By proceeding, I agree that I understand the following disclosures:
I. How We Work in Washington. Based on your preferences, we provide you with information about one or more of our contracted senior living providers ("Participating Communities") and provide your Senior Living Care Information to Participating Communities. The Participating Communities may contact you directly regarding their services. APFM does not endorse or recommend any provider. It is your sole responsibility to select the appropriate care for yourself or your loved one. We work with both you and the Participating Communities in your search. We do not permit our Advisors to have an ownership interest in Participating Communities.
II. How We Are Paid. We do not charge you any fee – we are paid by the Participating Communities. Some Participating Communities pay us a percentage of the first month's standard rate for the rent and care services you select. We invoice these fees after the senior moves in.
III. When We Tour. APFM tours certain Participating Communities in Washington (typically more in metropolitan areas than in rural areas.) During the 12 month period prior to December 31, 2017, we toured 86.2% of Participating Communities with capacity for 20 or more residents.
IV. No Obligation or Commitment. You have no obligation to use or to continue to use our services. Because you pay no fee to us, you will never need to ask for a refund.
V. Complaints. Please contact our Family Feedback Line at (866) 584-7340 or
[email protected] to report any complaint. Consumers have many avenues to address a dispute with any referral service company, including the right to file a complaint with the Attorney General's office at: Consumer Protection Division, 800 5th Avenue, Ste. 2000, Seattle, 98104 or 800-551-4636.
VI. No Waiver of Your Rights. APFM does not (and may not) require or even ask consumers seeking senior housing or care services in Washington State to sign waivers of liability for losses of personal property or injury or to sign waivers of any rights established under law.I agree that: A.I authorize A Place For Mom ("APFM") to collect certain personal and contact detail information, as well as relevant health care information about me or from me about the senior family member or relative I am assisting ("Senior Living Care Information"). B.APFM may provide information to me electronically. My electronic signature on agreements and documents has the same effect as if I signed them in ink. C.APFM may send all communications to me electronically via e-mail or by access to an APFM web site. D.If I want a paper copy, I can print a copy of the Disclosures or download the Disclosures for my records. E.This E-Sign Acknowledgement and Authorization applies to these Disclosures and all future Disclosures related to APFM's services, unless I revoke my authorization. You may revoke this authorization in writing at any time (except where we have already disclosed information before receiving your revocation.) This authorization will expire after one year. F.You consent to APFM's reaching out to you using a phone system than can auto-dial numbers (we miss rotary phones, too!), but this consent is not required to use our service.
*If I am consenting on behalf of someone else, I have the proper authorization to do so. By clicking Get My Results, you agree to our
Privacy Policy. You also consent to receive calls and texts, which may be autodialed, from us and our customer communities. Your consent is not a condition to using our service. Please visit our
Terms of Use. for information about our privacy practices.
You can try, and I mean try, to meet them at their level, but after awhile, you crave the company of sane people to be around. Some of these people can be impossible to deal with, and no amount of redirecting or any other techniques would work when a seniors gets stuck in a loop. Sometimes family members are in denial about their loved ones and this person may need a higher level of care beyond home care.
There is nothing worse than harassing an overworked, underpaid aide doing a thankless job for these seniors. Our time and energy is stretched to the max and sometimes to the point of ignoring our own families and health needs to attend to others.
Aides get blamed for everything by seniors and sometimes well meaning family members. This is the worst of the worst I'm describing. Aides can only do but so much, and once a senior gets in their mind to target an aide or a certain family member, that's it. You may want to try another aide or that particular family member can pass the baton to another caregiver.
However, we have to greet these folks with smiling faces and a willing spirit of helping.
Aides keep up front that being dismissed from an assignment has nothing to do with our abilities to care for people with dementia, but a senior or family having a certain preference of another aide or family member, and that's okay.
Meet them where they're at. I had a client who sometimes believed that her parents were there with her, sometimes her brother, or "the kids" I would comment about their welfare and follow up with distract and refocus.
If she was focused on her Things we could discuss the items. No shame or guilt attached as her brain probably doesn't understand those things. But she will definately pick on the emotions attached to those.
Below are two excerpts from my book "Dementia Care Companion"
Accusing Others of Theft
The patient may stash away items or give items away, and forgetting that they have done so, accuse others of stealing. They may gift a scarf to a relative, and upon seeing her wearing it a few days later, may accuse the recipient of theft and demand the scarf be returned. This behavior is common in dementia and a source of consternation by those who are unaware of the illness and the resulting behavior changes.
