Day 7 no food or water
It is just so painful watching the days tick by with only sleeping and changing him. His changes are now 4 hours apart because of so little fluid coming off the different organs. In spite of a low-flow mattress he managed to get a new bed sore. The skin is just breaking down and when I start to change him he starts scratching. I try to stay busy doing anything else. Packing to go stay with my daughter for a few months if this is ever over. He reaches out for a hug and those will be such sweet memories.
Comments
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so sorry. You are on a long vigil. Are you by yourself? I hope your daughter is there. I read somewhere that caregivers need a place to go and debrief after caregiving.
Going to your daughters seems like a great idea.
You’re in my prayers.
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My heart is with you.....I well remember the days that seemed to go on for what seemed like more than 24 hours.
-Judith
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Hugs hugs hugs hugs
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(((((Lgw)))). I’m so sorry
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Sorry for such a difficult time in your life. I think staying with your daughter is a good idea, but you will likely need some time to just be alone with your thoughts. I hope you have someone to be with you now.
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We are all thinking about you lgw.
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My grandson and his wife are living here. The greatgrandsons keep me distracted. Here goes day 8
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Little ones can deflect some of the agony. Surely this will be one of the longest days. Hoping he and you will have peace at the end.
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Praying for you and your family 🙏
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Lgw, I’m so sorry you’re having to go through this. My heart goes out to you. My prayers are with you and your husband.
Brenda
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I am thinking of you and sending a soft hug your way.
J.
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Lgw sorry this is surly the hardest time sending prayers you.
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on day 10. looks like he will make it to day 11. No pee left
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I wish I could comfort you. I just hope he's comfortable.
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Lgw glad you have family there with you but sorry you have to go through this. Sending prayers for peace and comfort to you, your husband and family.
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Thank you for taking the time to update. What a vigil.
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Praying for you.
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Lgw Thinking of you during this difficult time. God bless you and your family and LO
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Lgw - sending you hugs and prayers. I just can't imagine how difficult this is for you.
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Thinking of you, and sorry this is so extraordinarily trying.
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Praying for you and your family. I’m glad you have someone staying with you during this horribly difficult time.
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Praying for you and hoping that your DH will soon be at peace.
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My DH has made it to day it to day 12. He woke me up breathing really hard. Figure he was in a lot of pain. I got up and gave him his morphine and he relaxed. It is so difficult to change the chucks as he is very rigid. At least he no longer wears a diaper the normal way. Just tucked behind him so that is easier. We are still peeing at the rate of 2 times a day. Anyone else faced this? I try using the draw sheet to turn him but I'm just not strong enough. The Hospice nurse now comes 7 days a week, and the chaplain now will come 3 times a week if he is still alive. I am tired. It seems too cruel to ask for respite care at this point. He wanted to die at home.
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Prayers for you and a peaceful passing. Hugs
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Lgw,
I am so sorry you are having to endure this agony, knowing the outcome. My DH was “struggling to breathe” with an oxygen level at 82% on Tuesday afternoon, when I was advised to notify family members. Additionally, however, he had vomited that morning and developed aspiration pneumonia, I believe. He was exhibiting noisy rattling and gurgling as well. He was administered medication to dry the secretions and quell the rattling; it did help somewhat. I stayed bedside from Tuesday afternoon until he passed on Friday evening. I “think” I recall a few, very few, changes of briefs and a hospice aide bathed him thoroughly once, on Thursday. By late Friday afternoon, early evening, his breathing rate had dropped considerably and my son began timing his breaths. He was breathing at about 5-6 breaths a minute and the facility nurse said she was going to give him medicine (morphine and Ativan) for agitation; I didn’t think he was agitated. He then passed, very peacefully, in a very few minutes.
I am so in awe of your decision and perseverance in keeping your DH at home. I thought I would do that; I did not. I am comforted by the care and compassion shown to DH at the MCF; it was as close to home as I could provide. I pray this journey will end peacefully and soon for both you and your DH. You are a rock; I admire and envy your strength. Bless you!
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I’m very sorry for these trials and heartache. So very hard.
When I was assisting my mom with end of life care, the hospice nurse and CNA came by and asked me if I wanted them to change her. I said no, don’t rattle her. This was on day 7. After chatting for a bit about things, they encouraged me again to let them rustle her a little by changing her because sometimes a body shift, lung shift, organ shift can allow for something (can’t remember exactly what it was) that might allow her body or brain or heart to finally give way for her to pass. I’m going to ask the nurse again cause it made sense at the time. Not sure if it helped mom but that’s what they said. She passed on day 8.
Also, as far as the meds, I was giving her morphine, haldol and lorazepam on a schedule, round the clock. She didn’t show signs of discomfort or rigidity, only rigidity in her last couple of hours. Morphine was every 4 hours with no sign of discomfort. I asked the nurse if I should stop since mom seemed unavailable in any way, nurse said absolutely not, err on the side of comfort.
im sorry this part is so difficult. Please take care of yourself too. Give yourself lots of time.
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Thinking of you..............
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Praying for you.
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Now day 13 he is in a coma and now the death rattle... I was afraid to write anything down thinking it would make it longer. He deserves to go to heaven soon.
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Holding you close in prayer and sending virtual hugs.My heart breaks for you.
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Commonly Used Abbreviations
DH = Dear Husband
DW= Dear Wife, Darling Wife
LO = Loved One
ES = Early Stage
EO = Early Onset
FTD = Frontotemporal Dementia
VD = Vascular Dementia
MC = Memory Care
AL = Assisted Living
POA = Power of Attorney
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