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The Tiny Device That's Stopping Sundowning — On Day One By Tauna Young, FNP-CI want to be careful about how I write this...
09/11/2026

The Tiny Device That's Stopping Sundowning — On Day One

By Tauna Young, FNP-C

I want to be careful about how I write this, because I'm a clinician and I know the difference between an observation and a clinical trial. What I'm about to share is not a clinical trial. It's what I'm watching happen, in real time, in a real assisted living setting, with real residents.

And it is surprising me.

A Little Background

Recently, I approached The Cottages — a group of assisted living and memory care facilities across southwest Idaho that has been serving families in the region since 2001 — about participating in a small pilot study. The question: could CES, the FDA-cleared device known to significantly improve anxiety and insomnia — make a meaningful difference for residents who experience sundowning?

Sundowning is the pattern of increased agitation, confusion, and anxiety that occurs in the late afternoon and evening hours in people with dementia. The science behind it is well-understood: the brain's internal clock degenerates, melatonin production falls, and the nervous system gets stuck in a state of alarm it can no longer turn off on its own. What has been far less clear is what to do about it. Antipsychotics are the most common pharmaceutical tool, but they carry serious risks in elderly patients — increased falls, stroke risk, and accelerated cognitive decline. Clinical guidelines say to avoid them if possible. The problem is that "if possible" has always meant: if you have something else that works. For a long time, there hasn't been much else.

That's the gap I was dying to explore.

Shocking Results I Wasn't Ready For

The administrators at several Cottages locations agreed to participate — and so did the families of the residents involved, each of whom gave their permission before anyone's loved one was included. It would have been easy for all of them to say no. They said yes because they saw the potential for their residents to feel better in the evenings — and that reflects something I've observed firsthand about The Cottages: the people who work there bring a genuine love for their residents to work with them every day. This isn't just a job for them. You can see it in how they talk about the people in their care, and in the fact that when something came along that might make their residents' evenings easier, they didn't hesitate.

We've been at this for just a couple of weeks now. I want to be precise, because precision matters more than enthusiasm: I am seeing things I did not expect to see this quickly.

Several residents who were regularly needing PRN medications — as-needed doses of anti-anxiety drugs like Ativan — in the evenings are no longer needing them. Not because anyone decided to stop giving them. Because the evenings are different now. The need simply isn't there.

What surprised me most is how fast the change has happened. Staff are telling me consistently that sundowning symptoms stop on DAY ONE. Not after several weeks of adjustment. Day one. I did not anticipate that. I don't think anyone did.
Residents who previously paced, repeated the same questions, resisted care, and visibly suffered through their evenings are now, in the evenings, just themselves. Cooperative. Reachable. Present. That phrase keeps coming up. They're just themselves. It sounds simple. If you have ever watched a person with dementia sundown, you know it is not simple at all. It is everything.

And then there is the sleep piece. Residents who were previously up at night — wandering, unable to settle — are simply going to bed. Normally. At night. The way people are supposed to.

A Tool Geriatric Care Has Been Missing

For the first month of the study, I prescribed CES twice daily — morning and early afternoon — plus PRN as needed. The twice-daily structure is intentional: a loading phase designed to give the brain the opportunity to establish a calmer baseline. After the first month, once daily is typically sufficient, though it can be used more often.

Something happened in several instances that the staff didn't see coming — though I'll admit it didn't surprise me.

Staff placed the device on residents who were already in the middle of significant agitation — not as prevention, but as a response to someone who was already upset, already distressed. It calmed them down. Right there, in the moment. Quickly.

And then something equally striking: for residents who frequently resist taking their medications — a genuinely difficult challenge in memory care — staff found they could place the device, step out, and return twenty minutes later to a completely different interaction. The same resident who would have refused or become combative was now calm, cooperative, and reachable. The medication was passed peacefully. No struggle.

I noticed something in the way the staff were talking about this. They weren't just observing that their residents were doing better — they were experiencing something themselves: their jobs actually became easier. That matters more than it might sound. Caregiver burnout in memory care is real and well-documented, and anything that makes this work more sustainable is not a minor benefit.

None of this surprised me. I've seen CES work in real time with patients experiencing acute anxiety in my own psychiatric practice — the mechanism isn't mysterious. CES stimulates the nervous system toward a parasympathetic state, and that shift can happen quickly. I knew it could work this way. And now the caregiving staff at The Cottages has seen it too, in real time, with their own residents.

But watching it work that way in a dementia resident is significant in a different way. Because the alternative, at that moment, is a phone call to a prescriber. It is Ativan, or Haldol. Sedatives that carry real risk in an aging body — fall risk, respiratory risk, compounded cognitive effects in a brain that is already struggling.
Polypharmacy in elderly patients is already a serious concern. Every medication added to an aging person's regimen carries weight — interactions, side effects, the cumulative burden on a system that doesn't metabolize the way it did at forty. Geriatric clinicians have spent decades trying to reduce the medication load on elderly patients, not add to it.

