Perspectives

The Comfort of Ordinary Days

Photo of Breck SchubbDr. Breck Schubb, PT, DPT
4 min read
person with suitcase on left, chair on porch on right

August has a way of feeling like it's already ending, even in the first week.

The pool's still open, the grandkids are still around or on their way, but somewhere in the back of a caregiver's mind, the countdown has already started.

I've been living that countdown in a very real way this summer. Between one daughter deep in swim and water polo with travel tournaments, and another competing in travel dance, my schedule has been almost unrecognizable. Hotel room beds, dinners at whatever time we could manage, workouts that just didn't happen, meals that were whatever was fastest. My own routine completely fell apart. And if I'm being honest, I'm so ready for September.

That's the thing about summer. It runs on breaking routine on purpose. Later nights, someone else's guest room, dinner whenever everyone finally sits down. For most of us, that's the whole appeal.

It works differently in a house shaped by dementia.

The same visit, with a different bedtime and dinner at seven instead of five-thirty, can leave a person living with dementia more confused by Thursday than they were on Monday, more agitated in the evenings, harder to settle at night.

Here's what made this summer both humbling and clarifying for me. While my own head was spinning trying to hold everyone's schedules together, the woman I care for was steady. Different people were coming through the home. My presence was less consistent than usual. The household energy was different. And yet she did well. Because even when my routine fell apart, hers didn't. We held her schedule, her meals, her walks, her familiar daily rhythms, even when everything else was moving around her.

She didn't notice my chaos. She noticed her routine. And that was everything.

Families sometimes notice a harder week and blame the visitors, wondering if they shouldn't have had everyone over.

It was never the visit.

Routine is doing real work for a person living with dementia. The Alzheimer's Association names structured routine, along with a steady environment, as a first-line way to ease anxiety and agitation, ahead of anything clinical. When a brain can't reliably predict what's coming next, a stable schedule becomes the thing that still can: the same chair, the same walk, the same show at four o'clock. None of it is exciting. All of it is orienting.

That's worth remembering as summer winds down. Going back to normal isn't a letdown. For a lot of families, including this one, it's the good part.

Every September, quietly, the schedule settles and the visitors go home, and the Tuesday that follows can feel almost exactly like the Tuesday before it did back in June. For someone living with dementia, that sameness is often the closest thing to feeling like themselves.

It's worth honoring the caregiver who protects that unglamorous routine all year, the same breakfast, the same radio station, the same fifteen minutes on the porch, even though nobody applauds it. And it's worth honoring the person living with dementia who holds onto that same walk or chair, not out of stubbornness, but because it's one of the few places left where the day still makes sense.

This summer taught me something I already knew but needed to feel: you can be a caregiver in full chaos mode and still give the person you're caring for a sense of stability. But it requires real infrastructure. It's not just willpower.

We built Vallige around that idea: the ordinary, repeated moments matter more than the exceptional ones. Daily Digest happens at the same time every day, with the same familiar presence, whether or not the rest of the household's schedule holds together. Coordinating with the wider Village can mean routine bends less when life gets full, and finds its footing faster once things quiet down. For me this summer, that wasn't theoretical. It's what actually worked.

Somewhere ahead is a Tuesday in September that looks nothing like a Tuesday in August: quieter, fewer obligations, asking less of everyone. And on it, someone living with dementia will sit down in the same chair, at the same time, for what looks like an unremarkable day.

That will be exactly the point.

And I'll be right there with her, finally back on my own routine too.

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