Does the MMSE take low IQ into account when testing for dementia? My DH is a genius at mechanical things. He can fix just about everything and even investigate and find a hard to detect issue (like a short in our RV that took him 2 days to track down to a very unlikely source but he did it!). However, at everything else...he is fairly clueless. He struggled through school and barely graduated from high school. He has a hard time following plot lines on TV shows and movies, he does not read unless it is about RV's or cars or camping, he gets confused about his doctor appointments and medications, has a hard time following conversations, cannot cook or do laundry or plan a dinner or host friends or family. I do all of that plus our finances. How can he be brilliant at mechanical things but barely get by on almost everything else? His MMSE score was 25. The neuro says he is "borderline" and wants to see him in 6 months and perhaps every 6 to 12 months thereafter. I am concerned that he may score lower at his next exam and test but that it is his IQ and not necessarily a cognitive issue that causes the low score.
As a dementia screen, they should be using a test equivalent to the MoCA or even better, the ACE-III. These both take into account a person's educational background, and they include questions regarding executive function - this is one of the most important areas to assess for dementia, as well as memory function. These tests can be repeated at intervals to see if there are changes over time - but repeat tests are only useful if the doctor/nurse puts the date of the test on them! Make sure they do.
Of course, the MoCA and ACE-III are only screening tests. If they note areas of cognitive decline, you should request a more comprehensive assessment with a qualified clinical neuro-psychologist.
Just as an aside. My husband later admitted to me he has felt” broken” his entire life. It’s horrendous the way this condition is viewed.
Undiagnosed/undertreated ADHD can lead to all kinds of mental health issues like depression and anxiety. I hope your husband can get whatever help he needs.
Intelligence is hard to measure because people learn differently and people never learn what doesn't interest them.
Some people have many gifts and talents, while others may have one great gift or talent and that is your hubby! I am sure your hubby does have other gifts and talents...its just that one (mechanical) over shines everything else!
I agree with Moecam.
As far with the next test can you tell the Neuro about your concerns without hubby or write a note or email, or perhaps a phone call.
I hope he gets the help he needs:)
Good luck!
The fact he graduated high school & if he has a learning disability then in fact he is quite smart but tests won't show this - the fact he can't cook is an example of how he can't grasp some ideas - he probably told you he wasn't very smart over & over again because that is what he was told as a student ... & you have bought into it from habit - schools generally had a track to get as many drs & lawyers & dentists as they could that they tend to ignore/under-rate other streams as 'not quite up to snuff' therefore not worthy of giving much attention
So please don't continue thinking he has a low IQ but rather take a little time to read up on learning disabilities with an open mind or even talk to someone who would know about it to narrow down the focus - he can't have as low as IQ as you say because he obviously held a pretty good job for a long time in order to be able to afford to get an RV! - you may have a new light on him after this
Also he is smart enough to have conned you into doing everything didn't want to do
One thing that I hadn’t considered till going thru tests with my mom was language background. Huge issue for those whose first language was not English. For a lot of those tested now in their 80’s or 90’s they easily could have come from homes where as a baby or toddler it was not an all US English household. Like they had a German grannie that lived with them or grew up in a more Nordic community or immigrated pre WW2 as a child or were WW2 war brides. Even tho now they speak perfect non accent US English, as they age and cognition declines their early knowledge stays imprinted longer and what they learned later fades out first. They know the answer but cannot answer in English as they have issues processing due to dementia PLUS translating. It’s a rare gerontology program that can do testing bilingual.
for anyone reading this, if this at all describes your elder, their testing may not be accurate.
Cannot wait till the only used to digital time devices group starts getting asked to do clock drawings.....
I'm not sure how it would affect a dementia test but I know an adult ADHD specialist was able to rule out dementia when he diagnosed my husband with ADHD
When my mother was diagnosed with vascular dementia they asked things like her birth date, who was president, memory rather than general knowledge but relied on CT scans that showed areas of brain death/ damage
You can choose whether this evaluation is helpful to your spouse.
What is the purpose? To get meds? To get admission into a nursing home?.