The idea that you can simply place a small, non-pharmaceutical device on someone's earlobes in the middle of real distress and have it actually help, without sedating them, without altering their cognition further, without a phone call to a prescriber or a drug interaction to worry about — that is not a small thing. It is exactly the kind of tool that geriatric care has been missing.

Why I'm Writing About This Now

I'm writing now, while the study is still young and the data still coming in, because I think the caregiving community needs to know that something HUGE is happening here — even before the formal analysis is done.

I want to be honest about the limits of what I can say. This is a pilot. The sample is small. There is no randomized control group. This is how science works at the early stage: you watch, you document carefully, and you hold your excitement with both hands so it doesn't run ahead of the evidence.

What I can say with confidence is this: I am a clinician with more than a decade of hands-on experience, and I know what before and after looks like. What the staff are describing is consistent, specific, and clinically meaningful. These are not vague impressions — they are concrete, observable changes in behavior, medication use, and sleep patterns, reported independently across multiple residents and multiple locations.

In conversations with leadership from other long-term care and skilled nursing facilities in the region, I've found that the moment I describe what we're observing, the response is immediate — recognition of a problem they know intimately, and a potential solution they hadn't considered. There is genuine interest. Urgency, even.

The elderly population in long-term care may be one of the most overlooked potential beneficiaries of CES. A technology studied and used for over fifty years, and somehow the people who stand to benefit most — people for whom every additional medication carries real risk, people whose difficult evenings have simply been accepted as part of the disease — were largely left out of the conversation. We are in the early stages of changing that.

What It Means If This Holds

Sundowning affects up to 66% of people with Alzheimer's disease and is one of the primary reasons families transition a loved one into memory care. It is one of the biggest drivers of caregiver burnout. It is a daily source of suffering for people who have no ability to explain or control what their brain is doing to them in the evening.

If CES can interrupt that pattern — gently, without sedation, without drug interactions, without adding any pharmacological burden to a population already managing multiple medications — that is potentially a very large thing.

No published research has yet sought FDA clearance for CES specifically for sundowning. That's exactly why we're doing this. The science behind why it should work is sound: CES increases serotonin and melatonin production, reduces cortisol, promotes parasympathetic nervous system dominance, and modulates the circadian brain regions that degenerate in dementia. The biological drivers of sundowning and the documented effects of CES map onto each other with a precision that made me believe this was worth studying. What I'm watching in these first weeks is results which are more compelling than I even hoped.
I'll share more as the data comes in. In the meantime, if you are a caregiver navigating sundowning, or a memory care administrator looking for something beyond what the pharmaceutical toolkit currently offers — this is worth paying attention to — you can learn more about CES and sundowning here. https://program.neurovanacalm.com/dementia-sundowning/

More soon.

Tauna Young, FNP-C is the Founder & CEO of Neurovana and the owner of Harmony Mental Health in Boise, Idaho. The observations described in this post reflect early, preliminary findings from an ongoing pilot study and do not constitute clinical claims. Calm Ultra CES is FDA-cleared for anxiety and insomnia

Learn how Calm Ultra CES, FDA-cleared for anxiety and insomnia, may support caregivers exploring a gentle, drug-free approach to sundowning.

What CES And My Grandmother's Couch Taught Me About Dementia CareWritten by Tauna Young, Founder & CEO of Neurovana My g...
08/02/2026

What CES And My Grandmother's Couch Taught Me About Dementia Care

Written by Tauna Young, Founder & CEO of Neurovana

My grandmother taught me to crochet when I was seven years old. That was 45 years ago, and in the time since, crochet has become something close to a second language for me. It's a way of working through hard things with my hands when words weren't enough. I've always called it my therapist. It's the thing I turn to when life gets loud.

When her dementia progressed and she moved in with my uncle, her couch didn't go with her. I couldn't let it disappear, so I crocheted the whole thing, cover to cover, and did a photo shoot with her sitting on it. It felt like the right way to hold onto her, and onto what she did for me.

The couch is a tribute. This post is too.

My grandmother is 101 now. Along with memory loss, she's developed anxiety rooted in things that aren't real. She'll become convinced my mother, her own daughter, has died. (My mother is alive and well). She'll grow distressed over piano music she believes my mother is supposed to return, though she hasn't owned a piano in years. These beliefs feel completely real to her.

You can't reason someone out of a fear like that. It just has to be managed, gently, moment by moment.

A while back, my aunt (her caregiver) tried a Neurovana CES device on my grandmother during one of these stressful moments. What she noticed surprised her: my grandmother became calm.

CES is a small, FDA-cleared device that delivers a very mild current through earlobe clips, nowhere close to something like ECT. Most people feel nothing more than a tingle.

