He suddenly (for the last week) is more and more uncooperative. Refuses to listen to me and follow my suggestions. Today he refuses to wear the incontinence protection and refuses to get up. After lots of coaxing he finally took his medicine, now tells me I am from hell and to keep my mouth shut. Refused to let the care-givers we have coming in for 2 hrs twice a week touch him or help him with the toileting. How can I get him over this anxiety phase? How long will this last?
But don't let him get away with pushing you put him in his place
my husband CA.nt talk but he did a little of those bad thing you just have to be the boss no one likes being sick just give him some space when he yells walk out and don't come back till he calls you nice and hugs you and shows he was wrong
with this he had all his marbles and stopped he also took mood meds he's not doppey he's just relaxed but don't let him abuse you if he doesn't under stand you will. Need new ways to deal with it as well if no let him know he can't get away with bad behavior I'll or not get him to a concellor he may need to get some fun happiness out that he's been trying to deal with that he can't express to you
THEN most importantly get some cans and cut some more shoulder epaulettes, so that you are not taking the abuse personally, and can deflect it.
I know a lot of elderly get so sensitive that they cant wear their undies the usual way and have to have the seam out [ modern clothing, has improved] but it can be something that simple.
For daily things like getting out of bed.. don't give a choice, but say "I have your breakfast ready, so get up now and go to the bathroom and I shall see you in the dining room." or whatever, he might have forgotten what to do, so resists all.Then when their day triggers off the by rote memory they can improve.
"Istill hav eosme PTSD Fromt he six year."
I also find I need to recoover from the worst years with my mom. It was about five years of going from bad, to worse, to worst. And I have had thirteen months to "recover." I am noticing that it is easier to be around her and to not feel guilty when I am not, and also to see her as a "patient" and not a p.i.t.a.
"Recovery" didn't happen the minute she went into AL. Not by a long shot.
I am wondering if others have noticed a recovery period and how long it lasts/ed.
Once I knew he had dementia I determined to stay with him in sickness or in health. It took 6 years for him to move mostly out of this phase and become more calm and reasonable. Thank God! He still pulls some of the negative behaviors, but I've had counseling on how to react and cope and he's much, much better now for a year. I still have some PTSD from the 6 years. I had to set boundaries of places he couldn't enter to startle or disturb me.
There's hope that a person whose behavior is harmful to the caregiver can improve! Naturally my husband no longer believes he has dementia and chooses to forget he was diagnosed with it. He stopped his medication and would refuse to do anything about caring for himself in terms of his dementia.
SisterLisa,
Thank you for sharing that story. It really helps to have such confirmation. Some people believe that it is not right to "drug" elders into a correct frame of mind. But how can one argue that happiness is not better than misery?
I learned the hard way that memory loss/dementia causes anxiety and that anxiety eventually can lead to paranoia with a capital P. Things go along, go along, go along--and then they don't. That is the point at which you need the right medications. You have arrived.
My mom's family doctor it turns out, was not giving enough of the right stuff to have any impact. After about 18 months of her distrust and surliness, we sent her to a Senior Behavioral Center; there are many all over. She was there for ten days and they fine-tuned her medications. The result? She is a different person!!!!!!!!!!!!!! Calm, pleasant, and happy to see me whenever I arrive. I am so grateful to the scientists and doctors who made this possible. The bill? After insurance, only $1,000. Well worth the money!
Understand the possible causes and share them with your contacts at the local police community officer, family and friends.
I aggregate (collect these tidbits on
"Dave Mainwaring's Knowledge Network" )
Sunrise Syndrome,(sun?riz) a condition in which a person with Alzheimer's wakes up rising in the morning and their mind is filled with delusions which include include beliefs about theft, the patient's house not being their home, a spouse is an impostor, belief an intruder is in the house, abandonment, spousal and paranoia, people eavesdropping. Sometimes the person may carry over content of a dream.
One observation is that Sunrise Syndrome is different from Sundowning because the person may wake up in a confabulation mind set. During a Sunrise Syndrome conversation with the content may filled with confabulations; verbal statements and/or actions that inaccurately describe history, background and present situations.
Sundowning in contrast displays as confusion, disorientation, wandering, searching, escape behaviors, tapping or banging, vocalization, combativeness; the demons of anxiety, anger, fear, hallucinations and paranoia come out.
Hallucinations and delusions are symptoms of Alzheimer's disease and other dementias. With hallucinations or delusions, people do not experience things as they really are.
Delusions are false beliefs. Even if you give evidence about something to the person with dementia, she will not change her belief. For example, a person with dementia may have a delusion in which she believes someone else is living in her house when she actually lives alone. Delusions can also be experienced in the form of paranoid beliefs, or accusing others for things that have not happened. For example, the person with dementia may misplace an item and blame others for stealing it. Some people with dementia may have the delusion that others are "out to get them." For example, he may believe that his food is being poisoned.
To learn more about Alzheimer's/Dementia go to the blue bar near the top of the page.... click on SENIOR LIVING.... click on ALZHEIMER CARE... now scroll down to the various topics. Lot of good information there.
You might make sure he's not injured, sick or in pain. Sometimes they aren't able to communicate that and they act out instead. Does he have any rash or sore spots that are sensitive. Is the soap too strong. I'd rule those things out.
If it's not that, then it takes various attempts to get the cooperation. That requires lots of patience, time and effort. It may not ever get better as long as he is verbal and has the strength to protest.
My loved one is on Cymbalta and that helped tremendously with her agitation. She still sometimes needs encouragement to get out of bed and allow her baths, but it's much better with her on Cymbalta.
Sometimes the rapport they have with the person providing the care can sometimes play a part too. I think they sense people who are impatient, nervous or in a hurry. Has that changed lately?