My husband's family has a history of dementia. His grandmother, a great-aunt, and an uncle all had it and his mother just moved into full-time dementia care after 3 years of home care. For his mother and grandmother the dementia appeared very late, in their 90s. I am not sure about the onset for the other two family members except that the uncle's onset was much earlier. My husband and I are in our 50s and we've known each other for 20 years. He is fit and healthy with no addiction concerns.
He's never been good with time, not knowing if something happened a couple months ago or a couple years ago. We have started bumping heads over his lying about me (just to me, not to other people). There are 3 instances I can point to.
He is lactose intolerant. He drinks dairy-substitutes and I keep lactose-free milk for myself so I can use it cooking for him. I am not and have never been lactose intolerant. Occasionally he'll suggest I have a Lact-Aid pill with food, since it might have milk. He is convinced that I am occasionally bothered by dairy and that I have told him that before. I have never, never said that and I have no problem with dairy. He says I've told him before that I am bothered by dairy and often gets upset with me that I am always changing what I tell him I like and dislike from day to day. It is also one of the few instances where I can say with 100% certainty that I have never claimed to be sensitive to dairy. Other similar arguments on different topics have been making me question myself.
A few days ago he was making us dinner and was very angry with me about one of the potatoes being rotten. He accused me of putting a rotten potato in with the good potatoes to ruin them. I questioned his accusation and he said that it was "just like me" to do something like that. I got very angry and told him in no uncertain terms that I did no such thing. I don't even know where I was supposed to have gotten a rotten potato from! Later that evening he did apologize, which is extremely rare for him to do, but I was angrier than he's seen me since the cell phone problem below.
The worst and one of the earliest issues that scared me needs a bit of history first. He hates cell-phones, and we did not own one until about 4 years ago. I finally got one as a gift from my sister, but before I got it, he and I talked and agreed that we didn't want his family to know we had one because he didn't want them to be able to call while we were away from home. Especially his mom, who was not showing signs of dementia yet, but has always been quite clingy. I agreed completely with not sharing with them that I had a cell phone since I didn't want to have to field phone calls from them (we've always agreed that I "do" my family and he "does" his). About a year later, we had a big argument (we don't argue often). In the end he accused me of spending an entire visit at his mother's "playing on my cell phone". The problem is, whenever we'd been at her house it was on "do not disturb" and hidden in my purse. There was never a chance for her to ever see it or hear it or even suspect it existed. I never took it out of my purse while we were there. I know he's opposed to cell phones in general so I never "play" on it around him at all and keep it on silent when he's around. I have no idea where that came from or why he'd say such a thing. It was as outlandish and unrealistic as saying I ran in and punched his mother in the nose!
I really don't know what to think or what to do. I am hurt, scared, and frustrated at the entirely false and unrealistic accusations from him and I'm worried that they are increasing in frequency.
Many have suggested this is dementia. Giving a name to the symptoms (confabulation) is fine, but what is needed is to know what the cause underlying this confabulation is. Clearly there IS something, but we would all be remiss in not directing you to get medical help.
We can guess, give examples and confirm all we want, but there are MANY conditions which can mimic the symptoms of dementia. What you should aim for is a THOROUGH exam, which may include referrals to specialists, to rule out any other cause before assuming dementia.
One time on my way to work, I called my mother. She was in a very confused and unhappy state, so I stopped there first. We ended up at the ER and then admitted, as her potassium (and likely other) levels were too low. In her case, she was drinking too MANY fluids. Once restored, she returned to her usual nasty self!
I understand you currently don't have a doctor and have limited choices. Perhaps you could start with your insurance company - often they have listing of those who honor your plan AND are accepting new patients. Document all these issues so that you can present them to the doctor. He may resist going, insisting he is healthy and doesn't need to go. Try to work around that, perhaps by saying the insurance requires a recent checkup. Make appt for yourself as well, so you can "support" the claim that everyone needs to do this.
This link has a brief overview of confabulation, lists SOME potential causes and has suggestions for how to respond to the "stories" or beliefs of those who are beleaguered by them.
https://www.verywellhealth.com/responding-to-confabulation-in-dementia-97969
This link is just FYI.
A thorough exam, including bloodwork AND urine test (UTIs can cause so many bizarre symptoms in people!) If all seems to be in order, the doctor should include tests like MRIs and potential follow up with specialists. Not all doctors are worth the paper their degrees are printed on - if you don't feel comfortable with the one you see, find another! If the doctor dismisses your concerns, find another! Even if you have to go some distance to find the right doc, do it.
