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Neurologists usually have waits for appointments, so I suggest getting an appointment scheduled. You don't know how her condition is going to progress, and you may need a specialist for symptoms that arise. It will be much better to already have her established as a patient because they will address your concerns more quickly than if you have to start from scratch on a waiting list. Different forms of dementia manifest symptoms in different ways and may require a specialist to prescribe treatment. Better safe than sorry, I think.

Does anyone have your mother's POA? If so read what is required for it to be activated. It may require a written formal diagnosis.
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Reply to MG8522
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I took mom to a neurologist which was a total waste of time. Her PCP's PA was far more versed in the everyday life and difficulties of dementia than a doctor who sat behind a desk was. When I asked the Neuro if it could be Parkinson's mom had, she asked mom to touch each of her fingers to her thumb as fast as possible. Then said Nope, it's not Parkinson's. 🙄
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Reply to lealonnie1
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My father had dementia. We never took him to a neurologist. Had he been violent or combative, we might have done so. We relied solely on his PCP.
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Reply to Hothouseflower
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Neurologist just had Mom draw the clock face at a certain time on every visit. We did not get much out of it.

Mom would practice drawing clocks 3-4 days out.
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Reply to brandee
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Depends on what you would need the formal diagnosis for. The insurance company sent their own nurse out and she gave my LO a brief verbal test and that was all that was needed for a formal diagnosis to have care covered for the insurance purposes. My LO didn't even know that's why the questions were being asked.
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Reply to ItsaBattle
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I would not trust my LO to a PCP when it came to Dementia/ Alz. I took my Mom to a Neurologist for testing and medication.
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Reply to JoAnn29
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Make sure she has legal paperwork in place granting someone POA first, because once a person is diagnosed with dementia they are considered legally incapable of managing their own legal or business affairs.

I am a bit surprised that whomever prescribed the MRI didn’t offer a diagnosis.

If your mom is already in a safe situation and manageable — in assisted living, not handling her own finances, not driving, with people nearby to help with meals, laundry, fixing things, etc — and she’s not causing problems for herself or others — diagnosis is less important.

OTOH if she is living alone, acting dangerously or inappropriately — giving money away, driving and getting lost or having accidents, at risk of leaving burners on or doors open all night or wandering, etc etc., and resisting your taking steps to stop all this — diagnosis would be quite valuable as it gives the person with POA the power to take charge.

You don’t mention any of this, but If she is prone to rage or combative or obsessive behaviors or staying up all night getting into mischief, meds can help and for those you need a diagnosis.
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Reply to Suzy23
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I believe knowledge is power. You may learn valuable information from the neurologist visit and testing. This can be a long journey and knowing more can prove helpful
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Reply to Daughterof1930
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How old is your Mom?

If it were me I'd get a formal diagnosis, but it doesn't have to come from a neurologist (there aren't enough of them so are very busy and hard to get in for appointments). A good Primary can make the diagnosis after discounting any other causes.

Even if she doesn't have a PoA that requires a diagnosis, it will be helpful if she ever needs meds to address her symptoms.

I hope she has a PoA assigned and if not, I would encourage her to get this in place without delay.
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Reply to Geaton777
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It might depend on whether you will need a formal diagnosis for anything. For example some POA documents require an official statement/diagnosis of incapacity. Or some memory care residences may require it. It might be helpful in accessing some benefits, I'm not sure. It's not going to help with treatment, unfortunately, since there really isn't much out there.
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Reply to Slartibartfast
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JoAnn29 Jun 30, 2026
In my State FPOA is automatically immediate unless stipulated differently by the person assigning it. Medical needs a doctor saying the person is not longer competent to make informed decisions.
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You might want to see if your community has something like a “center for aging“ where there is a doctor who specializes in the aging population. A neurologist might not be necessary. when my mother was originally diagnosed, that’s how we did it—through simple cognitive testing in the doctor’s office. Once she had been diagnosed with at least mild cognitive impairment, she went on donepizil and the doctor said as long as she didn’t progress, that would indicate that it was not Alzheimer’s. This type of medical practice has a lot of information for you as well as for your mother. I think you might find it very helpful to find someone who specializes in aging like this.
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Reply to BabyGirl2
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