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Families & caregivers · Cancer

When a parent has cancer: activities, resources, and concrete arrangements to implement

When a parent has cancer, a child's daily life is reorganized unexpectedly around appointments, fatigue, and silences. This article gathers activities, resources, and concrete tools to implement when a parent has cancer, to help the child understand, express what they feel, and maintain stable references. None of this requires specialized materials: a notebook, some markers, a box, a little time.

  • ⏱️ 19 min read
  • 👥 For families and caregivers
  • 🔄 Updated in August 2026

Dans cet article

La formation associée

Formation QualiopiQuand un parent a un cancer : accompagner ses enfants face à la maladieDécouvrir la formation →

It's a toolbox, not a treatise on psychology. Fourteen activities described clearly enough to be launched tonight, a daily and weekly organization, the arrangement of the child's spaces, and free resources to print. The goal is never performance: it is to maintain a living connection between the child and their parent, and to give the child simple ways to express what they are going through.

The essentials in 30 seconds

Supporting a child during a parent's illness is based on three principles: true words, stable references, preserved connection. A child needs to understand what is happening, at their level, more than to be protected from reality.

  • Name — using simple and honest words about the illness calms more than silence, which allows the imagination to do the worst.
  • Rhythm — keeping known rituals (meals, bedtime, school) gives the child a foundation that does not change when everything else does.
  • Connect — preserving moments with the sick parent, even very short ones, matters more than their duration.
  • Express — drawing, question box, emotions jar: providing a channel for what is not yet expressed in words.
  • Identify — knowing the signs that should lead to a doctor or psychologist, without dramatizing or trivializing.

4 rules before proposing activities when a parent has cancer

Before choosing an activity, a few principles apply to all. They avoid the most common awkwardness and make the proposals easier for the child to accept, regardless of their age.

🗣️

Speak the truth, at the child's level

Use the word “cancer” rather than an anxiety-inducing vagueness, with short phrases appropriate for the age. Lies protect less than measured truth.

🔁

Propose, never force

Open a door, don’t push through it. A child who refuses today may accept tomorrow: the invitation remains open, without reproach.

⏱️

Short and regular

Ten attentive and available minutes are better than an hour of distraction. The regularity of a small ritual reassures more than a large isolated moment.

👂

Follow the child

Answer their questions when they ask, without anticipating or revealing everything. They set the pace for what they can hear.

⚠️ Some signs should lead to a professional

These activities support daily life, they do not replace any follow-up. If the child shows lasting sleep disorders, marked withdrawal, a drop in school results, repeated pains without cause, unusual aggression, or dark thoughts, talk to the treating physician, school medicine, or a psychologist. In case of immediate danger, contact your country's emergency services without delay. Asking for help is never a failure: it is often the best gift you can give to a child.

Talking about the illness and naming emotions

A child feels everything, even what we think we are hiding from them: whispers in the kitchen, red eyes, sudden appointments. What they do not understand, they invent, and their imagination is often more frightening than reality. These four activities provide a channel for what is not yet expressed in words.

✅ To say
  • “ Dad/Mom has an illness called cancer. The doctors are taking care of it with strong medications. ”
  • “ It’s not your fault, and it’s not contagious: you can’t catch it by hugging. ”
  • “ You have the right to be angry, sad, or even to laugh and play. All your emotions have the right to be there. ”
  • “ If you have a question, you can ask me. If I don’t know, I will tell you. ”
❌ To avoid
  • “ Nothing is happening, everything is fine ” — the child feels the opposite and stops trusting you.
  • “ You are the little man of the house now ” — this phrase places a weight on their shoulders that is not theirs.
  • Vague metaphors (“ he is gone ”, “ he is sleeping ”) that confuse instead of explain.
  • Promises you cannot control (“ he will heal, for sure ”).
1

The jar of emotions

  • Objective — to give a word and an image to what the child feels when they do not yet have the phrases to express it.
  • Materials and duration — a transparent jar, tokens or colored marbles associated with emotions (yellow = joy, blue = sadness, red = anger, green = calm, gray = fear), 5 minutes each evening.
  • Procedure — each evening, the child puts in the jar the color(s) of their day. We look together, without judging, and simply name: “ lots of blue today ”.
  • Easier (small) — only two colors, joy and sadness, with drawn faces.
  • Harder (big) — write a word on a folded paper next to the token to explain why.
  • Sign that it works — the child spontaneously goes to the jar, or comments on the colors without being asked.
2

