nursing home for you? Well, this is the best in the area. Remember I could no longer work or spend time with my husband?"
Mom then says to me: "Yes, you did the right thing. They take good care of me here. They are very nice."
I hold on to this answer until the next time she asks to come home, or why am I here, or the doctor has not seen me today - she continually thinks she is in the hospital, and other times she thinks she is at home and that I sleep in the next room.
It is a cruel disease. It is sad. I have had to accept her karma and do the best I can to call her each day and to visit her 2 or 3 times each week. I have had to learn how to choose myself and my life instead of sacrificing all my energy to another. I am learning balance and so will you. Stay your path and do not bring your LO back home yet. It takes time for them to adjust.
All the best!
At first, like you, I felt guilty, in spite of the fact that she became unmanageable, even hostile, while at home. She has calmed down considerably at the facility.
I don't know your circumstances, but I can ask what would happen if taking him back caused you stress that brought on a heart attack or nervous breakdown. What would happen if you were killed or disabled in an accident? What would happen to him in such events? What about some disaster like a house fire that required fast evacuation? We have no such worries if our LOs are in an ALF.
I wish you the best.