Page last updated: November 2025

The information on this webpage was adapted from Understanding Brain Tumours - A guide for people with cancer, their families and friends (2024 edition). This webpage was last updated in November2025.

Expert content reviewers:

This information was developed based on Australian and international clinical practice guidelines, and with the help of a range of health professionals and people affected by brain tumours:

  • Prof Lindy Jeffree, Director of Neurosurgery, Alfred Health, VIC
  • Caitriona Nienaber, 13 11 20 Consultant, Cancer Council WA
  • Prof Tamara Ownsworth, Clinical Neuropsychologist and Research Director, The Hopkins Centre, Griffith University, QLD
  • A/Prof Hao-Wen Sim, Medical Oncologist, The Kinghorn Cancer Centre and Chris O’Brien Lifehouse, NSW
  • Megan Trevethan, Clinical Specialist Occupational Therapy – Cancer and Lymphoedema Services, Princess Alexandra Hospital, QLD
  • Chris Twyford, Cancer Specialist Nurse, Canberra Health Services, Cancer and Ambulatory Support, ACT
  • Dr Adam Wells, Clinical Academic Consultant Neurosurgeon, The University of Adelaide, Royal Adelaide Hospital, SA

A brain or spinal cord tumour and its treatment can change how the mind and body work. You or your family members may notice changes in how you speak and your personality, memory and other thinking skills, movement, balance or coordination.

It's common to feel very tired. An occupational therapist can help you to manage the effects of this fatigue and give you strategies to cope.

Other types of changes you experience will depend on the part of the brain affected by the tumour and what treatment you have had. If you or your family feel like you are behaving differently, talk to your doctor, nurse and cancer care coordinator.

The changes may be difficult to handle, and they could affect how you feel about yourself and your relationships. Talking to a counsellor or someone who has had a similar experience may help.

Call Cancer Council 13 11 20 to see what support is available, or find more information at Building the Bridge to Life with Brain Cancer.

Rehabilitation

Rehabilitation is treatment designed to help people recover from or adjust to injury or disease. After treatment for a brain or spinal cord tumour, most people will have an assessment to identify what they need help with and ways to manage changes.

A range of health professionals offer various therapies to help restore your previous abilities or help you adjust to changes or long-term effects.

Types of rehabilitation

A range of therapies can support you in your recovery. These may be available at your cancer treatment centre, community therapy service or through a rehabilitation specialist at a rehabilitation hospital.

You may also be referred to individual allied health professionals (e.g. physiotherapist, occupational therapist) in private practice. Ask to see a therapist experienced in working with people after treatment for brain or spinal cord tumours.

  • Physiotherapy – your physical abilities may be affected. Physiotherapy can help you learn how to move more easily, develop muscle strength and improve balance. Moving and strengthening your muscles can reduce tiredness or weakness related to treatment. If you can’t move easily, you may be able to learn techniques, such as using a walking stick, to help you stay as independent as possible. A neurophysiotherapist specialises in treating physical changes caused by damage to the central nervous system. 
  • Cognitive rehabilitation – your memory, language skills, concentration, planning and problemsolving skills (executive function) may be affected. A neuropsychologist, speech pathologist or occupational therapist can help improve these cognitive skills. They may use memory strategies, speech therapy, technology such as calendars and reminder alerts, and word puzzles. 
  • Exercise  a physiotherapist or an exercise physiologist can give you advice on how to increase physical activity and exercise safely to improve circulation and mobility, reduce swelling, and increase both your heart and lung fitness. They will also help you find ways to return to activities you previously enjoyed. To find a physiotherapist in your area, visit the  Australian Physiotherapy Association and to find an accredited exercise physiologist, visit Exercise & Sports Science Australia.
  • Speech therapy – your ability to talk may be affected, which is often called aphasia. A speech pathologist could help to restore speech. Speech pathologists also work with people who have difficulty swallowing food and drink (called dysphagia). To find a certified practising speech pathologist, visit Speech Pathology Australia.
  • Sight – you may lose some or all of your sight as a result of a brain tumour, depending on what part of the brain is affected. Vision Australia can teach you tips and strategies to live independently.
  • Occupational therapy – if you are finding it harder to do everyday personal activities (e.g. showering, dressing, preparing a meal) or more complex activities (e.g. work and driving), an occupational therapist may be able to help. They can offer a range of strategies and aids to help you manage fatigue, physical and cognitive changes so you can improve or maintain your independence. To find an occupational therapist near you, visit Occupational Therapy Australia.