The free drawing of what is happening

  • Objective — to let out through the pencil what is not expressed in words: fear, the hospital, family.
  • Materials and duration — sheets, markers, colored pencils, 10 to 15 minutes.
  • Procedure — suggest without instruction: “ you draw what you want ”. We sit next to them, draw ourselves, and do not comment on the content. If the child explains, we listen without correcting.
  • Easier — draw together a neutral theme, the house, the family.
  • Harder — suggest “ draw how you feel today ” and then talk about it.
  • Sign that it works — the child spontaneously talks about their drawing, or asks to make another one.
  • ❌ To avoid — interpreting out loud (“ why did you draw in black? ”); we welcome, we do not analyze.
3

The Question Box

  • Objective — allow the child to ask the questions that worry them without having to say them face to face, often the most important ones.
  • Materials and duration — a small box with a slot, papers, a pencil placed next to it. We respond at a fixed time, for example, Saturday morning.
  • Procedure — the child slips their questions in whenever they want. At the agreed meeting time, we open them together and respond honestly. When we don’t know, we say: “I will ask the doctor.”
  • Easier (small) — the child draws their question, or dictates it for an adult to write down.
  • More difficult (big) — the teenager can note more abstract worries (future, money, reorganization).
  • Sign that it works — the box fills up, and the questions become more precise over time.
4

The Illness Word Notebook

  • Objective — provide the child with clear vocabulary (chemotherapy, infusion, fatigue, healing) to demystify words heard everywhere.
  • Materials and duration — the DYNSEO word notebook or a simple notebook, images, 10 minutes.
  • Procedure — one page per difficult word, with a very simple definition and a drawing. We fill it in as words come up in the family’s life, never all at once.
  • Easier — stick an image and say the word together.
  • More difficult — the child writes their own definition, then explains it to a brother or sister.
  • Sign that it works — a word that was scary becomes a word the child can explain without tensing up.

Maintain References and a Reassuring Routine

When illness disrupts family organization, what reassures a child the most is not that we promise them everything will be fine: it’s that breakfast remains breakfast, that the evening story takes place, that school continues. These four tools protect the framework, this foundation that does not change when everything else wobbles.

5

The Weekly Chart

  • Objective — make visible who takes care of the child each day, especially on treatment or hospitalization days, to eliminate uncertainty.
  • Materials and duration — a large wipeable board or a laminated sheet, pictograms or photos of the adult caregivers, 5 minutes on Sunday evening.
  • Procedure — we fill in the week together: who takes them to school, who picks them up, which days the parent is tired or absent. The child checks off or moves a magnet each morning.
  • Easier — only in the morning and evening, with photos of the people.
  • More difficult — the older child manages their own chart and anticipates their own activities.
  • Sign that it works — the child consults the chart by themselves instead of asking “who is picking me up?” with worry.
6

The Preserved Bedtime Ritual

  • Objective — protect the most sensitive moment of the day, when fears arise and sleep becomes fragile.
  • Materials and duration — nothing special, 15 minutes, at a stable time.
  • Procedure — keep the same sequence as before the illness: bath, story, cuddle, nightlight. If the sick parent cannot carry out the ritual, another adult takes over but keeps the same steps.
  • Easier — shorten without eliminating: a shorter story rather than no story.
  • More difficult — introduce a speaking time: “the best and the worst moment of your day.”
  • Sign that it works — falling asleep becomes easier again, and nighttime awakenings become less frequent.
7

The list "what doesn't change"

  • Objective — reassure by showing, in black and white, everything that remains stable despite the illness.
  • Material and duration — a sheet displayed in a visible place, 10 minutes once, to be reread later.
  • Procedure — we list together what continues: "we still love you just as much," "you still go to school," "on Wednesdays you still see grandma," "we still celebrate your birthday." We display it and complete it when a doubt arises.
  • Easier — only three things, illustrated.
  • Harder — the child adds what they need to be sure of themselves.
  • Sign it works — the child returns to the list when they are worried, or spontaneously mentions it.
8

The resource adults sheet

  • Objective — give the child the certainty that there is always a trusted adult available, even when their parents are absorbed by caregiving.
  • Material and duration — a sheet with the names, photos, and numbers of resource people (grandparents, neighbor, godmother, teacher), 15 minutes once.
  • Procedure — we build it together and place it at child height, near the phone. We calmly explain who to call in which case.
  • Easier — only two people, in photos.
  • Harder — the teenager records the contacts themselves and knows who to reach out to depending on the situation.
  • Sign it works — the child spontaneously knows who to turn to and no longer fears being "all alone."