While I certainly wouldn't assume he has any form of dementia, it is a possibility. Getting to the bottom of his odd behavior is important (not all types of dementia are hereditary. None of mom's or dad's siblings had dementia. I know of no one in extended family who had any form of dementia. She is the only one left now of her generation and developed this when over 90, so most likely her case is vascular, because she has high BP (has taken meds for YEARS!) IF they can get to the bottom of his odd behavior, it will at the very least be a little relief, but make sure you learn all you can about whatever the cause is, esp if they don't provide any info or point you to where to get assistance.
Hoping for both of you that this is NOT dementia and might be something that is fully treatable! Meanwhile, go with the flow when he makes these outrageous statements. Stay as calm as you can. It isn't worth fighting about it and it won't help at all!
I am sure you can come up with a "good reason" for you both to go to the doctor so that he can be evaluated.
Take care.
I know.. It's not about those things.. Something will always come up,... If it isn't one thing, ie. potato, it's another.
gotta point a finger some where, right?
lynina2 is is p;onting in the right direction..
i knew there was something wrong when h misunderstood and misconstrued visits and conversations with me and others. I believe This is the emotion part of VaD. He NEVER misunderstood anything to the good or positive, it was always negative misunderstandings, you can’t argue with them b/c this is how dementia works.
I was never able to make him understand Th is was abnormal and not like him. Then a year later he would cry or laugh inappropriately. Then he could not find words to express himself.
I guess you need to be able convince him he is not acting like himself and get a neurologist eval. I’m so sorry.
I was devastatingly hurt by my mother for whom I was the primary caregiver a couple of years ago. She accused me of all kinds of things that she said that I said and did. Then she told my three (3) younger siblings who were basically estranged from her stories and they hired lawyers against me. It’s been an absolutely horrible last five (5) years because of what they did to me.
I would recommend that you have him tested for dementia and Alzheimer’s as well as tumors in the brain as soon as possible provided he cooperates. (My mother refused to have any testing done and was a narcissist which really multiplied the problem.). Best of luck to you and try not to be hard on yourself because it isn’t you where the problem exists.
I'm not being (just!) nosey; what you describe could be a layer of personality emerging, or it could be something new and sinister - or it could be something new and eminently treatable, of course, let's not get ahead of ourselves.
You say he's never been good with time. Are there any other related quirks that you've always known about?
Don't think of it as lying, don't think of these as accusations. They are distortions in his recollection, they may irritate him which leads him to pick on you as the (wrong) source of the irritation.
What did the argument about the cell phone that you never look up from 🙄 begin by being about?
These are also signs that due to Covid, people have been locked up together at home for far too long. imo.
The rotten potatoes, the cell phone, the lactose intolerance---,
someone must have been reading my story. A bot maybe.
Some details are different, but my husband has had significant similarities, and it is hard to understand or deal with it.
That is why Lymie's advice was invaluable to me. I have to go in the other room before I 'fly off the handle'. It hurts so much to have him falsely accuse me, to doubt my support of him.
Cell phone:
He bought an android cell phone 3 years ago, unlocked. Has never used it, hoarded it while I went without. Where did he get $300, he says I knew about it. I did not. It is too old now, a '5'.
And Pronker! I am going to need to try these techniques you offered:
"We want to defend our honor by saying, "I did not do X," and that's the most difficult issue to scale back for me. A list of noncommittal answers helps: "How about that?" "Who would have guessed?" "Huh, no kidding." etc. and then I go Gray Rock. Please look up this invaluable method of coping."
Spouse no longer drives at 78; I anticipated this change that occurred 3 months back to be a tremendous hurdle and it has not been for him. That comes under the category of "things dreaded that actually went well."
I most definitely agree with your opinion about covid placing folks in each other's pockets in households far too long.
I play the hand I'm dealt as follows:
We want to defend our honor by saying, "I did not do X," and that's the most difficult issue to scale back for me. A list of noncommittal answers helps: "How about that?" "Who would have guessed?" "Huh, no kidding." etc. and then I go Gray Rock. Please look up this invaluable method of coping.
