← Return to Anesthesia related cognitive decline, specifically dysnomia

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@naturegirl5

@pb50 Pam, this is great! I’m so relieved that the neurologist spent enough time with you to get a real sense of your concerns. Did the neurologist give you a Mini-Mental Exam or the Montréal Cognitive Assessment (MoCA)? These are both quick cognitive screeners but they are just that. A screening test to help figure out if more testing is warranted. Anyway, the MRI and neuropsych testing will be far more helpful in figuring out your cognitive changes that you describe so well here.

I’m so glad you have a plan. I’m going to look up the vitamins and minerals that you are tested for. Thank you for posting that.

What’s next? Working on the changes in your diet? I’ve done the same on the advice of nutritionists I have seen. It’s a challenge and one nutritionist advised me that if I’m about 80% compliant with the healthy diet I’m doing really well. That was encouraging as I tend to beat myself up if I “go off the rails” and eat something from the unhealthy list of foods.

What kind of exercise do you like to do?

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Replies to "@pb50 Pam, this is great! I’m so relieved that the neurologist spent enough time with you..."

No .. I had the standard dementia screening - remember these items, draw a clock, draw the hands showing this time, some simple math word problems, etc. I’m pretty sure I passed that 🙂

The doc has a PA who administered the mini cognitive tests and high level history/chief concerns, and a med student who execute the time consuming pieces of medical history and drafted the visit notes and summary.

He is starting a monthly seminar-workshop for avoiding dementia and the first one is tomorrow afternoon and I’m going.

I don’t cook. I’m the queen of frozen entrees and take out. I can pretend I’m going to change but I won’t. So I need to find a Mediterranean restaurant I can
order takeout from.

Being proactive seems productive.