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Memory Care

For us, caring for someone with dementia isn't a special case. It's part of the daily work.

Memory fading. Losing track of time or place. Sharp words that come out of anxiety. These are things we meet, day in and day out. So we don't panic. What may feel overwhelming to a family facing dementia for the first time is, for us, a road we've walked alongside many families before.

Why we involve more than one caregiver

When families come to us for dementia care, we often hear the same request: 'If possible, we'd like just one person.' The thinking is that a familiar face will put their parent at ease — and we understand that instinct completely.

But we deliberately involve several caregivers. There are two reasons.

The first is time. Dementia care unfolds over years. And when care begins, symptoms are usually at their mildest. From here, the care your loved one needs will gradually grow. Introducing a new person at that later stage — when things are already harder — asks a great deal of them. Becoming familiar with several faces now, while things are still calm, is how we prepare for what's ahead.

The second is fit. Long before dementia enters the picture, people simply click with some and not with others. When several caregivers are involved, there is often one your loved one opens up to in a way no one expected. Deciding on a single person at the outset closes the door on that possibility.

The first month is for learning

The first month of care is, for us, a crucial time to learn.Which symptoms appear, and when. Which hours of the day are calmest. Which subjects, or which songs, soften an expression. Which caregiver they're most comfortable with.We observe closely, write it down, and share it across the team. Only by building this picture does the right shape of care come into view. Put another way: there is no shortcut to good care that skips this time.

Confusion, or firm refusal, in those first few visits is not unusual. It isn't failure. More often than not, it's simply part of the road.

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Home and residential care serve different roles

We believe in keeping people in their own homes for as long as it works — because home is where your loved one feels safest.

In Hawaii, care homes with Japanese-speaking staff are rare. And in a residential setting, where one staff member looks after many residents, care shaped around one individual becomes difficult. The cost, too, is considerable.

That's why the order matters. Home for as long as home is possible — and a move to residential care when it's genuinely clear that home can no longer support them. Giving up on care at home too early narrows what's available for all the years that follow.

There are times we say no

At the same time, we can't take on every situation.

When physical assistance becomes so extensive that safety at home can no longer be maintained. Or when a person's temperament and their dementia combine in a way that places too heavy a burden on the caregiver at their side. In situations like these, pressing on with the service serves neither your loved one nor our staff.

When we reach that point, we say so plainly, and we think through the next options with you. Being clear about what we cannot do is part of what we mean by honest care.

How we meet each person

There are things we hold to when we sit with someone living with dementia.

Don't correct. Don't contradict. Don't rush.

What deepens anxiety

'That's not right.'

'I already told you.'

What we say instead

'You'd like to see your husband, wouldn't you'

'It's alright'

​'That's not right.' 'I already told you.' Words like these only deepen the anxiety. We don't argue with the world your loved one is living in. We take in the feeling first, then walk with them, gently, toward somewhere they feel safe.

'You'd like to see your husband, wouldn't you' — meeting the feeling where it is. 'It's alright.' And then a cup of tea, a walk outside together, a favorite song — easing naturally toward something else.

When the urge to go outside is strong, we don't hold them back. A caregiver simply falls into step beside them, and they walk together. Every one of these small approaches is shared across the team, so that everyone meets them the same way.

A Client's Story

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From ' Please leave ' to ' Thank you, always '

When we first began care, she would refuse us the moment she saw a caregiver's face. 'Get out.' 'Don't come back.' Some days she stacked chairs against the inside of her door so we couldn't enter. The anxiety that came with her dementia made being surrounded by unfamiliar people a heavy burden.

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The first thing we changed was the idea that we should do more. We narrowed the number of caregivers, so the same familiar faces visited, little by little. On days she refused us, we didn't push — we waited quietly on a chair in the hallway. Keeping a respectful distance is a form of care, too. And we carefully recorded the small changes, day by day.

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At the same time, we searched for the 'doorways' that might ease her heart. A photo book of kimono. Showa-era children's songs. The name of her hometown station. Beanbags. A doll just the right size to hold. One by one, we added small moments that felt familiar and joyful to her.

 

A few weeks later, she began greeting her caregiver with a smile: 'Oh, hello there.' Six months on, she was doing exercises, winning prizes at bingo, holding a therapy dog close and nuzzling its cheek — smiles her family thought they would never see again.

 

We didn't do anything extraordinary. We simply stayed close to her pace and her life, without rushing, without forcing. This was the result of that, and nothing more.

If you're thinking about care for someone with memory loss,
we're glad to talk.
We'll listen to where your loved one is and what your family hopes for, and suggest what we can do.

© Holly Services Hawaii INC. All rights reserved.

Bilingual support available (English / Japanese)

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