In this article
“Mum, lift your arm. A little more. That’s it.”
It is half past seven in the morning. A daughter holds a flannel in one hand and supports her mother’s elbow with the other, so she won’t sway on the stool in the bathroom. Her mother looks out of the window as if she weren’t there. Both of them act as though this were a perfectly ordinary morning. Half an hour later, in the car on her way to work, the daughter suddenly starts crying and doesn’t quite know why. Nothing bad happened. Mum was kind. Everything went to plan.
And yet something did happen. The woman who once washed her hair and taught her to tie her shoelaces now depends on her hands. That shift is not only practical. It is a shift in the relationship, and neither of them had words for it when they agreed that Mum would “stay at home for now”.
That is what this piece is about: not how to organise care, but what caring for a parent at home does to the relationship between you and your parent — and to the family around you.
A home that turns into a sickroom
When care moves home, the space changes. There is a bed with side rails in the living room, a pill organiser sorted by days on the kitchen table, grab rails in the bathroom. A home that was a place of privacy and habit becomes a workplace. The parent is often the first to feel it: in their own house they are no longer entirely in charge. And you are there every day — no longer as a guest or a child visiting, but as someone with a job to do.
Most care for older people across Europe does not happen in institutions but at home, in the hands of those close to them. This has a great deal going for it: a familiar place, one’s own things, a sense that life goes on. But it also has a cost, and research has been measuring it for a long time. In a well-known American study by Richard Schulz and Scott Beach, older people who were caring for an ill spouse and experienced that care as a strain had a 63% higher risk of death over four years than peers who were not caregivers. These were spouses, not adult children, but the message holds more broadly: the long-term strain on a carer is not a side issue.
This piece, however, is not about exhaustion. I am interested in something quieter: how what you and your parent are to each other changes through care.
Your parent’s body in your hands
The hardest moments in care often don’t come with the big decisions but with everyday tasks. Help with washing. Help on the toilet. Changing underwear. Cutting toenails. These are things that, as adults, we usually do ourselves or entrust only to a partner or to healthcare staff. When a child starts doing them, something happens for which the family has no ready language.
In parents, this often awakens shame — not necessarily spoken. It shows up as silence, an averted gaze, excessive politeness (“sorry to put you through this”), or the opposite: grumbling and refusing help. In adult children there is often embarrassment, sometimes disgust, which they then take as proof that they are bad people. None of it is proof of anything. In every family the body is marked by rules — what is shown, what isn’t mentioned, who may touch whom. Care turns those rules upside down overnight.
Dignity in care does not lie in the embarrassment never appearing, but in how you handle it. It helps to ask your parent how they would like something done. To let them do what they still can, even if more slowly. Not to wash them while others are present. And to say out loud, at least once, what is hard: “I know this isn’t easy for you. It isn’t entirely easy for me either. But I’m glad to do it for you.”
Old roles come back
In relational family therapy, in which I am training, we see the family as a system in which a change in one member changes the whole. When a parent falls ill and needs care, the system doesn’t reorganise from scratch. It reorganises along old tracks.
Care is often taken on by the child who was already “the reliable one” in childhood. The one who looked after the younger ones, who calmed the arguments, who noticed when Mum was struggling. Family therapists know this role well — I wrote about it in Roles in the family: the hero, the scapegoat, the invisible child. Which was yours? When a parent falls ill, the role is not just repeated, it gains official status. And because it was always taken for granted, often nobody notices it — not even the person carrying it.
Ivan Boszormenyi-Nagy used the term invisible loyalties for these unseen bonds. In every family there is an unspoken ledger: who gave what to whom, who owes whom, who was short-changed. Caring for a parent opens that ledger. One person cares because they “owe it”. Another cares because they hope to be seen at last. A third withdraws because they feel they paid too much long ago. None of these stances is simply good or bad — each has its own history.
If caring reminds you of something you know from very early on, it is worth noticing. It isn’t necessarily bad. But it may mean that you are not only caring for your parent as they are today, but also for the parent they were — and for yourself as you were back then. I described part of this shift in When a parent depends on you: the role reversal that isn’t.