Your guide to best cancer care

A lot can happen in a hurry when you’re diagnosed with cancer. The  guide to best cancer care for brain tumours (high grade glioma) can help you make sense of what should happen.

It will help you with what questions to ask your health professionals to make sure you receive the best care at every step.

Read the guide

Managing seizures

A brain tumour or its treatment can sometimes cause seizures (fits or convulsions), which are disruptions to the normal patterns of electrical impulses in the brain.

Types of seizures

Seizures can be divided into two main groups.

Generalised seizures

These occur when the whole brain is affected, and typically involve the whole body. The most common type is called a tonic-clonic seizure (previous known as a grand mal seizure).

A seizure often starts with a loss of consciousness. The person’s muscles may stiffen, their limbs may jerk rhythmically, and their breathing may be shallow for up to two minutes. They may bite their tongue, and lose bladder and bowel control.

Focal seizures

Also called partial seizures, these occur when one area (lobe) of the brain is affected. Focal seizures affect one part of the body, such as an arm or leg.

Symptoms of focal seizures depend on the area of the brain involved and may include:

  • twitching, jerking, tingling or numbness
  • not being able to speak
  • changes in vision or hearing
  • strange tastes or smells
  • a feeling of deja vu

Focal seizures may also cause a brief loss of consciousness, changes in mood, and memory loss just before, during and after the seizure.

Ways to prevent seizures

Seizures can often be prevented with anticonvulsant medicines (also called anti-epileptic or anti-seizure medicines).

Feeling overstimulated or very tired can also increase your risk of having a seizure. Try to get 6–8 hours sleep each night. Drinking less alcohol may also help.

How to help someone having a seizure

  • Remain calm and stay with the person while they are having a seizure. Refer to their Seizure Management Plan, if they have one.
  • Do not hold them down or put anything in their mouth.
  • Protect the person from injury (e.g. move hazards, lower them to the floor if possible, loosen their clothing, cushion their head and shoulders).
  • Call Triple Zero (000) for an ambulance if it is the first seizure the person has had, if the person is injured, if there was food or fluid in the person’s mouth, if the seizure lasts longer than five minutes or if you are unsure what to do.
  • Time how long the seizure lasts so you can tell the paramedics.
  • After the jerking stops, roll the person onto their side to keep their airway clear. This is particularly important if the person has vomited, is unconscious or has food or fluid in their mouth.
  • Watch the person until they have recovered, or the ambulance arrives.
  • If the seizure occurs while the person is in a wheelchair or car, support their head and leave them safely strapped in their seat until the seizure is over. Afterwards, remove the person from their seat, if possible. Roll them onto their side if there is food, fluid or vomit in their mouth.
  • Explain to the person what has occurred. In many cases, people are confused after a seizure.
  • Allow the person to rest afterwards as most seizures are exhausting.
  • For detailed information and an online tool for creating a Seizure Management Plan, contact Epilepsy Action Australia

 

Anticonvulsant medicines

Different types of anticonvulsant drugs are used to prevent seizures. You may need to have blood tests while you are taking anticonvulsants. This is to check whether the dose is working and how your liver is coping.

Side effects of anticonvulsant drugs vary, but they may include tiredness, gum problems, shakes (tremors), nausea, vomiting, weight changes, depression, irritability and aggression.

If you are allergic to the medicine, you may get a rash. Tell your treatment team if you have any skin changes or other side effects. Your doctor can adjust the dose or try another anticonvulsant.

Do not stop taking the medicine or change the dose without your doctor’s advice. If you take anticonvulsants, you may need to avoid some foods.

Check with your doctor before taking any herbal medicines, as these can change the way some anticonvulsants work.  Ask your doctor or pharmacist about potential interactions and foods to avoid.

Driving

Tumours, seizures, and certain treatments and medicines (such as anticonvulsants and some pain medicines) can affect the skills needed to drive safely. These skills include:

  • good vision and perception
  • the ability to concentrate and plan
  • processing speed and reaction time
  • ability to remember directions
  • good hand–eye coordination.
  • planning and problem-solving.

