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🎵 “Sundown” – EOA When the Sun Goes Down and Everything Changes (Gordon Lightfoot)

May 27
4 min read

Updated: Jul 12

🎵 “Sundown, you better take care…”

And honestly?


If you’re caring for someone with Alzheimer’s or dementia…

👉 7pm can feel like entering another dimension.


One minute things seem manageable.

Then:

  • The pacing starts

  • The agitation kicks in

  • The confusion increases

  • The refrigerator opens 17 times

  • The muttering begins

  • The anxiety rises

  • The wandering starts

  • The repetitive questions return


And you’re standing there exhausted thinking:

👉 “What just happened?”


Welcome to:

Sundowning

Sundown is pretty sometimes...
Sundown is pretty sometimes...

🧠 WHAT IS SUNDOWNING?


Sundowning is:

👉 Increased confusion, anxiety, agitation, restlessness, or behavioral changes occurring later in the day or evening.


Usually:👉 Late afternoon into nighttime


Many caregivers describe it as:

👉 “The switch flips around or after dinner time.”



🌙 WHAT DOES IT LOOK LIKE?

Every person is different, but common signs include:

✔️ Pacing

✔️ Wandering

✔️ Repetitive behaviors and words

✔️ Increased anxiety

✔️ Agitation or anger

✔️ Mumbling or word salad worsening

✔️ Looking for “home”

✔️ Confusion about time

✔️ Obsessive routines

✔️ Opening/closing cabinets or fridge repeatedly

✔️ Sleep refusal

✔️ Shadowing caregiver constantly (jump scare on some days, he's sneaky)


💔 WHAT IT LOOKED LIKE IN OUR HOUSE

For us:

👉 Around 6:30–7pm the energy changes completely.


You can almost feel it building.

He:

  • Wanders

  • Looks in the fridge repeatedly

  • Gets anxious if routine changes

  • Becomes hyper-focused on random things

  • Starts mumbling more

  • Communication worsens

  • Gets restless and unsettled

  • becomes agitated


And honestly?


👉 It can completely drain the caregiver by nighttime.



🧠 WHY DOES SUNDOWNING HAPPEN?

Doctors believe several things contribute:

  • Brain changes affecting body clock/circadian rhythm

  • Fatigue/exhaustion

  • Low lighting/shadows

  • Hunger/dehydration

  • Overstimulation during the day

  • Anxiety

  • Poor sleep patterns

  • Difficulty processing evening transitions


⚠️ WHAT STAGE DOES SUNDOWNING START?

It can appear:

👉 Earlier than people expect


But becomes more common in:

  • Mid-stage Alzheimer’s

  • Stage 4–6 typically


For many EOA spouses:

👉 Stage 5 is where it becomes VERY noticeable.


😔 WHY EVENINGS ARE SO HARD FOR CAREGIVERS

Because honestly?

👉 YOU are exhausted too by then.


You’ve already:

  • Managed the day

  • Cooked

  • Redirected behaviors

  • Worked

  • Cleaned

  • Monitored medications

  • Repeated yourself 100 times

Then just when YOU are empty:

👉 Sundown starts.


💡 WHAT HELPED US MOST

Not curing it.

Just:

👉 Reducing the chaos around it.


✔️ KEEP ROUTINE VERY PREDICTABLE (Cue up the movie-- Rain Man to remember how real this is now)


This matters HUGE.

Dinner:

👉 Same time


Showers:

👉 Same routine


TV:

👉 Familiar shows


Lighting:

👉 Consistent


Unexpected evening plans?

👉 Usually bad idea for us now.


✔️ REDUCE STIMULATION

Evenings are NOT the time for:

  • Big crowds

  • Loud restaurants

  • Long outings

  • Complicated social events


Too much stimulation earlier in the day often means:

👉 Worse evenings.



✔️ IMPROVE LIGHTING

Shadows can increase confusion/anxiety.

We found:

👉 Warm lighting helps a LOT. (All my bulbs are now "soft"


✔️ LIMIT LATE CAFFEINE & SUGAR

Especially if anxiety/agitation already exists.


✔️ AFTERNOON REST HELPS

Missing naps or downtime?

👉 HUGE trigger for us.


✔️ PHYSICAL ACTIVITY EARLIER IN THE DAY


Walking.

Biking.

Exercise.


Helps burn off:

👉 Restless energy.


⚠️ SAFETY ISSUES DURING SUNDOWNING

This part matters.

Sundowning increases risk for:

  • Wandering

  • Falls

  • Aggression

  • Leaving the house

  • Medication confusion

  • Kitchen accidents

  • Urinating in weird places


💡 THINGS TO CONSIDER

✔️ Door alarms

✔️ Cameras

✔️ Medical ID bracelet

✔️ Night lights

✔️ Simplified evening routines

✔️ Camera's on in house

✔️ Locks like "Kwickset" that notify you when a door to outside opens.

Kwickset Halo Lock (Aura works too) https://a.co/d/056jpa1P


💊 CAN MEDICATION HELP?

Sometimes yes.

But this is VERY individualized.


🩺 TALK TO YOUR DOCTOR ABOUT:

  • Increased evening agitation

  • Anxiety

  • Sleep disruption

  • Wandering

  • Aggression

  • Hallucinations/paranoia


💊 MEDICATIONS DOCTORS MAY DISCUSS

Depending on symptoms:

  • Anxiety medications

  • Sleep medications

  • Antidepressants

  • Medication timing adjustments

  • Dementia medications


⚠️ IMPORTANT

Some medications can:

👉 WORSEN confusion or increase fall risk


So NEVER self-adjust without guidance.


🧠 WHEN TO SEEK MEDICAL HELP QUICKLY


Call doctor sooner if you notice:

  • Sudden severe behavior changes

  • Hallucinations

  • Aggression

  • New wandering

  • Major sleep changes

  • Rapid confusion increase

Because infections, medication changes, dehydration, or other illnesses can worsen symptoms FAST.


📚 GOOD RESOURCES

National Institute on Aging – Sundowning & Alzheimer’s



💔 THE HARDEST PART

Sometimes your spouse:

👉 Truly cannot settle


And no matter what you try:

  • The pacing continues

  • The anxiety continues

  • The questions continue


And caregivers end up:

👉 Completely emotionally depleted by nighttime.



🧠 WHAT I’VE LEARNED

Sundowning is not:

❌ Them being difficult

❌ Intentional behavior

❌ Bad attitude


It’s:👉 Brain fatigue and neurological change


🎵 Why “Sundown”

Because every caregiver eventually recognizes:

👉 The sun going down changes everything.


And evenings become something you mentally prepare for every single day.


💭 Final Thought

If evenings feel impossible sometimes:

👉 You are not failing.

Sundowning is one of the most exhausting parts of dementia caregiving.


Routine.

Patience.

Medical support.

And sometimes simply surviving the evening one hour at a time…

That’s enough.


💬 Disclaimer

 I’m not a doctor, lawyer, therapist, or expert—just a wife trying to figure this out one day at a time. Everything shared here is based on our experience and things that have helped us along the way. Take what helps, leave what doesn’t, and always check with professionals when needed. I also use AI to help clean up my writing, organize thoughts, and pull together resources because honestly… caregiver brains are tired too. If something here helps another family feel less alone, then it’s worth sharing.




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