← Return to Husband With Slow Cognitive Decline: So sad & confused

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I think the neuropsych testing is important to create a baseline for the person’s mental status, for comparison with future testing. My husband’s testing was 8 years apart and looking at the DATA really helped me realize and accept what was happening and what it meant. He was very good at disguising his deficits and I was the frog in the boiling water, making ongoing adjustments but not realizing how bad it was getting. Your PCP can refer you to someone in your area, It takes about 3-4 hours over 2-3 visits, with plenty of breaks. My husband really enjoyed the testing- lots of puzzle-type things, word play. The tests are set up for thinking skills, there is no “wrong” answer, so the person doesn’t feel they’ve done poorly or get upset at a difficulty.
My husband has a breakfast/lunch place he loves, so I always talked up going there after a session- keeping things positive. He likes and trusts his PCP, so I just told him Dr wanted him tested for memory, no big deal.
Later, I met with the neuropsychologist, by myself, to go over the results and the comparison with the older testing. I though that was best- no need to upset my husband, he knows his diagnosis, but thinks it’s just some memory problems. I could ask straight-forward questions, as many as I wanted, to more fully understand what was happening and what the future would probably look like. I shared the results with close family. The DATA was really helpful for their understanding too. You see stuff, but you don’t really get it/understand it.

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Replies to "I think the neuropsych testing is important to create a baseline for the person’s mental status,..."

Thank you so much for this reply! I was not clear in my first post…we have had the cognitive testing, several hours over a couple appointments. Once with a NP, and two appointments with different neurologists, plus a neuro-psychologist. So the testing results are recorded…and we will go again at some point. We also joined a zoom group with the Alzheimer’s Association, but some of the folks were so far beyond my husband’s diagnosis of MCI that it upset him to see them. We ended up not staying with the program, though I found it helpful and supportive. Your idea of speaking with his PCP to suggest repeat testing does make sense. I hate tiptoeing around behind his back, as we have never done that, but perhaps the benefit is worth doing that. Again, thank you so much!