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My husband of 25 years is having great difficulty with denial in regards to his advancing Parkinson's Disease and my increasing difficulty caring for him in our home.


I drew a final line in the sand this morning: He will need to move into a nursing home. I will need to visit him there every day. He does not believe that this is going to happen, likely because of mental changes due to PD but also because he has always been a denier.


I cannot, I will not change diapers on the man I love. Can't do it. Won't do it. He denies he has intermittent urinary incontinence, even in face of concrete evidence to the contrary.


Today, I told him that there were two ways we could get him into a nursing home.



  1. Call 911, get him taken to our local hospital, and then enter the nursing home.

  2. Plan to select and go into a nursing home for evaluation.


He chose option 2, although he believes that if we go for option 2, he can convince the nursing home that he is not a candidate. Given our health care system, he may be able to do just that.


I wanted option 1 because I believe I can get more assistance (e.g., social worker at hospital) than with a facility that might have a vested interest in either turning him away (the better ones) or a vested interest in taking him because they need clientele (the lesser ones).


Input please. I am posting this is another forum as well since I'm new to this site.

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You can no longer consider your LO as a partner in decisions. You have to do what makes the most sense, is the safest, and the healthiest for both of you. It is a hard act after working together for so long, but essential. Get used to it or you will get emotionally depleted. Think of it as if you were advising your sister or your friend. What would you tell them to do. The do that.
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Reply to RetiredBrain
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I took my mom for a visit at a facility and they know the symptoms - IF they are paying attention AND care. The person "interviewing" would ask a question, my mother would answer and I would shake my head or smile knowingly or say "we wear disposable underwear" and "we have found two on at the same time" - in other words truths that counter what the person is answering.
If the facility does NOT seem to understand, then you are in the wrong place or with the wrong interviewer.
Be confident in your answers. YOU know what it happening. YOU know what he will say and YOU have the truth. He says "I'm not incontinent" and you say to the staff member listening "that's why I clean soiled ... everyday" or whatever the specifics are. And get specific, not nuanced, don't hide ANYTHING "nasty". Be blunt with a loving, caring matter of fact tone.
As a daughter there are many items I did not think I would ever discuss with my parents or caregivers. At this point in my journey, nothing is off limits. Not potty stuff, not sexual stuff, not body irregularities, nothing. They aren't called "hard discussions" for nothing and the "hard" is on me, the cognitive person that handles the "everything" and has to talk to caregivers on a regular basis.
Be firm, loving and KNOW it is the right move for you. He will argue, deny, verbally abuse so you need to REALLY KNOW in your heart this is the right move AND keep knowing it through the junk. Safe your heart and your life.
Get your paperwork in order - DNR, POA, MPOA, trust, will, list of assets, etc. In Arizona, where my dad is (my mom passed last month) there is a Mental POA as well. I hope you have most of that in place already.
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Reply to RainbowHeart
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The denial is unlikely to change. It is often part of, and an indication of the disease.

Welcome and glad that you are here and that you have been honest with your husband.
Now do tell me that you are also his POA and that was done when he was competent. (This may be part of his will; a document called Spring POA) would allow your MD who treats his Parkinson's and one more MD, usually a neuro-psyc examiner) to write you in as POA.
You would then choose his plan of care after examination of his assets and yours with an Elder Law Attorney, and division of assets to protect your own money.
You would then examine placement. He may qualify for locked unit in inbetween care which is sort of an ALF with more staff and locked facility. Do the tours. Consider using A Place for Mom type businesses if he will enter self-pay.

Lots involved here. First is qualifying yourself to act and protecting assets. 2nd will be examination and diagnosis 3rd will be placement.
Wishing you so much good luck; hoping you have family or friends for support.
1. POA
2. Diagnosis
3. Choosing facility
After that he can be transported by medical van.
Good luck. Keep us updated if you will. Read up on the Forum; there's lots to learn here.
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Reply to AlvaDeer
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Option 3. Find a place on your own, get paperwork from the facility, take him to his doctor and ask for paperwork to be filled out, then bring him to the place. Marketers can be very helpful on creating the story line and you already have the ruse. Tell him you are taking him to see a place and that they are offering free lunch. ( most do). Leave at the appropriate moment.
When you visit places, this is where you mention his reluctance.
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Reply to MACinCT
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"Given our health care system, he may be able to do just that."

Please understand the differences of facilities that take care of our loved ones. Someone has posted about that. Facilities have evolved in this modern age to meet the needs of the residents they serve. Their caregivers are better trained than ever, attend training sessions as part of their jobs, and are kind, caring and wise. They wouldn't last long in those difficult jobs if they weren't.

