- Cancer Information
- Schools and teachers
- Cancer in the school community
- Talking about cancer in schools
Talking about cancer in schools
Talking about cancer is never easy, and you may feel concerned about saying the wrong thing. It can also be challenging to balance a person’s right to privacy with the need for others to know about their diagnosis. Use your school’s existing well-being and communication guidelines and resources as you provide support.
Learn more about:
- Talking to someone with cancer
- Respecting privacy
- Appointing a school liaison person
- Understanding differences
- Communicating with people of all ages
- Different views of cancer
Listen to a podcast on Explaining Cancer to Kids
Talking to someone with cancer
People often say they don’t know how to talk to someone with cancer, and they feel lost for words.
Simply knowing that people are thinking of you helps to ease the isolation and anxiety.
The tips below can guide you, but the best advice is to just be yourself and try not to worry about whether you are saying the right thing. Saying something is often better than saying nothing because it acknowledges what is happening.
Listen and let them lead the conversation – If the conversation stops, it’s not necessary to fill in the gaps. Simply being there can be just as important as talking. They may also want to talk about other things rather than having cancer dominate every conversation.
Acknowledge their feelings – It’s okay for someone to feel sad or angry about their cancer diagnosis, so don’t try to change their feelings and don’t tell them to be positive. Let them cry or express themselves as they wish.
Avoid giving advice – Even if you have been in a similar situation, it is best not to tell the person what to do or that you know exactly how they feel. Try to use phrases like, “That sounds really difficult”, or, “You’re going through so much.”
Enjoy a laugh – People living with cancer want to talk about other things too. Not every conversation has to revolve around their diagnosis. Students, especially, see school as an opportunity for normality and routine.
Offer practical support – People overwhelmed by a cancer diagnosis often receive many open-ended offers of support (such as, “How can I help?”), but may prefer specific offers – for example, “I was thinking of organising some meals for you – would that be okay?” or “If Meg’s finding her bag a bit heavy, she can leave some of her books at school if she likes.”
Invite them places – If you used to eat lunch in the staff common room or sit together on playground duty, continue to ask the person along. If you think they are too ill, suggest another activity or join them where they are comfortable.
Students may find it difficult to talk to a peer with cancer. Find out how you can guide them in Talking to a classmate with cancer.
|Ways to provide practical support|
Go grocery shopping.Mind children or pets.Help with cleaning or laundry.Do some gardening.Make dinner.Drive to treatment.Meet for coffee.
Some people wish to keep their cancer diagnosis private. There can be a number of reasons for this:
- Students may see school as a place to be themselves and carry on with life as normal. Because fitting in with peers can be so important, they may want to minimise anything that makes them seem different.
- Parents or family members may want to avoid gossip or probing questions. Sometimes they need more time to talk to relatives or decide on treatment.
- A colleague with cancer may want to continue working and focus on their day-to-day activities, or they may wish to keep their diagnosis private until they know how it will affect their work schedule.
- Some teachers worry that their students are too young to understand cancer.
These are legitimate concerns, and people’s rights should be respected. Unless there are overriding health and safety issues, the person with cancer or their parent must give consent before anyone is told about the diagnosis.
In most cases, however, it will be easier for both the person with cancer and the school if at least key staff are aware of the diagnosis. An informed teacher can accommodate the person’s needs; anticipate questions from students, colleagues or families; and help to distribute information (if consent has been given).
The reality is that even very young students have heard of cancer. Open and honest conversation about cancer reduces the risk of confusion and anxiety and helps children of all ages understand. Being open about the diagnosis can also reduce the chance of gossip and misinformation circulating around the school community, particularly if treatment leads to changes in someone’s appearance (e.g. hair loss, amputation).
Any member of the school community who is provided with personal information about a student, student’s family or staff member, needs to treat the information sensitively and confidentially.
I didn’t want to share my diagnosis with everyone. Mum and I are both really private. I didn’t want people to treat me differently.
