My Mom has dementia and in a Memory Care unit with about 18 others. The unit recently introduced a patient who has outbursts all the time and bangs the table/floors, screams at other patients and I witnessed her hit another patient. She is stealing the peace of the others. When does the welfare of the others outweigh the needs of this one? They all get agitated. Shouldn’t there be other units where people are cared for based on their level of behavior. It seems very wrong. While I am sympathetic for that woman and her family, I’m concerned about my Mom and the others who don’t have a voice to change this. This is hard on the aides/staff also. I’ve brought this to management’s attention. Has any one else dealt with this?
It has taken years to interpret involuntary signs.
I feel bad for the times that I though my wife was just being difficult. Chrsity has FTD and cannot comprehend or communicate.
My nephew was born with CDL and also cannot comprehend or communicate.
He is now age 50
The FTD and CDL are not related.. It puzzles me that they both exhibit the same aggression, violence, difficulty when they are hurting. They both have almost insatiable appetites
Also of interest is their grumpiness is the same when there is a weather front.
They could be constipated, have a UTI, have to pee, even if they just did, feel a little nausea or heartburn, drymouth, joint ache, or an irritating itch that they don't know how to scratch. POLYESTER!
Christy has been a sweetheart since 2014, because we are constantly and immediately attentive to any possible discomforts.
Constipation and burning diarrhea are the most common.
Please be certain that the dementia is not FTD.
FTD reponds adversely to drugs, especially sleep medications.
Your doctors may not have the clinical expertise to recognize and diagnosis FTD.
It took them 9 years to recognize Christy.
https://memory.ucsf.edu/medications-dementia
What is the policy where your mother lives?
Sometimes there is a adjustment period for new residents and moving for a Dementia patient can be extremely frightening for them. Outburst are to be expected. That being said, safety for others should be put into place.
Go back to the administrators and ask for them to send the violent one to a hospital to find the right meds so she can get stable before she is returned.
If that doesn't work, contact the state board that regulates those type of facilities and send in your complaint along with a copy of all your documentation.
Difficult as it is, try to give this new resident time to calm down. Meanwhile, if possible, keep your mother's door closed and introduce sound - even white noise - into her room if possible to mask the sounds of others. I wish you luck.
You see what happens but you do not know what is being done for this patient.
And HIPPA laws prevent them from telling you what is being done.
*They may be trying to have this person's medication adjusted. This can take a while.
*This person may have been just been uprooted from the home they have known for years and is ..angry...scared...lost...
*Taking things from another person's room is VERY common and if you read many of the posts others have asked about it. There is not much that can be done.
*The administration may be having discussions with the family that the behavior is unacceptable and they may have been given some time for adjustment and if the patient/resident does not adjust they will be asked to find another facility.
Continue to monitor what is going on.
I would also send a letter, not an email, that you are concerned about your Mom's safety. If you have or if your Mom has a lawyer that handles her affairs a copy to the lawyer might be a good idea. You might even ask, since you are concerned about your Mom's safety and theft, if you can put a camera in her room to monitor her safety and her possessions.
And yes there are facilities that will take agitated patients/residents but I am sure this persons family is trying what they can to avoid that. There are forms of dementia (LBD) that the person can have more violent tendencies and it is a matter of medication adjustment. But like with all medications for Mental Illness it can take time to find the right medication, the right dose.
Continue to have meetings with the administration but Please be patient..
And yes, patience is the big challenge.
What was the management's response to your concern?
They are no allowed to physically or chemically restrain, but they rely on a rule that states unless then behaviors interfere with the others.
We have kept Christy home and we are happy. There are HBC programs and it is Congress intent that we do all possible to keep her out of a facility
.
See Olmstead
https://www.hhs.gov/civil-rights/for-individuals/special-topics/community-living-and-olmstead/index.html
Dementia does not meet the requirements for psych facilities or any psyche services as there is no medication, no improvement, no recovery, no means of testing.
Alzheimer's medication do not work and they have severe adverse side affects.
It really isn't fair that one person disrupts a whole facility. Not fair to that person and doesn't help when trying to keep anxiety low with the other residents.
You can always speak with an attorney if you feel the facility is not handling this the right way, but chances are that they are doing all they can. And remember, if you do speak with the facility’s administrators, there is only so much about this woman that they can divulge.
Moves are very hard on those with dementia.