Siblings: who is close and who is far
Almost every family with more than one child faces the same question when a parent needs care: why am I carrying more than the others? The answer is rarely just practical. It is true that someone lives closer, has a less demanding job or no small children. But underneath lie old stories — who was Mum’s favourite, who left early, who never got on with Dad.
Caring for a parent often revives old alliances between siblings — the ones I wrote about in Siblings, alliances and coalitions: the invisible geometry of the family. A sister who does the caring and a brother who comes on Sundays can talk about the same parent as if they were two different people. She sees the daily burden; he sees a mother who dresses up for lunch and is in good spirits. Both are right — and both feel misunderstood.
What to do when a brother or sister doesn’t help is a subject in its own right, with its own piece: When your brother or sister won’t help care for your parents. Here I would stress just one thing: conflict between siblings over care is almost never just a conflict about the rota. It is a conflict about who meant what to whom in the family. That is why a table of divided days rarely resolves it, unless what lies beneath it is talked about.
Anger and tenderness in the same room
People who care for a parent often admit something they are ashamed of: that they are angry. At the parent, for refusing help, for being ungrateful, for repeating themselves. At themselves, for being angry. And at the same time they love them, are grateful for what they did, and dread the day when they will no longer be there.
We call this double feeling ambivalence. In care it is almost the rule. It is not a sign that you are a bad child, but a sign that the relationship is real — that everything accumulated over decades lives in it. Anger only becomes dangerous when it piles up silently with nowhere to go. Then it erupts over something trivial, or turns inwards and becomes guilt.
This is how it sometimes sounds (a composite conversation, not a real person):
“That’s the third time today you’ve asked whether I locked the door.”
“I’m only asking.”
“I know. Sorry. I’m tired.”
Silence. “You’re more the mother here now than I am.”
“No, Mum. You’re still my mum. I’m just helping you with my hands.”
“But sometimes you’re scared, aren’t you?”
“Yes. Sometimes I am.”
Something important happens in this short exchange. The anger is spoken and quickly repaired. The mother names the shift both of them feel. The daughter doesn’t deny it but puts it in its proper place — I’m helping you, but I haven’t become your mother. And at the end they dare to name the fear. Moments like this don’t remove the burden, but they keep the relationship alive.
Trapped in the role
In the 1990s the sociologist Leonard Pearlin and his colleagues described a phenomenon they called role captivity: a carer’s sense of being in a role they did not choose and cannot leave. Alongside it they described loss of self — the gradual fading of other parts of one’s identity. You are no longer a friend, a partner, a colleague, someone with a hobby. You are the one who looks after Mum.
This loss affects not only you but also your relationship with your parent. When care is the only thing that connects you, conversation shrinks to medication, digestion and doctor’s appointments. Your parent loses the child they could talk to about books, politics or grandchildren. You lose a parent who was more than a patient. The paradox of care is that you are physically closer than ever, yet emotionally you can drift apart.
So it isn’t selfish to keep the parts of your life that have nothing to do with care. It isn’t selfish to sometimes spend an hour with your parent in which you do nothing useful — you just drink coffee, look at old photographs or listen to the radio. That hour is part of care, even if you won’t write it into any timetable.

Nor are boundaries coldness here. Boundaries in care mean knowing what you can give without disappearing in the process — and saying so to your parent, your siblings and yourself.
Exercise: an hour that isn’t care
If you are caring for a parent at home, try this during the week. It takes less time than you think.
- Write down everything you do for your parent on a typical day. Just list it — washing, medication, cooking, phone calls, lifts.
- Mark each item as either care or relationship. Care is what someone else could also do. Relationship is what only you can give.
- Count how much there is of each. If there is almost no relationship, that isn’t an accusation, it’s information.
- Choose one hour a week that will be relationship only. No chores. Ask your parent what they would like to do — or what they would like to tell you about the time when they were your age.
- Think about which care task you could hand over to someone else. A sibling, the community nursing service, home help. Not because you can’t cope, but so that you keep room for the hour in the previous step.