Appointing a school liaison person
If a student has cancer, one of the most helpful things you can do is to appoint a particular staff member as the key point of contact in the school. It may be the student’s main teacher but could also be another teacher or a member of the learning and support or wellbeing teams. To help avoid further stress, it is important that the student and their family feel comfortable with and have a good rapport with this person, and that the arrangement is reviewed regularly.
The school liaison person can keep up to date with the family’s changing needs and communicate with other staff on their behalf. They can also liaise with the hospital school and other education professionals. This reduces the chance of messages being misunderstood or the family having to repeat information.
It can be difficult to gauge the right level of contact and how much support is needed and welcomed by a family. The school community plays a central role in the lives of some families, but for others – often those with strong family networks – it is not as important. A family may not want help from the school.
If your school community includes diverse cultural groups, people will probably have different values and beliefs about health care. This will affect how they understand cancer and the level of stigma they attach to the disease. It can also influence how information is shared. In some cultures, cancer can have different meanings and some people may not want to talk about it openly. Some cultures believe that cancer is contagious, caused by bad luck or is always fatal. They may not want to use the word “cancer”. Others may believe the cancer has been sent to test them.
When you talk about cancer, be respectful of different ways of coping. For example, you can ask what kind of support a colleague, family or student would like, rather than assuming you know the best way to help. If the person is uncomfortable discussing cancer or has privacy concerns due to cultural reasons, they will be able to let you know.
As well as being culturally sensitive in your discussions, you can help by directing people to Cancer Council 13 11 20 for information about cancer and cancer services. If needed, they can call the Translating and Interpreting Service (TIS) on 13 14 50 and ask to speak to Cancer Council. Using a professional interpreting service maintains confidentiality. This can often be a better approach than using a family member or friend as an interpreter.
When a parent wishes to keep their own cancer diagnosis private, their children may be torn between respecting the parent’s wishes, and their own need for support. Organisations such as CanTeen may be able to help them.
There are many myths about cancer, which can make it difficult for people to talk openly about someone’s cancer diagnosis. Cancer is not:contagiouscaused by something someone has said, or a punishment for bad behaviourcaused by stressa death sentence.Visit Cancer Council’s iheard website for more information concerning common misconceptions about cancer.
Communicating with people of all ages
A person’s understanding of cancer depends on their age, maturity level and experience with the disease. When someone they know is diagnosed with cancer, they may have a range of reactions. These reactions depend on their relationship with the person, their personality and temperament, and the support they receive.
See Different views of cancer for an outline of how children, adolescents and adults without cancer may understand the disease, how they might react to someone’s cancer diagnosis, and how you can talk to them about it. Key treatment or testing milestones, including finishing treatment, can also prompt anxiety.
Be particularly alert for changes in behaviour. For example, a young child may regress to thumb-sucking, a sociable student may start to withdraw from peers, a top student’s grades may start to slip, or an even-tempered teacher may become moody. You can use these behavioural changes as a starting point for a supportive conversation. Provide opportunities for professional counselling if needed. Your school counsellor should be able to help.
Remember that each person is unique and these are broad guidelines. Although the experience of cancer is often challenging, many people are resilient and have positive reactions. For example, siblings of children with cancer often grow in compassion and empathy for the hardship of others.
Cancer words for kids provides definitions for some cancer-related words. It provides two versions of each definition: one that is suitable for younger children, and one that is more appropriate for older children, adolescents and adults.
Cancer Council’s information on Talking to Kids About Cancer may help you with strategies for discussing cancer with students from different age groups. Camp Quality offer a free educational program, which uses puppets to help preschool and primary school students understand and talk about cancer.
Different views of cancer
When someone in your school community is diagnosed with cancer, you are likely to encounter a range of reactions from students, families and colleagues. These general guidelines may help you pick up on signs of distress and provide age-appropriate support.
Early primary students (4–7 years)
In the early primary years, students have a basic understanding of sickness. When someone they know has cancer, they may worry that they will catch the disease or that they caused it (e.g. by being naughty or thinking bad thoughts about the person). At this age, most children are egocentric: they often think everything is related to them and may not yet empathise with others. They tend to notice (and comment on) physical changes. Young students may be just starting to realise that people, including parents or grandparents, can die.
