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Marcilina Martel's avatar

Vicki,

This part you wrote:

The cramped seat terrified him. The crowds were too much stimulation. His world is getting smaller and no amount of love or planning or hoping can make it larger again. That is the disease. That is not you.

I appreciated how you captured how he felt, terrified and afraid. As caretakers we often talk about what we go through, what we watch leave us, what we deal with everyday- watching someone loose pieces of themselves. But it’s so hard to watch someone feel afraid and they know things are changing for them and sometimes they can’t even put words to it, they just know they’ve changed. It’s frustrating to them. It’s painful for them.

Thank you for sharing your story. 💛

Pam Johnston's avatar

My husband has Parkinson's dementia (a form of Lewy Body Dementia), which is different from Alzheimer's in many ways--but everything you've described here feels precisely accurate. (I often wondered how it was even possible for him to perform this kind of normalcy when, on a typical day at home, he struggled to put together a coherent sentence.) Now he's in memory care and a hospice nurse comes to check on him each week, so he doesn't have to perform for anyone. We're all on the same sad page. This is both easier and more difficult for all involved.

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