The Mini Mental is an old test and is only effective if the patient is willing and eager to please. A distressed, hard-of-hearing, apathetic, visually impaired, depressed or disinterested patient may not really “try” anyway —then they leave the appointment branded forevermore wiith dementia. They can go back every six months, like clockwork a pawn of automatic self-referral, to be administered the same or similar test, to be made to feel less than adequate. Squeeze those appointments in with the hundreds of others and your retirement is spent in the misery of doctors’ repeated evaluations, scrutiny and criticism.
So Emma Thomason lives at 3497 Johnson Road in Somerville. She is an avid quilter and golfer who plays the lyre and reads about philosophy. Remember those facts. Focus on those facts. Wait through two minutes of awkward silence. What’s Emma’s address? Huh? What does this prove? Zero.
i took Dad to doctor after doctor and therapist after therapist following his stroke. He was getting speech, physical and occupational therapy. He was having necessary dental work. Dad was on Coumadin for which he needed monitoring and saw a cadre if other specialists for monitoring for other reasons. Dad thrived with positive feedback. He regained reading (after losing the ability following a stroke). Trips to the neurologist were depressing, caused emotional and mental setbacks and proved no other useful purpose. We tried two different neurologists, but it seemed like a useless and humiliating exercise.
Dad only received care at home and was never prescribed the drugs that purportedly are supposed to enhance or preserve memory.
There was no need for him to endure this semi-annual humiliation. Otherwise, he was doing quite well. So with the blessing of our primary care (and other specialists) we opted out of the neurologist.
My cousin suffered from dyslexia. If it wasn't for his Mom pushing for him he never would have gone to college. Its not that he can't read, its how he sees the words. He was taught ways to overcome this. His strength, the gift of gab. His job, a salesman making 6 figures a year. My cousin will be 57.
Your husband fell thru the cracks. Sad to say, even now parents have to fight the school system to get what children, by law, have a right to have. Because, when there is a special needs student, the school has to pay out of their budget for what that child needs. The schools will fight not to have to do it. So parents have to know their rights.
There is no such thing as "no child left behind". Teachers have 25 to 30 students and you really think they r going to take time out for one student. No.
It would be so nice to find out what ur husbands learning disabilities are besides the dyslexia. But then that could be the main thing. He may feel so much better about himself if he finds he is not "dumb" and there are good reasons for his learning problem.
Please come back and tell us what u find.
I just read your comment wondering if your husband might have been "faking" all the abilities he displayed for the first five years of your marriage.
No. How? I've heard of selective INcompetence before now, but not selective competence.
Unfortunately, it is the loss of those routines that is something to worry about. But don't panic - you're a long way off having any bridges to cross.
It sounds as though the hurtful turning a wrench remark was a memory that was triggered by a comment that your husband found critical, even if you never meant it to be. The key thing is that it wasn't true then, and probably isn't now.
It also struck me that my mother claimed to have done badly on cognitive tests because she couldn't sustain an interest in "these trivial questions." She also said she couldn't be bothered to name the Prime Minister because he was such a nonentity.
So all in all, I would agree that your husband is sending out a fair few signals. Hearing loss is a further problem, and a bit of a chicken and egg one. Loss of stimulation is not good for the brain; loss of neural pathways is not good for processing sound. Does he by any chance enjoy singing? - singing in the shower, singing in the choir, any singing, doesn't matter what.
To my mind, he just shows how pitifully inadequate our methods of assessing intellectual ability are. The range of skills and the brain processes involved are complex and poorly understood, and most means of assessment are therefore rather clumsy.
"Word blindness" is a phrase you may hear when he trips over on that "spell world backwards" poser - but visualising the letters is only half the game, at best. There are also all kind of auditory elements that go into a process that most people manage so naturally they're never aware of what their brains are doing.
Your husband probably missed out on the attention that is nowadays paid to the various dyslexias but I'd guess there is some form of that at play. We went through this mill with my son: long story short, when tested again at age 16 he had developed a wide range of "coping" strategies to compensate for whatever brain links were missing. Except one. He cannot, not to save his life, understand or do "Spoonerisms" - the word play where you swap initial letters, often to humorous effect, named after the Oxford professor who famously berated a student with "you have hissed all my mystery lectures, you have tasted two worms, and you must leave Oxford today by the town drain." I was told by the educational psychologist that this is the test they save up for last, because it is a dead giveaway. 3/30, he scored, and I suspect he guessed those three.
