He knows me, he knows me not

«That’s not a very LBD thing,« my support group leader mentions. It’s not, and I resent that. There had been «a promise« that I would not be forgotten. The word was people with Lewy Body Dementia tend to always remember their loved ones. It’s not like Alzheimer’s. Well, Burt knows I am important in hisContinue reading “He knows me, he knows me not”

Here’s where the focus shifts

Burt is having more interactions with hallucinatory visitors these days. He experiences delusions and a good deal of confusion. This lessens his involvement and connection with those of us with him; the ones actually in the room. For instance, when I told him I was his wife and I was home with him, he said,Continue reading “Here’s where the focus shifts”

His decline. My denial

Oh, that famous river is always right over my shoulder. Is it my heart that keeps me from accepting the inevitability of this disease? Burt has been declining, as in sooo much more confused, delusions and hallucinating to beat_the_band. He also is often sleeping more, although the fact that he’s up half the night contributes.Continue reading “His decline. My denial”

Rapid

My sense is that Burt started his path in LBD at an advanced stage. From the get-go he went from a period of apathy to being fully confused in what felt like 60 seconds. Capgras was one major symptom; little people enhabited our home; he needed reassurance that he was home. Meds helped a lotContinue reading “Rapid”

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