Not sure if I posed this question correctly but:
I was just given a book to read about dying and the work that hospice does in support of that. The first case I read about had to do with an 83 year old woman dying of cancer and her attempts at saying good bye to her husband. It appears that because she had all of her faculties, she was able to do this. It also described the reaction of her husband to this.
In the case of a person who has dementia, what kind of “closure” is there during the process of dying? What is their process for saying goodbye and what reaction will their caregiver have as they are actively dying? It seems that the cruel disease of dementia also robs them of their dignity even in death. Do any of you have any thoughts you can share in terms of your experience with a dying loved one with dementia?
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Mom was 96 and lived with me and my family for 6 years. During that time she went form being able to stay alone and function pretty well to me being her more than full time caregiver due mostly to dementia. It is cruel and horrible to watch. It broke my heart to see her look blankly into my face, and yet there were days she would know me and be able to visit. She would see things/people and before she was in the wheelchair she would "want to go home" so I would have to follow her throughout the house to make sure she wasn't getting out on me or do something that would injure her. Anyway, in our case she would not eat for me one day. At first I thought it was a short term thing. But the next day I called her doctor because I was worried that she would get dehydrated. They were not extremely concerned and told to keep trying the things I was but when she still would not eat or drink the third morning I took in to ER. They were going to re-hydrate her and maybe keep her a day til she would bounce back but then within the next 20 minutes they came back into the room and said her numbers were so wacky that they were not sure she would bounce back. I went from being elated she was getting fluids via IV to looking at bringing her home with hospice. She came home on Tuesday afternoon and passed away on Saturday am. She slept most of that time. She would open her eyes when we would turn her and I think she knew us and was at peace, My brother was not able to come and i think she hung on until I finally was able to tell her that he wasn't able to be here but he sent his love and it was ok to go and be with dad in heaven. I struggled with that only because I didn't want her to go even though I think she knew it was time and that is why she quit eating for me. I am sure everyone is a little different but I think with dementia they are at peace and you can still say your goodbyes and talk with them even if they cannot or do not say much. They feel the love, and I know it helped me when someone said I should tell her its ok to go. My friends mom waited until her brother, who didn't want to be there finally came and at least said he loved her. She just needed to know that and passed within hours of him visiting her. After my friend told me that and I got up the nerve to say that to mom about my brother she seamed to also let go and was ok with it. I hope this helps. I miss my mom so so so very much and I am in the process of figuring out the next chapter in my life since she is no longer in need of my care giving. I am looking for a job and trying to move on.
My husband on the other hand is barely aware of where he is, time of day and who is in the room, and has difficulty swallowing. He is totally incapacitated mentally and physically, can't walk, talk or write any kind of instructions. He had this talk with me a couple of years into his dementia when he still could make lucid decisions. As his POA and now guardian, I know what his wishes are. He took each of our grown children aside and talked to them, expressing love and apologizing for anything he may have done or omitted. That was about seven years ago. He is in the final stages of FTD. If he stops breathing or his heart stops I know that DNR is the way to go, if he gets pneumonia to not give antibiotics, if he gets another life-threatening disease to just keep him comfortable.
As his wife and primary caregiver, I am keeping his dignity intact by following his wishes as he slowly slips farther and farther away. I am saddened to watch his dementia take him away, but he is in a place now that he doesn't realize what he used to be and he no longer mourns his former life like he once did. This life is the only life he remembers clearly.
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The thing is, nothing in life is ever going to be perfect or work out exactly how we want it to work out, and you cannot hold on to some UNDESERVED guilt in spite of the fact that your husband was FREED without you standing right beside the body that he was freed from.
Don't mean to be preachy on ya and please forgive me if I sound that way. You see, in writing this to you I am also writing it to myself. We gotta quit this guilt stuff and move on. Right?
Anyway, you are not alone and what you have felt and what you have experienced has been felt and experienced by countless others and we need to allow ourselves forgiveness from ourselves ... for we are the only ones blaming us. Your hubby doesn't and neither does my Dad.
HUGS!!!
I think that accepting that he was dying was tremendously helpful to me, and probably to him. No one was anxiously trying to "fix" anything, but only to keep him comfortable.
I wish I could have been there for my dad's passing like I was for my mom's, but with dad at least I knew we had already said all the important stuff and the people with him loved and cared for him too. They also couldn't quite tell me how bad it was and it sounded so routine earlier in the week...I would not have gotten there anyways if they had told me even as much as 12 hours sooner, that was the reality of it. Once I knew, I got coverage for my weekend at the hospital where I work, but found out about 2-3 hours into a 15 hour drive in the snow that he was gone...
In my limited experience, a dying person seems to be already gone long before the breathing stops. If you can be there, that's great, but as almostthere says, "Nothing in life is ever going to be perfect or work out exactly how we want it to work out." Let's not put pressure on ourselves or our loved ones to die according to any sort of rules.
End of rant.
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