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I look at quality of life. Being stuck in a bed barely moving, barely able to open his eyes and medicated for extreme pain. What type of life is that? The only interaction is changing briefs, bed linens and given meds. He might not be aware of that.
The surgery alone could kill him given his weakend state. What about the anesthesia alone?
I was given that choice for my dad. They said he could pass from the surgery, but wanted to do it. Why? So it could prolong the nothingness that has become his life? Basically sleep 24/7. Doesn't hear the tv.  Doesnt know if its day or night. Or respond to anyone. I said no. I know I wouldn't want to live that way. 
The medication takes care of any pain. The body systems start shutting down. 
I've taken care of people in vegetative states. I know what goes on. I think it ties back into the dnr. I could understand if he was talking, alert at times, and able to interact with his surroundings. 
My mom stopped eating over time. She wasn't in any pain. She was able to verbalize if she was hungry. It is a natural part of the aging process.
You don't need to feel guilty for anything. You are there for him. 
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If I may I would outlaw the tube as it is the most frightening experience for a person who can object but patients without cognizance it is death and discomfort. Hold my hand till I die, keep the patient at home and cherish the last days.
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One of the final stages of dying, from what I have read, is that the patient refuses to eat. Refusal of food, for the dying, is very strong. We tried to somewhat pry open my husband's mothers lips just to get some apple sauce into her. She knew what we were doing and adamantly refused keeping her jaw as closed as a vice. I was even surprised at her strength in keeping lips together. When it comes to that time in the process of dying, or near the finality of living, a feeding tube would be so much against what the patient wants and would only extend their misery. Hang in there. You are doing the right thing by going to Hospice. They are a wonderful resource with which to endure the last days of living for, not only the patient, but for yourself.
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My mother started on hospice services at her facility last week. She barely eats, and gets angry if you even so much as offer food, has lost a lot of weight, and the nurses suggested having her evaluated by hospice. The first time they came mom herself said no thanks, but then again she has dementia and of course thinks she is just fine. The next week they didn't ask her, they asked me, and did a more thorough exam and determined that yes she is a candidate.
These people have been a blessing. They help me to understand the dying process, including the loss of appetite and weight loss. They offered chaplain services. I have access to help even if just to talk 24/7.
My mother is still active, dresses herself, feeds herself (the few bites she will eat), and is able to carry on a conversation, but has no idea of time or age or location, and no short term memory at all. So she is in the transitional stage, not in the actively dying stage yet.
Hospice does not always mean that death is around the corner. The folks that help me have other clients in my mother's ALF that have been on their services for well over a year.
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Oh you poor, strong loving daughter. You are in a tough situation, thankfully your dad gave you his wishes when he signed a DNR, he doesn't want to live quantity with no quality, that is what most of us think of when making the DNR decision.

Love him, be there and be thankful for his thoughtful forethought. I had a friend that was basically unresponsive in hospice, I sang to her, put lotion on her and told her it was okay to let go, she is loved and will be missed. I believe it helped her and I know it helped me say goodbye with all the love I felt for her.

I pray that you find peace and know that you did a loving, generous thing by not prolonging his suffering. God Bless you and give you strength on this difficult journey.
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My mother has been in hospice for three days now. It’s a hard decision, but one that I know is best for her.
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My Mom was under hospice care and passed away 3 weeks ago. She suffered from Parkinson's and dementia. She went pretty quick. She started declining one week and the next Wednesday she was asleep. I felt like we were starving her but her body naturally was shutting down. She would not have wanted to live like this, which is why she was DNR. I don't know that anyone would want to live in that state. Mom was getting no medication whatsoever, only oxygen. She went peacefully early on Friday, 05-18-18. Know that you are doing the right thing for your Dad. Let him be free. I miss Mom everyday but I take comfort knowing she's no longer trapped in her body.
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Read a book called "Being Mortal" by Atul Gawande. Good discussions on quality of life versus just living. Hospice is the kindest route for those with terminal illness.
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I dont think i mentioned this before but even if i have i'll send the reminder again that there is pallative care which is different from hospice and something you can check into.
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The original writer, passingfancy, hasn't return back since writing this question 12 days ago. Hope everything is ok.
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Hospice can be the kindest way to let your beloved Father go in peace. Please be at peace yourself. Bless you.
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