Maintain the connection with the sick parent

The fatigue from treatments can significantly reduce the time available with the sick parent. The reflex is sometimes to postpone everything "until things get better." This is a mistake: for a child, five minutes of real presence are worth more than an entire day postponed. These three activities maintain the connection even on days of great fatigue.

9

The shared treasure box

  • Objective — create a common object that keeps the connection alive even at a distance, including during a hospitalization.
  • Material and duration — a nice box, small notes, drawings, photos, a few minutes when the desire comes.
  • Procedure — the child and the parent each place small things inside: a drawing, a pebble, a sweet note. When the parent is in the hospital, part of the box travels with them. We open it together upon their return.
  • Easier — only drawings exchanged.
  • Harder — keep a small "box journal" dated that we read together.
  • Sign it works — the child contributes to the box by themselves and looks forward to the moment of opening it.
10

The recorded message

  • Objective — maintain the voice and presence of the sick parent on days when they cannot be there physically.
  • Material and duration — a smartphone, 2 to 5 minutes.
  • Procedure — on good days, the parent records a story, a song, a simple "good night." The child can listen to it in the evening, or on treatment days. The voice reassures where the body cannot.
  • Easier — a single short good night message.
  • Harder — the child responds with their own message: an exchange is established.
  • Sign it works — the child asks for the message or proposes one in return.
  • ❌ To avoid — recording on a day of great fatigue a muted voice that would worry more than reassure; we choose a good moment.
11

The evening story in two voices

  • Objective — share a sweet and effortless moment, suitable even for a very tired parent, lying down.
  • Materials and duration — a book, a photo album, 10 minutes.
  • Procedure — the parent reads one page, the child the next, or the child reads while the parent listens, lying down, hand in hand. The lying position does not hinder anything: it is the presence that matters.
  • Easier — look at the pictures together, without reading.
  • More difficult — take turns inventing the continuation of the story.
  • Sign that it works — this moment becomes anticipated, an appointment that the child protects.

Finding the right words, at the right time

The DYNSEO training “When a parent has cancer: supporting their children in the face of illness” details, in 16 lessons, how to explain the illness according to age, identify signs of suffering, and preserve family balance. 100% online, at your own pace, unlimited access.

Discover the training — €20

Soothing, recharging, breathing

A child experiencing a parent's illness carries a tension they do not always know how to name. They need outlets: moments when we do not talk about the illness, when we play, when we breathe. These last three activities do not aim for any learning: they protect the mood and the child's right to remain a child.

12

The breathing balloon

  • Objective — offer the child a simple gesture to calm themselves when anxiety rises, without making it a medical exercise.
  • Materials and duration — the child's hands, or a stuffed animal placed on the belly, 2 to 3 minutes.
  • Procedure — we imagine a balloon in the belly: it gently inflates when we inhale, it deflates when we exhale. The child watches the stuffed animal rise and fall. We do it together, calmly.
  • Easier — blow out an imaginary candle three times.
  • More difficult — the child uses it alone when they feel tense and tells you about it afterward.
  • Sign that it works — the child uses it on their own in a difficult moment.
13

The calm corner

  • Objective — give the child a place of their own to retreat when the house is busy with care or visits.
  • Materials and duration — a corner, cushions, a blanket, a few books and soft objects; available at all times.
  • Procedure — we set up a refuge space together, a hut, a corner of the room. The child goes there whenever they want, without having to justify themselves. It is a place of retreat, never a punishment.
  • Easier — a simple dedicated cushion in a quiet corner.
  • More difficult — the child decides what to put in it and evolves their corner.
  • Sign that it works — the child retreats there on their own and comes out feeling calm.
14

The fun play session

  • Objective — decompress through play and find, for both the child and the parent, a light time without stakes.
  • Materials and duration — a board game, or a tablet with the COCO app for 5-10 year olds, 15 minutes.
  • Procedure — a genuine play moment, where we laugh, where we win and where we lose. The sick parent can participate from their chair or bed: a short game does not require energy.
  • Easier — a very simple card game, a single round.
  • More difficult — a cooperative game where we win together, which strengthens the family team spirit.
  • Sign that it works — laughter returns, and the game becomes a requested appointment.

