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.
Accordingly, there is no choice for her to make.
My mom is in assisted living and her dementia has just exploded because of covid19.i can sit on the porch with her and thats it, because i cant come in and visit with her shes gotten stir crazy, always telling me she wants to go home.i recently tried to move her to a different facility, id previously showed her pictures explaining the facility to her, she was totally for it. When i got her there, she was totally confused, acting like a deer in headlights and absolutley refused to stay.
I get the tough love thing, but you have to know they're really ok. If a parent cant remember certain things, they at least deserve to know they are loved.
By you explaining things to her is a respect thing, how i see it.
Dealing with a loved one that has dementia and changes gears every time you talk is a really difficult thing, just making a decision for them, ive seen with my mom, can leave them worse off being left confused i dont know if anything I've said here is helpful, but my heart truly goes out to you, and if you ever need to talk or vent, plz shoot me a message. isnt that what this website is for?
The support?
Best of luck to you, I'll definitely pray for you,
Move her to a memory care place.
Once in her new home, she was confused, and shortly after, was diagnosed with dementia, which we kids all knew. That diagnosis was very distressing to her, as her mom died of Alzheimer’s and my mom was terrified of having Alzheimer’s. So we now refer to it as CRS, “Can’t Remember Sh*t”, which seems to be ok with her.
My point in all this is, even though bottom line you are having to step in and play the adult role, doing what is best for your MIL, there are ways to lighten up the process, being firm (about the decision), yet gentle (about how you make it happen). Good luck to you!
When it came time for me to make this decision, I just did it. I had to have a hard heart and do the job. Got paperwork, got doctor's exam, signatures, already had the health care directive for my husband's wishes, in hand, made all the arrangements and drove him there. Don't you think after 58 years with only one year apart, when he was in Vietnam, and for 57 years, lying in bed with him and waking up to a caress and kiss, that I wasn't wrenching my gut that this was wrong, sick of me not to care, regretting getting papers signed, lining up the movers to deliver his bed, favorite chair, favorite painting, favorite family pictures, a good bit of his clothes, and walking him to his room? It was the right thing to do. But, lucky for me, that my husband didn't disagree, he didn't know any better by this time, he just was a danger to himself by leaving the house, and you've heard this from me before, crossing 6-lane boulevard on a Sunday afternoon when there was barely traffic. Don't you think my heart bled that I had to face facts, he wasn't getting better? My sister and brother had this problem with my Mom; she and her husband had their own apartment, thought she didn't need assisted living, drove my sister crazy with bank statements, called my sister a thief, when there was no such stealing from my Mom; called the manager a thief for stealing her load of sweaters my sister gave her, only to be in her drawer where she put them. When the time came, my brother drove from Delaware to pick up my Mom and step dad, drive them all the way to Delaware. On the way there my brother had already arranged for their room in assisted living, and he brought them there, all while, telling them during 6 hour trip, he wasn't taking them to a home. But he did, for their sake and safety. Oh, yeah, my Mom was blazing mad, using every cuss word she could think. Slapped my brother and tried more, that she was p___ed off, she hated him, didn't want to see him. He had to have tough love, as he saw how my mom was keeping house, her husband making a sandwich and eating it with molded cheese and meat. That was the little clue. My brother stayed away the required time, as I did with my husband. My Mom fought like hell, but she was safer than her own apartment. My family wished they had done it sooner. I was not living in the country so could not leave my job overseas and help. I only agreed with what they did. Sometimes grown children of demented parents have to have TOUGH LOVE. For the safety of their loved ones, no matter what they said about not ever wanting to go to a nursing home, wanting to stay in their home, have tough love and take care of what has to be done--for your sake as well as theirs, just get it done.
You just keep moving forward; this is a good plan. It does not matter if she is mean to SIL; she has dementia and maybe is mean all the time. My mother is mean; so what, I know she has a broken brain and I don't get offended or upset.