- regression, e.g. stopping reading, starting to suck their thumb again
- comfort-seeking behaviours, e.g. using a security blanket or a special toy as a comfort object, thumb-sucking
- stuttering or baby talk
- withdrawing from conversations
- hiding behind a parent or significant adult when meeting other people
- fear of separation from others, especially at bedtime and going to school
- fear of the dark, monsters, animals, strangers and the unknown
- disturbed sleep, e.g. sleeplessness, wanting to sleep with a parent, sleepwalking or sleep talking, nightmares, bedwetting
- hyperactivity or apathy
- aggression, e.g. hitting or biting
- repeating questions about the same topic, even if it has been discussed several times
- commenting on physical changes and teasing if they don’t understand them
- listen to their feelings (expressed through speech or play) and be alert to their needs
- talk about cancer using picture books, dolls or stuffed animals
- read books together that explore anger, sadness and other feelings
- be honest (to their level of understanding)
- reassure them that they will be taken care of and will be safe
- if separation anxiety is a problem, ask them to look after something special for that person, so they know they will return
- provide brief and simple explanations, but use all of the cancer terminology they may encounter (see Cancer words for kids); repeat your explanations if necessary
- keep routines consistent where possible, and explain any changes to their schedule
- encourage them to have fun at school and enjoy their other activities; physical activity can help to release anxiety and tension
- assure them that they have not caused the cancer by their behaviour or thoughts, nor will they catch cancer
- continue usual discipline and limit-setting
Later primary students (7–12 years)
By the later primary years, most students are ready for more complex explanations of cancer and cells. Like younger children, they may feel responsible for causing the cancer of someone they know and may blame it on their own bad behaviour. Many are starting to comprehend the finality of death and its impact (especially if they have been exposed to death at a young age).
- irritability, anxiety, guilt, envy
- sadness, crying
- physical complaints, e.g. headaches, stomach-aches
- school refusal
- separation anxiety when going to school or away to camp
- hostile reactions, e.g. fighting or yelling
- poor concentration or daydreaming at school, possibly with a change in academic performance
- withdrawal from friends and family
- self-consciousness, feeling like the odd one out
- difficulty adapting to changes (such as a replacement teacher or new schedule)
- fear of performance, punishment or new situations
- sensitivity to shame and embarrassment
- trying to be extra good
- listen to their feelings (expressed through speech or play) and be alert to their needs
- use books to explain disease, cancer, treatment and potential outcomes
- assure them their behaviour or thoughts did not cause the cancer
- be honest
- reassure them about their care and schedule
- maintain clear rules and expectations
- assure them that the chances of someone else getting cancer are slim
- let them know how they can help a teacher, classmate, sibling or parent with cancer
- take time to listen and let them know you care about their feelings
- appoint a teacher, staff member or buddy to watch out for them
- if the prognosis is poor, ask for help from a social worker or psychologist to gently broach the topic of a parent, teacher or classmate dying
Secondary students (12–18 years)
By the secondary years, students are starting to think more like adults. As their ability for abstract thought develops, they recognise relationships between events, such as cause and effect. They now appreciate that people are fragile and can imagine what it might be like to have cancer.