It's going to take everything you've got to handle this, and many good wishes to you. One last thing is that I'm 67 and I was quicker on the trigger in my 50s. Coping has become easier but it's far from easy. If abuse escalates to physical, then all bets are off and get the law in on things. This answer is for your POV only and not medical reasons for his change in behavior; others know more about that than I do,
Im not suggesting your husband has Lyme (though you never know) but I am suggesting that there is every possibility that something is going on other than dementia, something that can be treated and needs to be treated before it creates havoc elsewhere. It’s very easy for all of us, doctors as well to get tunnel vision when it comes to medical symptoms because it’s natural to see what you know. Your DH like you may have a heightened awareness of dementia and live in fear of it based on his family history or his perceived family history and denial is a powerful coping tool so finding ways that feel less threatening to explore any possible medical issues might be the way to make that happen. I wouldn’t focus on his outbursts or his apparent attempts to “gaslight” you, I wouldn’t even mention his possible cognitive issues if you can help it but maybe getting his primary to recommend a neuropsych eval simply to get a baseline or so DH can “prove” his memory is fine if it comes to that. By life insurance to create the need for a full physical if need be or get someone, your child maybe, to ask if you have BOTH had physicals recently and urge you to do so, not because something is wrong but because they have a friend who’s parent just dropped dead of something that could have been prevented if caught early enough...be inventive about it and put your money where your mouth is so to speak by getting the full gammet yourself.
I also urge you to step back when he comes up with these things and try not to react to it as the personal attack it feels like, whatever is going on it’s more likely that he really believes what he is saying/thinking and is incapable at that moment of being convinced otherwise so don’t escalate both of you by trying. Granted I don’t always trust my memory but there are times my DH will suggest “someone”, meaning me, moved or lost something and I just agree (especially when it sounds stupid) and laugh “must have been me, I have no idea what I did with it” sometimes with a hint of sarcasm “your right it makes much more sense that I added a rotten potato to the bunch than one of them rotted on their own, sorry”. Wind out of his sails and a giggle for you.
Maybe it’s dementia and maybe it isn’t but all is not lost, there are proactive actions and reactions to help. withU
That was so helpful to me.
BUT, I JUST SAT DOWN AND TRIED TO FIGURE OUT--what should I do??? I cried, he cried, can't take it any more, on and on, every few days or weeks.
THEN it hit me--For Better or Worse. I suddenly realized, see a doctor. I made a list of things he does, I took this list to his regular 3 month checkup and doctor referred him to a neurologist . Tests, revealed nothing, slight vascular area, but good. Then as a year or so went on, still arguing but not as much, I changed his doctors and did the same thing, list of actions. Now, brain scans, and yes dementia causing these outbursts. From then he was a pussycat, and had low dose medication. Also, as others in this forum said, have him tested for UTI, as this can cause the behavior you describe. Hope this helps.
I believe I can share some good advice with you on this subject. A little on how I came upon these opinions. One of my favorite hobbies was public speaking. I watched my maternal uncle who was a Catholic Priest die of ALZ in his late 70's, I have always been a spitting image of him. My Stepfather slowly died of ALZ in his late 80's. I watched them bot deny-deny-deny, that they had memory issues. When I was 35 I began volunteering to do public speaking for a fraternal organization I am a member of.
When I first began my public speaking roles, I easliy soaked up the parts in to my memory. Public Speaking was a gift to me and over the years,, I learned more and more parts and I had a ball traveling around the state in which I live and Ii was mentored along the way by some of the best performers in our organization. Now, go forward 17 years and one of my parts changed and I could not learn the new script, this was in 2011
. I approached one of my doctors about the problem and he asked was I usiing my CPAP everynight. I never slept without it during the 16 yrs I was using it. I was also told it probably had something to do with all of the responsibility of managing the life of a Special Needs child which came in to the live of my DW and I when I was 48. I spoke to a couple of more doctors and they attributed my problem to all the same issues. Go forward 5 years after 38 yrs of my career, i was fired from my job in February of 2016. Finally, my Neuro doctor said, Wow, we've got to dig deep on this and she prescribed an MRI and a Neuro-Psych Eval. Four months after the MRI, we had the Neuro-Psych results which indicated a diagnosis of Early Onset ALZ one month before my 57th birthday, that was four years ago. Test results showed I was in the lowest 1% of all men my age in terms of the test results.
I can't tell you how relieved I was when I received the diagnosis. I started doing a lot of reseach and reading on Aging Care. A bit of advice I discovered was OK, I am never going to be cured from this disease and I retained an attorney to help me through the process of Social Security Disability. I was told by my doctor, I would not be being fair to an employer or my customers if I tried to continue working. The lawyer I retained worked for SSI as an Attorney for many years and retired in to his own law practice to help people be approved for SS Disability. I received my first check 52 days after the paperwork was filed.
I have made it my mission to share as much of my journey as possible here on Aging Care. I encourage any family members or readers of Aging Care to not be afraid and push your doctors to investigate any memory issues your think you might have.