You are overthinking it now. You have the plan; just decide how she will get up to NJ and do it. My mother did not want to move; she thought we should take care of her at home. We had MD report stating she could not live alone so we blamed the doctor and placed her. And just so you know, when she was placed, she was happy for about 2 hours and then she started calling for us to come and get her out. That lasted for 2 weeks.
For now, baby steps, just get her in there. Good luck; this is no fun.
I did want to mention she is moving into independent living within the facility, she is capable of daily life skills for the most part. During Covid we thought this best since IL can come and go and we can do things with her outside of the facility. Right now AS and MC is on lockdown.
wish us luck on Monday when we attempt to bring her back to NJ!
So the only way we got mom on board, was to say she could try it for 2 weeks, then she could give 30 days notice if she didnt like it, and she would only be out a month rent and a small administrative fee. She said she just wanted a few things moved, I think she finally said ok, so we would shut up about it and she could point out she tried.
Since then her dementia increased and shes had to move to Memory Care. One thing that we did is that they allowed her to do 2 covid tests, one 48 hrs prior, then one day of move in. She got results next day for both of them, negative so she did not have to be quarantined when she moved in.
If HER SAFETY, SIL’s wellbeing, YOUR HUSBAND’s ability to provide the best circumstances FOR ALL OF YOU, FOCUS ON DOING WHAT MUST BE DONE.
Whether she is “mean and accusatory” or not has NOTHING to do with doing the best you can for everyone involved.
NO ONE in your situation will be completely happy with how this goes down, but at this stage of her care, compromise among less than good situations becomes the best you can do. If her cognitive assessment reveals anxiety/depression, a small dose of carefully chosen mood stabilizing medication may help, and it’s worth a try.
You have all thought this out kindly and fairly. If the assessment of her cognitive functioning does not reveal that she is not safely living in her present setting, that time will occur soon. You all know that dementia is progressive. There is no strict time line of course, but also no question that it is irreversible.
If she qualifies for Memory Care it will most likely be the safest, considering your concerns about her potential attempt to leave. The residence you are working with will typically help with that decision, but with Covid 19, many no longer have the luxury of too much mutual decision making.
Choose the simplest method of getting her out of her current situation, ignore the hostility, rage, threats, ignore “changes her mind”, bring small familiar possessions that will make her feel more at home in her new setting and move larger pieces when she’s settled and you have a little time to make those kinds of decisions.
Although this feels as though you’re all alone in this, her pattern is tragically familiar to many (probably most) of us. Hope you are able to make some sound decisions, combining love and safety to come up for what is best for her.AND FOR ALL OF YOU.
Break for SIL. Temporary stay with you. Medical look over coming up.
Yoir MIL is in good physical health & with such a lovely supportive family has the best chance to transision to an AL where she will be a bit safer going forward. To do this before the memory issues get worse is your best ally. Good job! 😊
- does hubs have DPOA & MPOA that is legal for NJ law?
- does MIL have significant assets to pay on her own totally for AL for 3-4 years? Say 200k-300k available between her existing savings & her monthly income (like her SS $) over time?
- if not, is her $ interdependent on her selling her home.? & if so, what realistically could sale bring in deducting $ to make it market ready, Realtor & Act of Sale costs? Is SIL owed $ from mom for paying for house stuff over the years? Or you & hubs owed $ from mom? Like maybe family paid her tax assessor bill.
If she still has her home, is anyone expecting to have it given to them? Or lives there right now?
- if AL doesn’t work out, does she have $$$ for MC or NH? Or will you & hubs pay her costs to stay in NJ? Even if it should be that she actually needs skilled care @ $8-12k mo? Wherever she is, will, I’ll bet a case of a Prosecco, want y’all signing off on some sort of financial responsibility agreement as she has no well established history as NJ resident (so not easily onto NJ LTC Medicaid should stuff go awry should you have her in a facility that even takes Medicaid).
- are you assuming Medicaid (not MediCARE) will be covering her costs on NJ? Not perhaps Initially but eventually she will need MedicAID.