A typical day and a typical week

The classic trap: wanting to do everything, every day, and turning the house into a permanent workshop. One proposal at a time is more than enough, as long as it really happens. Here is an example of organization to adapt to your reality, not a model to follow to the letter.

MomentWhat we includeDuration
Morning, before schoolA stable reference: check the weekly schedule, a hug5 min
After school, at snack timeA time available to talk if the child needs it10-15 min
End of the afternoonAn expression activity: drawing, jar of emotions10-15 min
Before dinnerCalm corner or breathing ball if tension rises5-10 min
EveningConnection with the sick parent: two-voice story, message10-15 min
BedtimePreserved bedtime ritual, nightlight15 min
DayPossible focus
MondayEmotions — jar of emotions, free drawing
TuesdayReferences — reread the weekly schedule and the list "what does not change"
WednesdayConnection — treasure box, recorded message
ThursdayCalmness — calm corner, breathing, fun play
FridaySpeech — open the question box, word notebook
SaturdayFun and social — outing, group game, see a friend
SundayNothing imposed. Rest and spontaneity are part of the program.
💡 Adapt to the energy of the day, not the other way around

Some days, there will be no room for anything, and that is normal. The schedule is a compass, not a contract. What matters is not checking all the boxes, but keeping at least one daily anchor point: often, the bedtime ritual is enough to keep the thread.

Arranging the child's environment

The environment speaks as much as words. A space designed for the child helps them find their bearings, calm down alone, and understand what surrounds them. Most of these arrangements cost almost nothing and can be set up in an afternoon.

SpaceWhat poses a problemWhat we change
The reference wallBlurred organization, uncertainty about the daysDisplay the weekly schedule, the adult relay sheet, and the list "what does not change" at child height
The child's roomDisturbed sleep, night fearsNightlight, reassuring object, stable order; avoid decorating upheavals during a crisis
The calm cornerNo place to retreat when the house is agitatedA dedicated refuge: cushions, blanket, books, soft noise-canceling headphones
The sick parent's spaceFatigue, need for rest, noiseA simple and non-anxiety-inducing signal (an image on the door) that says "I am resting"; explain that it is not a rejection
The screensPassive refuge, overexposure to anxiety-inducing imagesStable schedule framework, no screens at bedtime, vigilance on what the child sees or reads about the illness
The connection with the outsideIsolation, poorly informed schoolInform the teacher and school health services; maintain usual activities and friendships
💡 Informing the school changes a lot of things

Informing the teacher and, if possible, the school psychologist allows the child to be understood when they are distracted, tired, or on edge. School remains a precious place of normality: it is not betraying a secret to allow the adults surrounding the child to support them. A brief note is often enough.

The free supports and tools to print

Several DYNSEO tools, freely downloadable from the tool catalog, structure the entire routine described here. Three or four of them are enough: no need to print everything. They serve to keep track, to not forget anything during consultations, and to connect adults around the child.

  • Word notebook — the support for activity 4, to be personalized with the words of the illness that the child encounters.
  • Session tracking sheet — to note in one minute what was proposed, what calmed, what worried; useful for spotting what keeps coming back.
  • Communication notebook — to pass on your observations to the doctor, psychologist, or teacher without forgetting anything at the time of the appointment.
  • Progress tracking chart — a visual marker to follow, week after week, how the child's sleep, mood, or speech evolves.
  • Skills tracking chart — to visualize over time what is consolidating and what remains fragile.

These supports are not report cards. They primarily serve you: to make visible slow evolutions that daily memory erases, and to avoid arriving unprepared in front of the professional who asks you “how is it at home?”. To also explore the cognitive tests or the entire range of training, everything is gathered on the DYNSEO website.

The role of digital technology

A screen does not replace a conversation, a hug, or psychological follow-up. When used well, it brings two useful things during this period: a moment of shared play without stakes, and a support of attention and pleasure that adjusts itself to the level of the child or parent. When misused, it becomes a passive refuge: vigilance focuses on the framework.

