FROM KAT

Should I take my mom's phone away? A daughter's honest answer

Kat, founder of Everline

5 min read

Almost every caregiver forum answers this the same way: take the phone. Hide it, suspend the plan, tell her it is broken. I have read that thread a hundred times, and I want to give you the answer I wish someone had given me, which is that the advice is sometimes exactly right and sometimes exactly wrong, and the difference is knowable.

My mother has dementia and lives in a care facility. On her worst days she calls me fifty times, and she calls my siblings, and my cousin, and anyone else whose number still works. So I am not writing this from the outside.

First, the honest case for taking it away

I am not going to pretend this is always the wrong call. Take the phone, or lock it down hard, when:

She is calling 911 repeatedly. This is the most common reason facilities ask families to remove a phone, and it is a good reason. Emergency lines are a shared resource, and repeated false calls can end with responders who stop hurrying.

Money is involved. If she is giving card numbers to people who call, or wiring money to someone she believes is a grandchild, the phone has stopped being a comfort and become a door. Act quickly here.

She is calling strangers, or people who have asked her to stop. Old numbers, wrong numbers, an ex-husband, a workplace from thirty years ago. This distresses her too, not just them.

The calls are frightening her more than they settle her. Some people with dementia get more agitated on the phone, not less, especially later in the day. If every call ends worse than it started, the phone is not doing the job you think it is.

If any of those describe your situation, take the phone and do not spend one minute feeling guilty. You are protecting her.

The question almost nobody asks first

Here is the distinction that changed how our family handled this. There are two completely different problems that look identical from the outside, and the same solution cannot fix both.

A safety problem points outward. She is reaching people who should not be reached, at hours that cause harm, about things that can cost her money or dignity. The calls are the danger.

A comfort problem points inward, at the same two or three people, over and over. She calls, hears your voice, settles for a few minutes, and then the memory of the call dissolves while the worry underneath it stays exactly where it was. So the fear rises again, whole and fresh, and she reaches for the thing that worked. To her, every call is the first call. She genuinely cannot count them.

If it is a comfort problem, taking the phone away does not solve it. It ends your ringing, which is not nothing, and I understand why exhausted people reach for it. But the fear that was driving the calls is still there and still unanswered, and it has to go somewhere. In our experience and in most accounts I have read, it goes to whoever is nearest: the nurses, the aides, the woman in the next room, the front desk. Families are often told a few weeks later that she is anxious all day and following staff around.

For someone whose main remaining comfort was hearing a familiar voice, losing the phone can feel like the family disappeared. She will not remember that you visited on Sunday. She will feel that she cannot reach anyone.

What to do when it is a comfort problem

Narrow the phone instead of removing it.

Limit who she can reach. Call-limiting phone services built for dementia can block repeat dialing, switch off calls after a certain hour, and stop unknown numbers, while leaving the people she loves reachable. This is the middle path few families hear about, and it addresses the safety half without taking away the comfort half.

Simplify the phone itself. A handset with a few large photo buttons is easier than a smartphone she can no longer navigate, and it quietly removes the ability to dial randomly.

Share the ringing. Before buying anything, ask the family. Even two more people taking a window each changes the arithmetic. It is free, and it is the first thing worth trying.

Make sure the numbers that remain actually answer. This is the part that gets left out. A ring that ends in voicemail deepens the fear that started the call, and a frightened person who cannot reach anyone will try again immediately. Whatever else you do, the small set of numbers she can still reach should be answered warmly, every time, by someone who is not exhausted.

That last one is the one our family could not solve with effort, because there is no amount of love that makes one working person available fifty times a day. It is why I ended up building Everline, which answers her calls in my own recorded voice when I cannot pick up. I am telling you that because it is the honest end of my story, not because it is the answer for you. If you want the whole field laid out, including the options that are nothing to do with us, we wrote an honest comparison of what a family can actually do.

What I would say to you if we were sitting together

You are allowed to want the ringing to stop. That is not the same as wanting her to stop needing you, and the guilt that follows the wish is not evidence of anything except that you love her and you are tired.

Ask what the calls are for. If they are reaching outward toward danger, limit them without apology. If they are reaching inward toward you, the goal is not fewer calls. It is that the reaching lands somewhere soft, more often than you alone can manage.

Both of those are good caregiving. Only one of them is served by taking the phone.

Questions families ask

Should I take my mom's phone away if she has dementia?

It depends what the calls are doing. If she is calling 911 repeatedly, giving money to strangers, or dialing people at 3am, that is a safety problem and the phone may genuinely have to go. If she is calling the same two or three people for reassurance, that is a comfort problem, and taking the phone removes her comfort without touching the fear underneath it. The reaching usually moves to the nurses and the neighbors instead.

Is it cruel to take a phone away from someone with dementia?

No. Families who do it are almost always protecting someone, and it is often the facility or a doctor who suggests it. What is worth avoiding is doing it as a first move, before anyone has asked what the calls are for. Cruelty is not the risk here; acting without asking that question is.

What are the alternatives to taking a dementia parent's phone away?

Limiting the phone rather than removing it. A call-limiting phone service can block repeat dialing, late-night calls, and unknown numbers while leaving family reachable. A simple phone with a handful of photo buttons narrows the world without emptying it. And whatever numbers remain should actually answer, because a ring that ends in silence deepens the fear that started the call.

My mom calls me 30 times a day. Am I a bad daughter for wanting it to stop?

No. Wanting the ringing to stop is not the same as wanting her to stop needing you. One person cannot answer what a care team answers in shifts, and being worn down by it is arithmetic, not a character flaw.

How do I know if the calls are a safety problem or a comfort problem?

Look at who she is calling and what she wants. Comfort calls go to the same small handful of people, ask the same reassuring questions, and settle for a few minutes after she hears a familiar voice. Safety calls go outward, to 911, to strangers, to numbers she does not know, or they involve money. Comfort calls need answering. Safety calls need limiting.

If the phone calls are the hard part, this is what I built.