I also know a very successful Art Director who can't reliably spell his own name.
It is a crying shame that your husband's needs were not identified and addressed; but then again he hasn't done so badly, has he? :) He did find things he was good at, and he has enjoyed a worthwhile and productive life, and whatever his difficulties a low IQ seems not to be it.
As for how or whether this will affect his cognitive assessment and possible dementia diagnosis... If you're really uneasy, talk to the psychologist, neurologist or psychiatrist who's running the test and ask for a close look at where the gaps in function are. If he's *only* falling down on questions where his known difficulties are relevant, that wants taking into account. But in dementia, the big clue is when things a person did as second nature - using a familiar route, wiring a plug - are suddenly just not working right. You'll know it when you see it.
I would discuss this with the doctor conducting the tests prior to the testing.
This might be something to bring up when making the appointment, ask if the doctor does this and if they say no then I would look for another doctor that would.
Funny thing when my Husband was given a MME the three words he was asked to recall were something like ..denim, satin, corduroy.. I said if he had been asked to recall hammer, screwdriver, wrench he probably would have recalled at least 1 of them.
I think a good thing to remember is no one should rely on one test to diagnose any condition.
His drawing of the clock with numbers & hands was so telling... and when people will voice concerns about a loved one, I advise the clock drawing. Of course, your right about just one test... on the day long testing, they give a myriad of tests.
DH does sounds very much like he may be on the autism spectrum. I have two kids on the spectrum, and they are both extremely different in how it affects them. I haven't really come across any studies on how dementia may affect an individual on the spectrum...but something to perhaps look into. Society still kind of doesn't think about kids with autism growing up into adults and even potentially elderly while still with the autism. But getting diagnosed later in life is on the rise now that more people are becoming aware and getting their "quirks" checked out. I'm actually curious myself now about dementia and autism that I've seen your post. I definitely would suggest asking his neuro to test for autism (not IQ, it's kind of moot at this point) and then go from there.
If that is only test you are relying on, consider other contributing issues and evaluations for. But that score alone is something many of us would have welcomed.
People with autism DO NOT generally have one thing that they are good at - because they were born with a “gift” in that area. It is because when an individual with autism becomes interested in something - they are all in. Focusing to the obsessive extreme is common. That’s why they are good at a particular subject.
It is true that there is a higher rate of savant-ism among individuals with autism than is typically found among other groups. But being a savant is waaaayyy different than merely being good - or even very good at something. Ergo- just because someone has a talent AND they are socially awkward- do not jump to an autism conclusion. Think the movie Rainman. He was a mathematical genius- a savant. And, that is the exception not the norm. Only 10% of individuals with autism are savants.
For other symptoms of autism - beyond the stereotypes- please go to an informed autism web site. Autism Speaks and Autism Now are both good.
There are many different IQ tests, and lots of argument about them – do they favour vocabulary (most do, but is that fair?), or patterns, or mental arithmetic (same questions). Are they ‘culture fair’, even fair in requiring reading and writing skills (obviously not)! Rather than ‘low IQ’, it’s probably a better take to say that his intelligence is atypical, and that might make both of you feel better too. I hope you love each other, and manage to make as good a fit as DH and me. Best wishes.
Also, while his heaing tests are fine, his auditory processing tests were below average. This will skew any test given verbally.
Dx Autism (high functioning) but called Aspergers by others. Now called ASD Level 1 in DSM 5. Before that dx, some teachers & other parents had already labeled him: disruptive, uncooperative, hearing impaired, learning problems, a problem child.
He also used to spin in circles at 5pm & wander aimlessly about the house like a sundowners pt. It was caused by mental fatigue.
I agree with JoAnn29 - definately ask your Doctor what he knows about Autism. You want him dx correctly.
You may want to contact an Autistic agency in ur area. Ask them what they think. Maybe they can do some testing. Just read that Autism is a neurological disorder. May want to call his doctor and tell him husbands history. It may make a difference in his diagnosis.