ApplicationFor whomTypical use
COCOChild aged 5 to 1015 minutes of attention, logic, and memory games, in pairs with an adult
CLINTAdult, including the sick parent: support for morale and concentration15 minutes a day, 2 to 3 short games, including to combat the mental fog related to treatments
SCARLETTGrandparent involved in the support, simplified interfaceSame principle, with navigation designed for seniors
MY DICTIONARYSituations where speech is difficultVisual support for daily exchanges

The right dosage: short sessions, at fixed times, shared rather than solitary, and no screen in the last hour before bedtime, which weakens an already tested sleep. The application CLINT can also become a ritual for the sick parent: a moment of concentration for oneself, useful when treatment fatigue clouds attention.

The 5 most common mistakes

  1. Wanting to protect by silence. Saying nothing to “spare” the child has the opposite effect: they perceive the gravity, feel excluded, and fill the gaps with scenarios scarier than reality. The truth, told at their level, reassures.
  2. Assigning the child an adult role. “You have to be strong for mom,” “take care of your little brother”: these phrases reverse roles and deprive the child of their right to be supported. They can help, but never carry.
  3. Eliminating all light moments. Believing it would be indecent to laugh or play while a parent is sick. The child needs moments of carefree joy: they betray no one, they help to cope.
  4. Turning every exchange into an exercise. If everything becomes “activity,” the child shuts down. You are first and foremost a parent, an aunt, a grandparent: the relationship takes precedence over the method.
  5. Staying alone in the face of signs of suffering. Waiting for “it to pass” when sleep, mood, or school deteriorate durably. A doctor, school medicine, or a psychologist are there for that; asking for help early avoids many difficulties later.

To go further

Frequently asked questions

How often should these activities be proposed?

There is no universal good rhythm: the essential thing is regularity, not intensity. A small daily ritual, even five minutes, reassures more than a big moment once a week. In practice, one or two short times a day are sufficient: often a moment of expression after school and the evening ritual. Some days, fatigue or organization will leave no room for anything, and that is perfectly normal. It is better to protect a single anchor point held every day than to aim for an ambitious program abandoned after three days.

How much time should be dedicated to it?

Short sequences of ten to fifteen minutes are suitable for most children; younger ones get bored even faster. Always stop before fatigue or boredom, never when they are already there: an activity that ends well makes them want to start again. Duration matters less than the quality of presence: ten truly available minutes, without phone or parallel tasks, are worth much more than an hour of distraction. Also, let the child shorten if they have had enough: they set the pace.

How to motivate a child who refuses everything?

Never force: insistence closes doors. Three levers work better. First, propose without expecting an immediate response: settle in, draw yourself, and often the child will come. Next, replace the “serious” activity with a moment of play or pleasure that makes sense to them. Finally, respect the refusal without reproach: “not in the mood today? We’ll do it another day.” Refusal can sometimes be a way to express something. If it becomes a lasting withdrawal, talk to a professional.

What materials should be prepared?

Almost nothing: this is a principle of this toolbox. A box, a jar, markers, paper, a smartphone to record a voice, and possibly a tablet. The free DYNSEO resources (word notebook, tracking sheet, liaison notebook, tracking board) can be printed freely from the tools catalog. There is no need to buy specialized or expensive materials: effectiveness lies in regularity and presence, not in materials. The most important remains available without buying anything: attentive time and true words.

How to adapt according to the child's age?

Age changes the words and supports, not the principles. With a toddler, prioritize the concrete, the image, play, and very simple explanations; they mainly need reassurance that it is not their fault. With a school-aged child, you can name the illness, answer questions, and propose drawing or a question box. With a teenager, respect their need for privacy, inform them like a nearly adult without burdening them with responsibilities, and remain available without forcing. In case of doubt, a psychologist can provide useful guidance according to age.

ℹ️ Information and not medical advice

These activities and arrangements are general daily suggestions. They do not replace psychological follow-up, medical advice, or the support of the teams that assist your family. For any signs of distress in the child, consult the attending physician, school medicine, or a psychologist. In case of immediate danger, contact the emergency services in your country.

Support your children without facing the illness alone

Knowing what to implement when a parent has cancer is learned. The DYNSEO training “ When a parent has cancer : supporting their children in the face of illness ” includes 16 lessons to find the right words, identify signs of distress, and maintain family balance. 100 % online, unlimited access, certificate of completion. Certified organization Qualiopi (N° 11757351875).

Discover the training — 20 €

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