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Knowing When More Help Is Needed



One of the most difficult decisions families face after a dementia diagnosis is recognizing when their loved one needs more support than they are currently receiving.


Most caregivers do not wake up one morning and suddenly realize their loved one can no longer be left alone. Instead, they adapt little by little. They add reminders. They install door alarms. They call more often. They stop by the house a few extra times each week. They start helping with groceries, medications, appointments, and household tasks. Over time, those small adjustments become part of everyday life.


The challenge is that dementia continues progressing. Eventually, there comes a point where reminders, safety devices, and occasional check-ins are no longer solving the underlying problem.


Recognizing that point can help families make decisions before a crisis forces them to.


When Wandering Stops Being an Occasional Concern

Many people with dementia wander at some point during the disease process.

Sometimes it starts innocently enough. Your loved one takes a walk but becomes confused about how to get home. They leave the house looking for a family member. They decide they need to go to work despite being retired for years.

At first, families often respond with practical solutions. They install door alarms, place signs near exits, use tracking devices, or ask neighbors to keep an eye out.

These measures can be extremely helpful.


However, there is a difference between someone who might wander and someone who is actively trying to leave on a regular basis.


If your loved one is repeatedly leaving the home, attempting to leave at night, becoming lost despite familiar surroundings, or showing no understanding of the dangers involved, the concern shifts from monitoring to supervision.


A GPS tracker can tell you where someone is. It cannot stop them from walking into traffic, falling into a canal, becoming dehydrated in the Florida heat, or accepting a ride from a stranger. When wandering becomes frequent, unpredictable, or driven by fear and confusion, families often need to consider whether someone should be present more consistently.


For some, this means having family members rotate shifts. For others, it means hiring companion care, adult day services, or eventually exploring memory care options.



When Sundowning Becomes Dangerous

Many caregivers are familiar with sundowning. They notice increased confusion, restlessness, anxiety, or agitation later in the day. What is often overlooked is when sundowning begins creating actual safety concerns. A person who becomes mildly confused in the evening is very different from someone who attempts to leave the house at 10 PM because they believe they need to pick up their children from school.


You may notice your loved one packing bags, trying to drive, searching for deceased relatives, becoming frightened by shadows, or insisting they need to go somewhere immediately. In these situations, the goal is no longer simply calming them down.

The goal becomes preventing harm. On occasion, offering distractions like saying "Oh yeah, we got them earlier how about you come help me make them some food."


If evening behaviors are becoming severe, talk with their healthcare provider. Medication reviews, sleep evaluations, vision problems, pain, and untreated medical conditions can all worsen sundowning. Families may also need to adjust routines. Some people do better with fewer evening visitors, less television noise, more consistent lighting, and predictable nighttime schedules.


If these episodes are occurring regularly and no one is available to supervise during those hours, it may be time to consider additional support or respite services.


When You No Longer Feel Comfortable Leaving Them Alone

This is one of the clearest indicators that more help may be needed.

Ask yourself a simple question:

"If I needed to leave for four or five hours unexpectedly, would I feel comfortable doing so?"

Many caregivers find themselves hesitating. Not because their loved one cannot physically stay home, but because they are worried about what might happen while they are gone.

  • Would they remember to eat?

  • Would they take medication correctly?

  • Would they answer the door?

  • Would they know what to do if the smoke detector went off?

  • Would they become frightened and attempt to leave?

When you begin planning your day around making sure someone is never left alone, that is important information.


It does not automatically mean a nursing home is necessary. It does mean the current level of support may no longer match the person's needs. This is often when families begin exploring companion care services, adult day programs, or part-time in-home caregivers.


When Safety Awareness Starts Disappearing

Many people with dementia eventually lose the ability to recognize danger. This is very different from simply forgetting something.


You may notice your loved one walking outside barefoot, attempting to cook with damaged appliances, taking medications multiple times because they forgot they already took them, or opening the door to anyone who knocks. One family may discover their loved one gave their banking information to a scam caller. Another may find they left the stove on and went to bed.


These situations are often signs that the disease is affecting judgment, not just memory.

At this point, more reminders are rarely the solution. The issue is no longer remembering what to do. The issue is recognizing what is safe.


If you find yourself constantly fixing dangerous situations after they happen, it may be time to consider increasing supervision before something more serious occurs.


When Physical Care Needs Begin Increasing

As dementia progresses, many families find themselves managing more than memory loss.

Falls become more common. Mobility may decline. Incontinence may develop. Bathing, dressing, and toileting may require assistance.

This is often where caregiving becomes physically demanding.

An adult child may be able to remind a parent about medications, but helping someone safely transfer from a bed, recover after a fall, or manage incontinence several times a day requires a different level of care.

Many caregivers wait until they are injured or completely exhausted before asking for help.

If physical care needs are increasing, consider bringing in assistance sooner rather than later. Home health aides, personal care attendants, and respite caregivers can often provide support before the situation becomes overwhelming.



When the Caregiver Is Providing Constant Supervision

There is a difference between helping someone and monitoring them every waking moment. Many caregivers slowly move from being supportive family members to becoming full-time caretakers without realizing it.


You may find yourself checking cameras throughout the day, calling repeatedly to make sure your loved one is safe, sleeping lightly because you are afraid they will leave the house, or avoiding errands because you do not want them alone. At some point, your loved one's safety may depend entirely on your constant presence.


When that happens, it is worth asking whether the current arrangement is sustainable.

No single caregiver can provide twenty-four-hour supervision indefinitely without support.

This is often when respite care, overnight caregivers, adult day programs, or memory care communities become realistic options.


More Help Does Not Mean Failure

Many families resist additional support because it feels like giving up. However, getting help is often what allows families to continue providing care.


One of the hardest truths about dementia is that the disease changes over time. The strategies that worked six months ago may not work today, and the solutions that work today may not be enough a year from now.


The goal is not to remove your loved one from their home or take away their independence. The goal is to match the level of support to the level of need.


The right answer is the one that keeps your loved one safe while also allowing you to remain healthy enough to continue supporting them.


When you are ready to take the next step, feel free to check out Top 10 Signs It’s Time for Assisted Living: A Guide for Families. If you are not at that stage, please feel free to check out our Caregiver Resources for more support with your loved one.

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