Memories

What makes you feel nostalgic? A YouTube video of snow cascading outside a coffee shop with jazz pleasantly playing prompted «It’s a slow game, but it’s good« from Burt. Lately, Burt will comment on a “movie” he feels he’s watching even with the TV off, so mention of the «game« didn’t throw me. For me,Continue reading “Memories”

A timeline

Burt had a sudden downturn starting in October. Although I have documented Burt’s decline, I am still unsure of the actual events. His decline has been incremental and gradual. It has also come on suddenly, precipitously and unexpectedly. In October, things like confusion and hallucinations seemed more noticeable. Soon thereafter, one of his aides andContinue reading “A timeline”

It’s never too late

The jingle about Jello Instant Pudding® is running through my head right now, but honestly this is a serious post about a serious question. The other night, Burt, in the midst of his confusion, was lamenting how “sick” he feels. My response was to tell him that whatever was bothering him, hurting him and upsettingContinue reading “It’s never too late”

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”

Foodie

Sometimes, something just predisposes us to enjoy a food. Cooking has been pretty much out of my vocabulary for quite a while. My favorite “meals” lately have involved some measure of yogurt, usually with nuts, fruit, and granola. (No hot food, so maybe that was what  predisposed me.) I mix a breakfast cereal mush forContinue reading “Foodie”

Burt says

Marriage is hard. First, you have to love the person and then it’s a lot of work. Burt advises some “friends.” His conclusion is that all “those 30 people over there” will think twice about getting married. He was having a lucid, although clearly not hallucination-free, morning. I value the days when he knows whoContinue reading “Burt says”

There’s a lot to be said

From pretty much day one of Burt’s symptoms, I looked to getting help. Initially, it was because I needed my time. I wanted to get 3 or 4 hours several times a week to get out. It seemed an existential need for me. In the parlance of our dementia communities, it’s deemed “self-care.” Some ofContinue reading “There’s a lot to be said”

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