Now, it has been 9 years since I first noticed I was having memory loss. My Neuro doctor tells me, I am the first patient that ever gave up their Drivers License Voluntarily without being told they should hang up the keys. I have had the same Neuro Dr. for 15 years and I brought up the subject of driving when I was first diagnosed. Every appointment we had over the last 4 years, she did a thorough exam and she said she was comfortable with me continuing to drive. Nothing untoward happened, no tickets, no accidents. I just felt uncomfortable driving and hung up the keys. Yes, it has added more to the load my DW has to carry, but she supports me and is accepting of the new role in our lives for both of us. We've been together for 26 years dating and married 24 of those years. We've never had an argument in all these years. I accept when I'm told I've forgotten something. I have been blessed with the most wonderful wife, and with our three children two of whom are adults, one a teenager.
I encourage spouses, children and those that think something may be wrong with your memory to stand up for yourself. We must be our own best advocates. I have made my instructions clear orally and legally to my family and doctors.
Good Luck.
Just in case, may I suggest that you make a video recording OF yourself, speaking TO yourself, so that later, should you slip into disagreement with your family, they can play it for you - - you might recognize and listen to yourself. Just an idea...
If necessary, go see or speak with the GP on your own and talk about what is happening. Those three examples are enough to see that something is not quite right. Avoiding 'whatever it might be' is not going to make it better. Let's hope there's a good explanation and some sort of treatment and get that doctor's appointment asap!
please get your husband in with good neurologist quickly to see what’s going on. Prayers for you both. I’ve done a lot of crying and praying, believe me!!
You need to change your attitude and quit taking it personally. That is very hard to do but necessary if you want peace of mind.
For example, in the rotten potato incident, you could say, I don't know how that got in there and simply remove the potato.
The accusation over the cell phone would be harder to turn away but maybe you could say, I don't remember that, and change the subject.
You have to know that this is dementia and not his normal behavior.
I think a thorough physical is the next step. You need to inform the medical team what you are concerned about so they can perform testing.
They may need to add certain markers in their blood work that they normally wouldn't test for or add other tests that cover this area.
Clinical studies connect microdoses of lithium with amyloid plaque ( which causes Alzheimers) reduction and cognitive improvement. Lithium is an essential element from the earth we normally would get in healthy food, but our soil and food are depleted. Here are the studies. It's worthy doing the research .
https://content.iospress.com/articles/journal-of-alzheimers-disease/jad190862?fbclid=IwAR00XaWA0BUr0BQqnnYC1D4nVSx4jpkes9uhhWiBFKIQQ3YvdgY8-3ZNEzY
https://scitechdaily.com/low-dose-lithium-may-stop-alzheimers-disease-in-its-tracks/?fbclid=IwAR0FwmWc3hXCadTbRzsnGIndR3LhXD26ohsL_gwQ9Fkqq6m21fHlHB1CZ4k
https://www.psychiatrictimes.com/view/lithium-alzheimer-prevention-what-are-we-waiting?fbclid=IwAR2hnjyERcF-sre0Ooqczoxk1nrSoeqgWUyAHIJ9dCSGvi4E9hSz1rnWf6A
Which is why medical evaluation should be sought whenever there is a noticeable deviation in behavior. Best to find out what you're dealing with diagnostically, the sooner, the better.
Here is an article about different causes from the UK: https://www.nhs.uk/conditions/dementia/causes/
Here is one from USA: https://www.webmd.com/alzheimers/types-dementia#1 I just did a search for Causes of Dementia and found these two articles. There are many more, but I read these and thought they might help. This is a really thorough one: https://www.mayoclinic.org/diseases-conditions/dementia/symptoms-causes/syc-20352013. Praying that you are able to find answers soon.
unfortunately, as I read your question and descriptions of behaviors, I do think your husband is starting dementia. I lost my mother last December. LBD. Upon reading your husbands behavior reminded me of exactly similar behaviors my mother had at the very beginning. Very early. Now I understand why she was accusing me of silly simple things that I didn’t do. She was confabulating. Later, other symptoms developed which were extreme and hard to handle. But your descriptions match my mother’s very very early stage.
It’s a journey of 7 to 8 years. I’m sorry to tell you, it will get worse.
all I can tell you is to cling to God very tight. Do not argue, do not try to convince, do not engage. When possible re-direct.
may God bless you and accompany you.
It appears that something is going on with your husband's thought processes. It could be blood chemistry imbalances, one of the above dementias, or even a tumor. Please get him to agree to a doctor's appointment so you can pinpoint the problem. If he does have early Alzheimer's disease, there are wonderful medications that will help him have better thought processes for many years. The key is early diagnosis and treatment.