Where to find help
Caring at home is not a task you have to carry alone. In Slovenia the first point of contact is usually your parent’s GP, who can advise on treatment and aids and refer you onwards. The community nursing service (patronaža) at the local health centre visits patients at home and shows relatives many things they would otherwise learn through their own mistakes — from lifting to skin care. For social rights, home help and other forms of support, it is best to ask at the relevant social work centre (center za socialno delo). Conditions and options change, so it’s better to ask there than to rely on what someone heard from a neighbour.
It is also useful to draw who is around you. The Map of your support network tool can help. People who care often underestimate how much help would be available — because they have never asked for it.
And if you notice that caring is starting to wear down your own health — that you aren’t sleeping, that you cry often or no longer feel anything — go to your own GP too. Not just your parent’s.
When this doesn’t hold
I wouldn’t want to give the impression that caring at home always damages the relationship. It doesn’t.
Care can also deepen the relationship. As early as 1991, M. Powell Lawton and his colleagues showed that in carers burden and satisfaction do not exclude each other — the same person can experience care as hard and, at the same time, as meaningful. Many people experience, in caring for a parent, a tenderness that was missing in childhood for the first time, or finally hear stories the parent never told before. Some are reconciled with their parent precisely through care.
Not every difficulty in the relationship is caused by care. If the relationship was already difficult — because of violence, addiction, neglect — care does not create this but reveals it. In such cases it is worth seriously asking whether you are the right person for this task. The piece Adult children and parents: can the relationship still be repaired? looks at this.
Care at home is not always the best choice. When a parent needs constant supervision, when care is physically too demanding, or when the carer falls ill themselves, choosing a different form of care can be an act of care, not betrayal. Sometimes the relationship is preserved precisely because you stop being the carer and become, once again, the child who comes to visit.
And finally: this piece does not replace consultation with the doctor or the professionals looking after your parent’s health. Psychotherapy can help with what care does to the relationship and to you, not with decisions about treatment.
If you would like to talk about what is happening in your family with someone who isn’t part of it, that can also be a task for therapy. In relational family therapy we often look at exactly this: which old roles and loyalties care has awakened, and how to carry them without being buried by them. I also work with English-speaking clients in person in Ljubljana.
What to remember
- Caring at home changes not just the timetable but the relationship — body, decisions, time and conversation.
- Embarrassment, shame, anger and tenderness often come together in care. Ambivalence is not a sign that you are a bad child.
- Care awakens old roles and loyalties — between siblings too. A conflict about the rota is rarely just about the rota.
- Each week, keep at least one hour that isn’t care but relationship.
- The GP, the community nursing service and the social work centre are part of the team, not an admission of defeat.
Sources
- Schulz, R., & Beach, S. R. (1999). Caregiving as a risk factor for mortality: The Caregiver Health Effects Study. JAMA, 282(23), 2215–2219. PubMed
- Pearlin, L. I., Mullan, J. T., Semple, S. J., & Skaff, M. M. (1990). Caregiving and the stress process: An overview of concepts and their measures. The Gerontologist, 30(5), 583–594. PubMed
- Lawton, M. P., Moss, M., Kleban, M. H., Glicksman, A., & Rovine, M. (1991). A two-factor model of caregiving appraisal and psychological well-being. Journal of Gerontology, 46(4), P181–P189. PubMed
- Zarit, S. H., Reever, K. E., & Bach-Peterson, J. (1980). Relatives of the impaired elderly: Correlates of feelings of burden. The Gerontologist, 20(6), 649–655. PubMed
- Boszormenyi-Nagy, I., & Spark, G. M. (1973). Invisible Loyalties: Reciprocity in Intergenerational Family Therapy. New York: Harper & Row.
- Gostečnik, C. (2017). Relational Family Therapy: The Systemic, Interpersonal, and Intrapsychic Experience. New York: Routledge.
Is caring for your parent pulling you away from them — and from yourself?
Write to me. Together we can look at which old roles care has awakened and how to carry it without losing yourself.
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