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let the caregivers give and do their job; your role is to be the loving and supporting family member, spouse, sibling, et al, and to be their advocate .
This way your valuable time to spend with him loving, friendship, support. I’m finding out, it is tough to do both 24/7…indefinitely..
maybe now is the time for me to listen..
I understand so much more now.
You, as caregiver spouse just MUST be able to get some rest.
I would take this concern to his MD because you won't be long able to continue caregiving if your hubby is up raising the kitchen all night while you try to recover from your daylong caregiving with a bit of shuteye.
The problem here, of course is manifold. If too strong a med is given to someone suffering some dementia it can complicate things enormously. Some meds have the opposite effect wanted, some cause falls, and etc.
I am hoping, after consult with hubby's doc, there is something light that can help him sleep. For my partner one half a low dose benadryl does it. For me, benadryl gives restless legs and sleeplessness. Go figure.
Afraid you are in for some experimentation to figure what will safely work.
Eventually, if things progress, I know that you know that you will be limited in being able to be 24/7 caregiver. I sure do wish you good luck and hope you'll update us.
Medications that result aiding sleep can also create a fall risk if the person does get out of bed. And some result in what I call "brain fog" and the last thing a person with dementia needs is more "brain fog"
Is your husband in a hospital Bed?
**If so you can try bed rails (I know not allowed in facilities but can be used in home)
**Placing pool noodles of pillows under the sheet along his side might make it more difficult for him to get out of bed.
**If in a Hospital bed you can also try lowering the bed so it is more difficult for him to get out of.
**Trying to keep him active during the day may result in him sleeping better, longer.
**Placing a door alarm (looks like a wedge door stop) by the door would alert you if he got out of bed and opened the door.
Honestly I would be less worried about eating and moving furniture than I would be concerned that he would walk out of the house on some "quest".
Due to your fragile health it might be time to seriously consider placing him in a facility that can safely meet his needs.
You do not need the stress, worry, lack of sleep that goes with being the caregiver of a person with dementia.
“Any advice? I am wiped out and even had a small heart attack. Waiting for test results now.”
Oldstew, I am so sorry! I hope you can find a good answer to the nighttime wandering AND protect your own health. Thinking of you.
an hour before bed.. or a bit more:
Ensure, 2 scooos if whey protein, ice, frozen berries..
blend it.. it’s a fun desert.
I have a Trader Joe’s near me. Frozen mixed berries, frozen fresh fruit..
I finally realized I should only take anbuen once I am in bed. I dont wonder so much now. Family has woken me up in the tub. Used to raid the kitchen and didn’t remember. One morning my mouth felt all gritty.. yup, apparently I was eating trailmix then knocked out. I felt like a squirrel that morning. My cheeks were not completely filled, but definitely had trail mix during the night. I have a friend in another country, so I’d call her and fall asleep. I did this multiple times.
Do read the warning labels and side effects.
Getting off balance and falling can be high risk.
I’ve been in this stuff way too long, I feel I can’t sleep without it..
so … think about what is manageable will it actually improve his sleep pattern?
Serequil (?) for sundowning, I believe was given to mom… this was a few years ago.
ALZ just sucks. Not fun.
I’m actually surprised that there is so little acknowledgement about how common this is.
https://www.health.harvard.edu/blog/cannabidiol-cbd-what-we-know-and-what-we-dont-2018082414476
Speaking for myself, I am more interested in a good night's sleep and a reduction in pain/anxiety than I am in absolute "safety". (At age 86, there's a minimal chance of premature death.) Of course, I don't agree with elders being "drugged into oblivion", which sometimes can occur, but I support the concept of meds at the right time for legitimate reasons. It's a balancing act.
While it may seem--well--almost abusive to 'drug' a LO into a good night's sleep--think about the poor CG who never really sleeps b/c one ear must be kept open to listen for sounds of wandering feet.
My MIL takes 2 kinds of benzos--Ativan in the daytime, every 4-6 hrs and at whatever dose it requires to keep her from raging. Nighttime is a whopper dose of Xanax and she'll sleep for 14+ hrs.
Of course she says she never, ever sleeps, but enough nights spent with one of the kids in house and watching her, shows that she rarely gets up. Also, since she cannot remember how to attach her oxygen tubing to her CPAP, she gets kind of frantic when she has to reassemble the whole set up.
Without being on benzos, everyone would be miserable.
Situations are as individual as one's own finger print and they vary accordingly, so we would need much more information:
1. What do you mean by "caregiver". Is this a spouse caring for someone, a home help caregiver? a med tech in a nursing home/ALF/MC?
2. What specific sleep problems (or better said, lack of sleep problems) that the client is experiencing? Is this unable to sleep at all, wakefulness to go to bathroom, agitation, too much sleep during the day? Just exactly what is happening with the client?
3. Who is in charge of medications? MD and spouse/cargiving child, or medical tech in the facility?
4. What is the unwanted result?
Are there falls occurring in attempt to get OOB but too sleepy to do so?
Is there incontinence due to over medications?
Dependent on the situation and who is in charge (POA, spouse, child, person themselves?) will be the outcome in this situation. For instance:
You MAY have the case of an elder who has irratic sleep patterns, is up and roaming, and other spouse is caregiver/unable to get any rest?
You MAY have an elder in care you feel is being overmedicated to "keep the peace" at night?
You MAY have an MD ordering medications on a PRN basis ("as needed/requested") that is too strong and administered too often by staff; MD may be unaware of unwanted side effects.
Hope you can fill us in a bit, so we can try to help more.
Best to you.