I'll be honest about the research: CES-specific studies on dementia agitation are still early. What exists is encouraging, but it's not a mountain of trials. What is well-established is CES's FDA clearance for anxiety, backed by large, independent studies. And here's why that matters: the brain's stress response doesn't file "dementia-related fear" and "anxiety" into separate folders. It's still the same limbic system, the same fight-or-flight circuitry, doing the work.

That distinction matters in dementia care, where agitation is so often managed with sedatives or antipsychotics, medications with real fall and cognitive risks for older adults. CES isn't a medication. No pill, no drug interactions, no sedation, no more fall risk. My grandmother isn't foggy or sedated by CES. She's just calm.

My grandmother's experience is just one family's story, not a clinical trial. But if your family is navigating this too, I know how much it can mean to hear when something helped somebody else's grandmother.

No adverse event has ever been reported across our device's 21-year history. And we offer a 30 day money back guarantee, so there's no risk in trying.

Learn more at neurovanacalm.com.

If you have a parent, spouse, or loved one with dementia, you’ve probably run into this: agitation, “sundowning” in the ...
08/01/2026

If you have a parent, spouse, or loved one with dementia, you’ve probably run into this: agitation, “sundowning” in the evening, trouble sleeping — and the main tools we reach for are medications that come with real risks for older adults. Oversedation. Falls. Drug interactions. We know this, and yet gentler options rarely come up in the conversation.
I want to tell you about one that should: Cranial Electrotherapy Stimulation, or CES.
It’s a small, FDA-cleared device that delivers a very mild electrical current through soft clips on the earlobes. To put “mild” in perspective — it’s nowhere close to something like ECT, which uses much stronger current and requires anesthesia. This is more like a whisper by comparison. Most people don’t feel more than a light tingle.
Here’s what the research shows so far, specifically in this population:
→ A study of institutionalized elderly patients with a type of dementia found nurses reported substantial improvements in behavior and sleep after just two weeks of use.
→ A study of spousal caregivers of Alzheimer’s patients found it meaningfully helped people fall asleep faster.
→ And across broader safety data, most users report no side effects at all.
I want to be honest with you: this isn’t a cure, and the research specific to dementia is still early and based on small studies. But when the usual choices are either “do nothing” or “accept the risks of sedating medication,” a gentle, well-tolerated non-drug option with promising early results should be part of the conversation.
This is exactly why I started Neurovana — to help families and care facilities learn about options they likely haven’t been offered.
CES is FDA-cleared and requires a prescription. If this is something you’re navigating for a loved one, or you work at a facility and want to learn more, let’s talk.

- Tauna Young, Founder and CEO

I’m grateful for the opportunity to join so many podcasts to talk about mental health, anxiety, and the nervous system.T...
07/09/2026

I’m grateful for the opportunity to join so many podcasts to talk about mental health, anxiety, and the nervous system.

This conversation was especially meaningful because it gave us the chance to explore the often unseen experience of caregivers—the emotional weight they carry, the impact it has on their own nervous systems, and why caring for the caregiver matters too.

Thank you to for inviting me to be part of such a thoughtful conversation. I hope it encourages caregivers to extend the same compassion to themselves that they so freely give to others.

🎧 I’d love to hear what resonated with you most after you listen.

Anxiety and insomnia after a hospital day can be a nervous system r...

We are excited to share that our CEO, Tauna Young, will be featured on SwagHer Magazine’s CEO Chatter LIVE on June 18!Tu...
06/15/2026

We are excited to share that our CEO, Tauna Young, will be featured on SwagHer Magazine’s CEO Chatter LIVE on June 18!

Tune in as Tauna discusses mental health, nervous system regulation, entrepreneurship, and the mission behind Neurovana.

📆 - June 18, 2026
⏰ - 7:30 PM EST
📍- Live on SwagHer Magazine’s Facebook, YouTube, and LinkedIn, and right here on our Instagram!

The official details are here.Neurovana Calm is coming to My Mind Is My Business™ 2026 in collaboration with LaKisha Mos...
05/13/2026

The official details are here.

Neurovana Calm is coming to My Mind Is My Business™ 2026 in collaboration with LaKisha Mosley, with our founder Tauna Young representing us and speaking at the event.

And we’re bringing the Neurovana Calm Corner to Houston.

This experience was created as a softer space to pause, breathe, reset, and reconnect with yourself during the event. Attendees will be able to visit the Calm Corner, experience the Neurovana Calm Ultra CES device, and enter the Calm Corner Giveaway.

Giveaway prizes include:

1 Neurovana Calm Ultra CES device
6 Calm Corner prizes

We’re honored to be part of this year’s MMIMB experience and cannot wait to share a deeper kind of reset with this community.

Join us on May 23, 2026 in Houston, TX.

Get tickets at mymindismybusiness.com

Your softer reset is waiting.

05/13/2026
05/13/2026
05/13/2026

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