← Return to Moderate Alzheimer's, Frequent Resting and Napping

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@billiekip

I'm assuming you don't feel comfortable going to sleep first and leaving him awake. No telling what shenanigans he might get into. The number of hours my husband (ALZ) clocks is astounding compared to my measly 7-8 hours if I'm lucky. He goes to bed by 9p, up for breakfast about 10am and then goes back to bed. Yesterday he didn't get up until after 3pm. He has no trouble going to sleep. The only RX he takes is mirtazapine, an antidepressant. I'm not sure if it is his brain needing to be reset; or he just doesn't see any reason to be up. He has lost all interest in any activities. He always slept way longer than I did; but this is extreme. I've been having some pressure about moving him to a memory care facility. He tells me he is happy here and feels he has had a busy day even though he hasn't. I'm staying the course for now. I think your feeling tired is more about the emotional drain this disease puts on the caretaker than the number of sleeping hours. This is tough sledding.

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Replies to "I'm assuming you don't feel comfortable going to sleep first and leaving him awake. No telling..."

You've hit the nail on the head with alot of what you mention here, especially about the emotional drain this is taking. I toured a memory care facility a short time ago and have decided NOT to place him and getting in-home care instead. It it is mainly for respite care. My Tom (63 years old) tells me he's happy here also, and i'm the bestest 😉 I've had to adjust to ALOT and will keep doing so as long as I can, and his sleep patterns are just another adjustment that we just keep moving along with. I am so glad to have this platform to share with and get advice or just say what's on our mind. Because a lot of us I'm sure have gone through or going through a lot of what is being posted here and I am so thankful for this community! I am only 59 and never thought I would have to be going through this at my age.
I appreciate you as a (struggling) caregiver AND the Mayo Clinic for allowing us to share with other caregivers.
Strength and Courage