Mild cognitive impairment: What questions to ask the neurologist?

Posted by sb4ca @sb4ca, Jul 8, 2023

I have been having increased problems with word retrieval, forgetting the subject in the middle of a discussion, not knowing how to spell words that I've always spelled in the past, missing important meetings etc. My neurologist had me take a cognition test and did an MRI. Both showed mild cognitive impairment. I really don't know how this advances or how rapidly. My meeting is tomorrow. Does anyone have suggestions on what I should ask?

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Oh I’m aware. But the drugs get to the infusion room via a central pharmacy in the hospital. In a Doctor’s office in my experience there is a mini pharmacy - same kind of controls. Particularly as it relates to opposing drugs.

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@SusanEllen66

@pb50
First, I’ve already had an idiopathic brain bleed several years ago.

Currently, I take full strength aspirin every day because I have a history of A-fib.

Thirdly, I have a rare autoimmune disease that has caused my arteries to become inflamed.

The black box warning on Lequembi is very clear. People who have these problems should not be given the drug.

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My mistake. I didn’t grasp that from initial read.

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@pb50

You’re on a blood thinner?? I would think pharmacy would catch that. But agree more discussion needs to take place on that.

That said, I am on an infusion drug for Rheumatoid Arthritis. The warnings are scary - including notable cancer risk. But I have to try to manage the disease. So I accept that risk.

I have recently been diagnosed with mild neurocognitive disorder. My research of available drugs and many promising trials describes that to get drugs past the blood brain barrier where they might do some good introduces bleeding risk. But a drug can’t reduce amyloid plaque - the holy grail of Alzheimer’s treatment - until it gets where it is - on the other side of the barrier that prevents certain substances from getting to the brain itself - the blood brain barrier.

For me your decision is about what scares you the most. For me it is the disease itself. I watched too many family members spend 10 or more years on a path to cruel and horrible death.
I’d prefer to accept a risk that I go out fast. But that’s just me. And while I accept there is bleeding risk, it’s just that - a risk.
If it were more likely than not, it wouldn’t have made it this far.

So I’m surprised and sorry these risks weren’t spelled out for you. Too often Docs don’t think we can handle or even understand the truth. But that explanation is why they get the big bucks. My suggestion is that you force that discussion.

Best of luck.

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@pb50 do you take Methotrexate or Rituximab for your RA?
I’ve done both for a rare autoimmune condition I have. The rheumatologist had to take me off Methotrexate because it was damaging my lungs. My blood oxygen levels got low, and test results showed ground glass opacity in my lungs.
Now I take Hydroxychloroquine.

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I took methotrexate when I was on Humira but it had to be lowered to the point where I developed antibodies to Humira. Switched to Enbrel and injected the methotrexate but continued to have liver impact. So I had to stop it altogether and switch to infusions of Remicade four years ago.

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I have minimal cognizant impairment. They started me out with a cognizant test which appeared slightly lower than average, but I am 67 years of age. The neurologist suggested I needed a psychiatrist for further studies - I did see him, but thought it was uneventful. I did fore go through an MRI of the brain and it did show a mass. So I decided to look into that and had laser surgery to have it removed. It was normal studies until about one year, and it returned. So I decided to go to a specialized oncologist -he went over several possibilities for treatment. I decided with his suggestion to go through a high dosage of chemotherapy . I have had a normal MRI for four years. Just goes to show you more studies are important. Good luck.

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