Caring for someone with dementia means learning a new language — one where feelings matter more than facts. These are practical approaches that caregivers and professionals rely on. Tap a topic to open it.
Communicating with warmth
- Approach from the front, make eye contact, and say your name: “Hi Mom, it's Clay.”
- Use short, simple sentences. One question at a time, with choices: “Tea or juice?”
- Give time to answer. Don't finish their sentences unless they want help.
- Don't argue or correct. Being “right” rarely helps — calm does.
- Respond to the feeling behind the words: “You sound worried. I'm here.”
- Body language and tone matter more than words as dementia progresses.
Repeated questions
The person truly doesn't remember asking. Answer calmly each time, or try:
- Write the answer on a whiteboard: “Lunch with Anna is at 12:00.”
- Look for the worry underneath — repeated “When are we leaving?” may mean anxiety about being left.
- Redirect to an activity they enjoy.
- Step away for a moment if you need to. Your patience is a limited resource; that's human.
Late-day confusion (“sundowning”)
Many people become more confused, restless or upset in the late afternoon and evening.
- Keep a steady daily routine with activity and daylight in the morning.
- Limit naps and caffeine later in the day.
- Turn on lights before dusk; close curtains to reduce shadows.
- Plan calm, familiar activities for late afternoon — music, folding towels, a snack.
- Reduce noise and visitors in the evening.
- Use the Behavior Diary to spot patterns.
Agitation and anger
Agitation is often communication. Before assuming it's “the disease,” check for:
- Pain — teeth, joints, constipation, a urinary infection
- Basic needs — hunger, thirst, the toilet, being too hot or cold, tiredness
- Environment — noise, crowds, TV, too many choices
- Feeling rushed, corrected, or not in control
Stay calm, lower your voice, give space, and offer comfort or a distraction. If you or the person is in danger, get to safety and call 911. A sudden change in behavior can mean illness or delirium — call the doctor.
Wandering and getting lost
About 6 in 10 people with dementia will wander at some point, often at the same time of day or when looking for “home” or an old routine.
- Keep a recent photo and a list of places they might go.
- Use an ID bracelet or a GPS device.
- Tell trusted neighbors.
- Door chimes, alarms, or locks placed higher or lower than eye level can help.
- If they go missing, search the immediate area for no more than 15 minutes, then call 911 and say the person has dementia.
Bathing and dressing
- Keep the old routine — bath or shower, morning or evening.
- Warm the room first. Use a towel over the shoulders for privacy and warmth.
- A handheld shower head and a shower chair help. Many people fear running water overhead.
- A sponge bath on some days is fine.
- Lay out clothes in the order they go on. Limit choices to two.
- If they refuse, stop and try again later — or let someone else try.
Eating and drinking
- Offer water often — people with dementia may not notice thirst.
- Serve one or two foods at a time on a plain plate that contrasts with the food.
- Finger foods help when utensils become hard.
- Eat together; people often copy what you do.
- Coughing or choking while eating needs a doctor's review — ask about a swallowing assessment.
Sleep problems
- Daylight and activity in the morning; a regular bedtime routine.
- A night light and a clear path to the bathroom.
- Avoid alcohol and late caffeine.
- Ask the doctor before using any sleep medicine — many increase confusion and falls.
Seeing or hearing things; suspicion
- Don't argue about whether it's real. Respond to the feeling: “That sounds frightening. You're safe with me.”
- Check lighting, mirrors and TV, which can be misread.
- Missing items “stolen”? Keep spares of important things and learn their hiding places.
- Tell the doctor — hallucinations can be a sign of Lewy body dementia, infection, or medicine side effects.
Home safety
- Remove trip hazards, add grab bars and night lights.
- Lock away medicines, cleaning products, firearms, car keys and power tools.
- Knob covers or automatic shut-off devices for the stove.
- Set the water heater to 120°F or lower.
- Keep a list of emergency numbers by the phone.
Behavior Diary
Log what happened, what came before and what helped. The diary finds patterns you can share with the doctor.
Open the diary →Care Circle
Spread the tasks across the family, in one shareable link.
Build it →Sources
- NIA. Alzheimer's Caregiving: Managing Personality and Behavior Changes.
- NIA. Coping With Agitation, Aggression, and Sundowning.
- NIA. Coping With Alzheimer's Behaviors: Wandering and Getting Lost.
- NIA. Coping With Hallucinations, Delusions, and Paranoia.
- NIA. Managing Sleep Problems in Alzheimer's Disease.
Reviewed September 2026. Education only — not medical, legal or financial advice.