- has she had a “needs assessment” done? If not, please get one done ASAP. You do not, again DO NOT, want the new AL saying “we just so love your mom but she needs a higher level of care & here’s your notice to move her out within 30 days”. Happens all the time. Needs assessment is not a note from her MD saying she needs AL. It’s a 1-on-1 done usually by a geriatric RN & SW team at her home. Personally I’d be wary of any facility who blithely tells you she can move in without a faxing & review of her current last 6 mo of medical records AND some sort of last 30 days evaluation in advance...... whether it’s a 1/2 day “play date with lunch & activity” at the place or a needs assessment; aNd all of these done before the place accepts her as a resident. She’s coming in from living at home, if SIL & her family have been doing oodles of stuff that enables her to live at home now for 14 years of caregiving, it may be that MIL is not at all suitable to be AL resident. Needing help pulling up a zipper or transitioning in & out of the shower might be ok for AL. But She’s going to be expected to get cleaned up, dressed appropriately, take her meds & over to dining & activities on her own for the most part.
Did you spend better part of a day at this AL & can your mom on her own do what the other residents easily do???
- what’s her health like? Does she have diabetes or other chronic diseases? Have you set up a whole new group of NJ MDs for her? In new AL, is she expected to be able to go see her docs on her own, and do her daily RXs? if she needs help with these then she’s probably going to be billed as a seperate fee for medication management & for an aide to accompany her & transportation costs. Unless this is an $$$ AL with concierge medical, all these are added on costs for AL & remain a mystery till she’s actually a resident.
- will her current health insurance transfer to NJ? Original Medicare does but the supplemental secondary to her Original may not; if she’s on Medicare Advantage plan, those don’t as they are tied into provider network for her section of NC. So what have you set up for her health insurance?
Physically moving her, I’d suggest that you move her via a large SUV tag team driving so no overnite hotel stop, the smallest possible clothing & personal items for basically a dorm size room. “Belongings” need to be jettisoned, 86’d, Goodwilled. Maybe take chest of drawers, bookcase & lamps. Maybe box up & ship soft goods. A lot depends on facility allowing outside furnishings.
why not stay in NC?
She has been living independently with assistance in purchasing her food. SIL brings her groceries weekly. She can takes care of her personal hygiene needs, can dress herself etc. all her bills are paid electronically, and so am on her account to make sure all bills are paid.
she is in great health, 88 years old and no medical issues no medication nothing!
we all feel bringing her to NJ is a necessity, she grew up in NJ and has lived there most of her life.
her health insurance is through NJ educators, that is not a concern.
as for $$ she will self pay with with her assets, then the sale of her home...we figure 7 yrs.
we have HCPOA.
the place we are going to is a 3 phase place with independent living, which is where she will start because she is able to take care of her needs for the most part.
it is so hard to explain, but bottom line is she needs to come back to NJ.
we have a plan, she will come for a visit while SIL is on vacation and then take it from there
You could suggest that as SIL is going on holiday, MIL will need to stay there a month - just for starters? Thank her for doing this to help SIL & you.
I know people will diss me for fibbing & I would try honesty first, but I have seen so many families struggle & struggle with this. I think it really comes down to the elder's personality & if they are willing to accept change or not.
How I reconcile it is although it's never nice to move people out of their home against their wishes - the effects of neglect leaving them unsafe at home can be worse.
Best of luck to your family through this transition.
It depends on how far her Dementia has progressed whether she needs to be in an AL or Memory care. Some are not progressed enough for MC. The AL u choose will evaluate Mom to see if they r the right fit.
But some other dementia types have faster progressions & may need more support sooner rather than later. Esp if other medical or mobility issues.
It is a continuum care place ie AL with NH & MC?
With the "formal" diagnosis there would not be a problem getting her into a facility particularly if the doctor states she needs 24/7 care.
I would caution you though that AL might not be the best place.
AL she can leave and go on an outing without supervision. She could sign out and go for a walk and not return.
Memory Care would be a better option. She could not leave without you or some other family member or facility staff.
If you do place her in AL as she declines she will have to move to MC and moves typically result in a decline shortly after.