

Frontotemporal dementia tests are usually requested too late, or not at all.
“Dad Just Doesn’t Care Anymore.”
That’s what my cousin said after her father cracked a wildly inappropriate joke during dinner.
She didn’t know what to say. It wasn’t just a one-time thing.
He was forgetting to pay bills, leaving the stove on, and laughing at the wrong moments.
And not in a “he’s getting old” kind of way. Something was off.
That’s where it all started. Her family weren’t looking for a “diagnosis.” They were looking for a reason why someone they loved was becoming unrecognizable.
Turns out, that reason had a name: frontotemporal dementia.
Let’s make this clear:
When someone starts acting rude, impulsive, distracted, or disinterested in people… it might not be “just old age.”
This is what FTD looks like in real life:
These are not “moods.” These are signs of brain degeneration in the frontal and temporal lobes.
Doctors miss it. Families ignore it. The person going through it often doesn’t even know something’s wrong.
Here’s why:
According to the Mayo Clinic:
“Some people with frontotemporal dementia have changes in their personalities… They become socially inappropriate and may be impulsive or emotionally indifferent.”
Translation? They say what they want. They do what they want. They don’t feel what they used to feel. And it’s not their fault.
Here’s the thing…
FTD isn’t diagnosed in one shot. It’s a process.
And the most important part? You have to ask for the right tests. Most primary care physicians will not catch this unless you push.
These measure:
What you’ll hear:
If the answers are scrambled or delayed, it’s a red flag. But that’s not enough.
This one takes hours. And it’s worth every second.
It gives a detailed cognitive profile. Not just “pass or fail.” It shows exactly which parts of the brain aren’t working the way they should.
Quote from MSD Manuals:
“Neuropsychological testing can help identify the specific pattern of cognitive decline typical of frontotemporal dementia.”
Ask for it by name. Don’t wait for them to suggest it.
Why? To rule out other causes of behavior changes like:
Not glamorous. But necessary.
This is the turning point. With FTD, MRIs often show frontal and/or temporal lobe atrophy—literally brain tissue shrinking.
If the scan looks off, they’ll move forward with the next one…
This one doesn’t show structure. It shows brain activity.
Low activity in certain brain areas confirms that the symptoms aren’t behavioral—they’re neurological.
A PET scan is like watching the brain on “night vision.” If the lights are dim in the frontal lobe, something’s seriously wrong.
When they got the official call, the neurologist said:
“It’s behavioral variant frontotemporal dementia.”
That was the moment things got real. It wasn’t a phase. It wasn’t stress. It wasn’t her Dad being Dad.
It was his brain breaking down quietly and systematically.
Here’s what changed after her family knew:
If your loved one is…
…you need to stop guessing and start testing.
FTD will sneak up on you. It doesn’t look like memory loss at first. It looks like someone being rude, mean, or lazy. And that’s why families miss it.
But once you have frontotemporal dementia tests diagnosis, you can stop fighting the person and start fighting the disease.
Don’t wait until it’s too late.
If your gut says something’s off, you’re probably right.
Get the tests. Get the facts. Get ahead of the disease.