· When the patient misplaces an item and accuses someone of theft, do not confirm or deny the alleged theft. You cannot convince them that they are mistaken. Instead, help them find the missing item.
· When the patient demands the return of an item, such as a gifted scarf, return it. Alternatively, avoid the problem by never wearing the item in the presence of the patient.
Hoarding
Hoarding is most commonly seen in Alzheimer’s disease, frontotemporal dementia, and Lewy body dementia. Around 23 percent of dementia patients develop hoarding behavior, typically in the early and middle stages of their illness.
Patients hoard all kinds of stuff. They collect, organize, fold and package them, put them away in nooks and crannies, and then spend many busy hours searching in various drawers, cabinets, and wardrobes to rediscover and unpack the items, only to repackage and store them again.
Hoarding typically occurs in tandem with obsessive-compulsive behavior, overeating, and pilfering. What all these behaviors have in common is an underlying sense of anxiety, impairment in impulse control, and memory loss. The patient is trying to get a grip on a life that is increasingly out of their control, with a mind that is no longer able to hold on.
Hoarding is also seen in some older individuals who do not have dementia. Hoarding in older individuals may be a precursor to dementia and a warning sign.
How to Handle Hoarding
Although hoarding can be challenging for the caregiver, it does not help to get angry or scold the patient. Patience, creativity, and humor are better ways of handling all kinds of behavioral problems, and hoarding is no exception.
· Find out what drives the hoarding behavior and try to remove the cause. Is the patient worried that their stuff may get lost or stolen? When they spread, repackage, and store items, are they trying to reassure themselves that they can find the items again? Are they bored from inactivity and a lack of meaningful involvement with the daily household affairs?
· What do they collect and where do they store them? Are the collected items perishable? Are they valuable? By knowing the types of items that the patient likes to collect and where they stash them, you can better decide your next steps.
· Reduce the number of drawers and wardrobes that the patient uses. Label drawers to clearly show what’s inside. You can write “socks,” “underwear,” etc. on sticky notes, then attach the notes to drawers. Or, you can affix pictures to drawers, indicating their contents.
· Make life easy for the patient. Use a large plastic basket for the collected items so the patient can easily find them in one place and pack them again when finished.
· If a particular type of hoarding does not pose a hazard, let it be. But, if the hoarding creates risks, such as food that spoils or clutter that presents a fall hazard, find ways to remove the risk.
· Avoid removing or discarding hoarded items as this may add to the patient’s anxiety. Find other ways to remove any risks. For example, if hoarded food has spoiled, replace it with fresh food.
· The patient may agree to donate some of the items to charity. Take this opportunity to quickly
maybe take pictures of the room and stuff / or keep record of how many stuff are there?
some aides do take things I imagine so Not an altogether dismissal
If funds allow maybe put up a camera
Or a cabinet with lock on it and pack stuff away in it
you keep key?
good luck
I agree a low dose of Ativan to calm mom down is a good idea.
Also, give her a big box of things she can rummage thru to her hearts content. Rummaging can offer a measure of comfort for individuals with dementia, offering recognition of familiar objects and a way to find purpose and meaning.
Giving mom some small job like folding towels or sorting spools of thread may help her as well.
Good luck to you.
So often did this happen with my partner's mother, accusing her long serving Wilma over and over of this and that, that now when either partner or I lose something we always giggle and say "Wilma took it".
There is no reasoning, and there is no argument with a disease like this. Simply express your sympathy with her and attempt to move on. When obsessive thinking and acting out becomes continuous speak with doctor about some try at low dose anti depressant. That can sometimes help a bit. But often doesn't.
At some point you will be left with choices about how long you can continue home care with someone who really needs several shifts of several people each to deal with the continuous problems this condition brings.
Good luck.
Have you tried taking pictures of her things, so that when she thinks something is missing you can show her the pictures to reassure her that they're still there?
That may or may not work, but the important thing for you to remember(since your brain isn't broken)is that your mom can't help what she says or does, and that things will only get worse as her dementia worsens.
So if her care is getting to be too much for you then it may be time to think about placing her in a memory care facility where you can get back to just being her daughter and advocate and not her stressed out caregiver.