I'm not a caregiving professional and have never worked in the medical field, but I've had lots of experience in placing loved ones and in caring for them at home. I have no vested interest in speaking up for care facilities, but I believe that they are sometimes needlessly maligned and that standard beliefs about them are often wrong.

Please don't underestimate them. Facilities handle things in a very professional manner in most cases, and your husband most likely will not be able to put anything over on them. He will be evaluated by professionals who are accustomed to anything he can throw at them, and he will be placed according to his needs. Our health system is much better than you're giving them credit for. My husband currently resides in memory care, his second one in the past 6 months. Both places are doing their very best, and he is content.

Why in the world would any facility have a vested interest in turning anyone away? They need to make money. And how would you know the difference between a good place and a bad one? Visit some. Then you'll have a more accurate picture of "our health care system."
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Reply to Fawnby
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TouchMatters Mar 2, 2025
It depends on the facility re level of care.
I presume some that charge $5,000-$10,000 a month, they have top of the line trained personnel. However, nursing homes for those who depend on government aid is quite different.

Ultimately, a person moving in or having a loved one move in needs to do their due diligence, ask a lot of questions, take a tour, meet the staff, read the contract.
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So sorry you are dealing with this, it is very hard generally. Harder when the LO is in denial or impaired to the point they have no real awareness of the situation. Hang in there, hugs.

If you do not have an elder care attorney licensed in your state, I would highly recommend getting one on board asap. Depending on how your "paper work" is executed; there may be things to do or not do and depending on your State law (each state law is different, re: things such as a POA, guardianship, finding the person lacks capacity to make decisions thereby allowing you to take over).

Further, the paperwork from a nursing home (AL or other facilities) is a contract! You'll want an attorney to review as there are "trick questions" in these contracts, such as you agree to take him back if funds run out or he's a "problem" resident. Those words "problem resident" are not in the contract, but tricky legalese can be confusing by intention.

You want the facility to have the responsibility of a "safe placement" if he cannot stay in the facility you choose. If you agree to take him back, they just dump him back in your lap to work it out.

These facilities are expensive, and an attorney can help work through ways to protect you financially as the spouse not in need of nursing home care.

Contact you State Bar Association for names of licensed elder care attorneys where you live.

Also, they will know the best facilities to consider!

Good luck with this
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Reply to Sohenc
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Feel for you, facing same issue with spouse soon. Anosognosia can be total, other-worldly, denial. Even medical personnel don't necessarily 'get it'.

When you have time, read Contented Dementia by Oliver James. One tip from that book, for Move-In day (to the home): Have a family member or friend already there before he gets there, then have that friend/family member 'accidentally' stumble on husband and sit down for a chat. As if he/she also lives there. Also, if the gambit is that it is a 'temporary' stay, don't make his room look like home, initially, but keep it sparce as if it were just a hotel room.
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Reply to EddyJC
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Not alone. My aunt is in serious denial of her dementia and her incontinence.
She will scream and holler and go on on about not having dementia.
She had a real fit when I first visited and stayed at her neighbor's home until the house was cleaned and sanitized. She took it as her home not being good enough for me, when in fact that wasn't it at all. She messed all over the house and beds and expected me to sleep in it. She thought it wasn't "tidy" enough because of papers lying around, clothes not folded and dishes in the sink. That wasn't even it at all. I had it professionally cleaned, but am sure it's right back to how it was before and I refuse to spend a penny more of my money to have it professionally cleaned and sanitized.
Be happy you're getting him in a facility. I envy all of you who have made this commitment. It's best for all involved.
I would go with option 2, because 911 failed me. If he changes his mind and not go, then try option 1, although it didn't work for me. All the best.
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Reply to Tiredniece23
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You have gotten some great advice above. First, let me address my pet peeve: (as a former professional and as a family member who has had daily care for five individuals with cognitive impairment) denial is a psychology description that on some level involves choices. Our loved ones have lost the ability to choose - as in considering all factors, comparing possible outcomes, and making rational decisions (not that all my decisions have followed the entire process). The part of the brain responsible for that I is one of the first damaged by the process. Why do I think remembering this is so important? Number one: it helps me with the minute to minute battle to avoid taking things personally. They are no more talking sense than the three year old yelling “I hate you” when I don’t give in to an unsafe request. Number two it helps me remember I have to be the decision maker and not argue, just take needed action (not my nature). Number three it helps me remember my dignity and theirs. In all cases with my loved ones, placement started w/ their doctor (who, by the way gave me a referral to a social worker when I asked about it). I can’t agree more about the elder attorney. Finally I wish you strength and support with this difficult process.
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Reply to GrandmaKay
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Take him to ER to evaluate his incontinence issues. Let them admit him and help you with placement.
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Reply to Taarna
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