Tick Tock

 

“I stashed all the clocks in the attic today,” said mom’s caregiver, who fills in when I’m gone. “Time is really stressing her out.”

Clocks and calendars are a cacophony of confusion for mom. Adrift on the time-space continuum, she’s never certain of the day of the week, the season, whether morning or night. “I’m having trouble understanding August,” she confessed and pointed to the calendar, now as perplexing as her windup clock.

Not being able to keep track of time makes her anxiously ask what time it is. Yet as soon as I answer, she’s forgotten the whole conversation and asks again.

At first, I didn’t get it. But I learned that as a result of lost brain functions, people with dementia can’t judge the passage of time. Since mom can’t remember what she’s done in the immediate past, she has no way to gauge how much time has passed.

When I finally accepted this, I received an unexpected gift: compassion.

The clocks may be hidden, but their numbers remain forever jumbled in her mind.

This Old House

This year marks the thirtieth anniversary of my move from New England to the West. My parents, long-divorced, still live on the East Coast. As they come to need more help, for the past three years I’ve shuttled between family life in the desert and back east where I grew up.

My caregiving horizon goes beyond taking care of people. Its broad tentacles encompass houses and pets, too.

As household manager of multiple households, my resume skills have expanded: family caregiver, Power of Attorney, financial expert, property maintenance. I handle new generators, furnaces, and plumbing systems, not to mention leaky roofs and a mouse infestation for two century-plus houses. Mercifully, my husband oversees the house in the West.

Like my first exposure to dementia, I knew nothing about old houses. And, like dementia, nothing is certain with an old house.

Betwixt & Between

I began this journey with an absolute: mom will never move to a care home. As months turn to years and mild dementia transforms into moderate stages, I learn there are no absolutes with Alzheimer’s.

Mom is a “tween” – in stage, not age.

She’s in limbo, and I live it with her every day. I stay with her in the home of my childhood, for long periods at a time: cooking, entertaining, watching and waiting. This summer I visited dementia care homes. Mom’s name is on five waiting lists now. Guilt mingles with relief.

When I go home to recharge my batteries, our paid caregiver takes over, a transition as anxiety-ridden for mom as a simple change from orange to apple juice. The caregiver comes every day; this time I’ve added one overnight a week.

Rule #1: Never say never.