- denying fear or worry to avoid discussion
- hiding feelings – parents, teachers and friends may not see true reactions
- anger, rebellion
- withdrawal, apathy, depression, anxiety
- worry about being different and not fitting in
- becoming nervous in social situations
- wanting to be independent and treated like adults – may become more responsible
- regression, e.g. watching children’s TV shows, being dependent on parents
- critical view of the support offered by adults and friends
- friendship issues
- poor judgement and risk-taking, e.g. smoking, binge drinking, unsafe sex, abuse of illicit or prescription drugs
- self-harm, e.g. cutting, restricting diet
- physical symptoms caused by stress, e.g. stomach-aches, headaches
- difficulty concentrating in class, change in academic performance
- poor school attendance
- a desire to help others and raise funds or awareness about cancer
- listen to them, don’t talk at them; encourage them to discuss their feelings, but realise they might not want to talk or may prefer to confide in friends
- express your feelings so they know what they’re feeling is normal (e.g. share that you are worried or miss the person), but do not burden them with the task of taking care of you
- provide privacy, as needed; highlight the importance of respecting privacy and using social media appropriately
- encourage them to maintain activities and friendships at school, if possible
- don’t expect them to take on too many extra responsibilities at school
- allow them to have time with friends
- allow flexibility and special consideration with schoolwork
- provide in-school opportunities for them to learn more about cancer and receive support; don’t expect them to be cancer experts
- treat them with respect as an emerging adult; let them know you are thinking about them, but be discreet and respectful
Parents and staff members (over 18 years)
Because adults and some older students can think in abstract terms, they usually empathise with the person affected by cancer. They understand complex relationships between events and are likely to recognise the impact of a cancer diagnosis and treatment on all aspects of life (such as school and personal relationships).
- depression, anxiety
- sadness about their own experiences with cancer
- physical symptoms such as headaches
- fear about their ability to cope
- feeling overwhelmed
- needing to talk with others about how they are feeling
- putting extra energy into work or distracting activities
- fluctuation in mood, especially around significant testing and treatment dates of the person with cancer
- keep in mind that different people will feel comfortable with different approaches
- take time to listen and let them know you care about their feelings
- if a student has cancer, principals can give staff simple and factual information and encourage them to seek further information as necessary; they can discuss strategies for supporting the child and their siblings, what information may be shared with students and their families, and how to talk to children about cancer
- if a staff member has cancer, they may choose to tell parents and students
- line managers can remind the person with cancer about any staff counselling services that they and their family can use, and discuss any requests for flexible working arrangements
Claire Tobin, Principal Medical Advisor, Department of Education and Training, VIC; Dr Antoinette Anazodo, Paediatric and Adolescent Oncologist, Sydney Children’s Hospital and Prince of Wales Hospital, Director of The Sydney Youth Cancer Service, and Conjoint Senior Researcher, University of New South Wales, NSW; Lisa Barrow, Clinical Nurse Educator, Children’s Cancer Centre, Royal Children’s Hospital, Melbourne, VIC; Margo Bulic, Psychosocial Support Worker, CanTeen, ACT; Amber Copeland, 13 11 20 Consultant, Cancer Council Queensland; Donna Drew, Clinical Nurse Consultant, Paediatric Oncology/Palliative Care, Kids Cancer Centre, Sydney Children’s Hospital, Randwick, NSW; Allesha Fecondo, Education Consultant, Victorian Paediatric Rehabilitation Service, and Education Liaison, Ronald McDonald Learning Program, Ronald McDonald House Charities Australia, VIC; John Friedsam, General Manager of Divisions, CanTeen Australia, NSW; Pina Hutcheson, President, Catholic Primary Principals’ Association of WA; Cara Irvine, Year 8 Coordinator, Alfred Deakin High School, ACT; Andrew Long, Assistant Director, Policy and Research, Independent Schools Council of Australia, ACT; Dr Alistair Lum, Post-doctoral Research Fellow – Behavioural Sciences Unit, Sydney Children’s Hospital, University of New South Wales, NSW; Kristine Luszczynski, Learning Program Manager, Quality and Standards, Ronald McDonald House Charities Australia, NSW; Anita Neville, National Manager, Ronald McDonald Learning Program, Ronald McDonald House Charities Australia, VIC; NSW Department of Education, NSW; Mandy Roney, Consumer; Shannon Rush, Primary School Program Manager, Camp Quality, SA; Luke Wade, Education and Career Support Consultant, Redkite, QLD.
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Dealing with the diagnosis
Common reactions to a cancer diagnosis and how to find hope
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Cancer in the School Community – Chapter 2
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