When you are diagnosed with any type of brain tumour, it is very important to ask your doctor how your condition or treatment will affect your ability to drive. Your doctor will usually advise you not to drive for a while.

You probably need to wait for some time before you drive again after surgery and possibly after radiation therapy. There are also some set exclusion periods your doctor will follow after certain treatments or events such as seizures.

If you have had seizures, legally you will need to be seizure-free for a period of time before you are allowed to drive. If you stop taking your anticonvulsant medicines, you will also need to be seizure-free for a period of time until you are allowed to drive.

Before you start driving again, always check with your doctor. Laws in Australia require drivers to let their driver licensing authority know about any permanent or long-term illness or injury that is likely to affect their ability to drive.

Your doctor can tell you if you should report your condition or if there are any temporary restrictions. The licensing authority may ask for information from your doctor to decide if you are medically fit to drive. 

Returning to driving

  • Have a driving assessment to check your ability to return to driving. This may include doing an off-road assessment or having an electroencephalogram (EEG) to assess seizure risk.
  • See an occupational therapist driving assessor, a neurologist or rehabilitation specialist to work out the type of problems you may experience while driving (e.g. a slow reaction time). The focus of the assessment is not to suspend or cancel your licence: it is to work out if it is possible for you to safely return to driving.
  • An occupational therapist may be able to teach you driving techniques to help with weaknesses or show you how to make changes to your car (such as extra mirrors). You may also be able to drive with restrictions, such as only in daylight, only in automatic cars or only short distances from home.
  • Some people feel upset or frustrated if they have licence restrictions or can no longer drive. You may feel that you have lost your independence or worry about the impact on your family. It may help to talk to a counsellor or someone who has been through a similar experience. Depending on your situation and your health, it may be possible to return to driving later on.
  • Follow any licence restrictions. If your doctor says you are not safe to drive, you must not drive unless they change that medical decision. If you ignore the restrictions, your licence may be suspended or cancelled. You may be fined if you drive while your licence has been suspended or cancelled. If you have an accident while driving, you could be charged with a criminal offence and your insurance policy will no longer be valid.
  • Talk to your doctor or visit Austroads.

Financial support for people with disabilities

The National Disability Insurance Scheme (NDIS) provides Australians aged under 65 who have a permanent and significant disability with funding for support and services.

The NDIS may be able to help a person whose everyday activities have been impacted by a brain tumour. For more information, talk with your GP or rehabilitation team.

If your GP refers you to a rehabilitation specialist as part of a Chronic Disease GP Management Plan or Team Care Arrangement, you may be eligible for a Medicare rebate for up to five visits each year.

Learn more

Working

It can be hard to predict how well you will recover from treatment for a brain tumour, and if or when you will be able to return to work. This may also depend on the type of work you do.

Some people find it hard to concentrate or make decisions after treatment for a brain tumour. At least at first, it may not be safe to operate heavy machinery or take on a lot of responsibility.

Your doctors and an occupational therapist can tell you whether it's okay to return to work. Talk to your employer about adjusting your duties or hours until you have recovered.

In some cases, it won’t be possible to return to your former role. It may help to talk to a social worker, occupational therapist or psychologist, call Cancer Council 13 11 20 or join a brain tumour support group to try and come to terms with these changes.

“I had a craniotomy for a benign brain tumour, but they couldn’t take all the tumour out. Later I had radiation therapy. Part of the tumour is still there, but it is stable, so I have been able to return to work and I can now drive again.” Debbie

Life after treatment

Some people continue to have regular treatment, but for those who finish their treatment, the cancer experience doesn’t usually end there. Life after cancer treatment can present its own challenges.

You may have mixed feelings when treatment ends, and worry about the cancer coming back. Some people say that they feel pressure to return to “normal life”.

It is important to allow yourself time to adjust to the physical and emotional changes, and establish a new daily routine at your own pace. Your family and friends may also need time to adjust.

Follow-up appointments

After treatment ends, you will have regular appointments to monitor your health, manage any long-term side effects and check that the tumour hasn’t come back or spread.

During these check-ups, you will usually have a physical examination and you may have blood tests or MRI scans. How often you see your doctor will depend on the type of tumour and treatments you had.

Between follow-up appointments, let your doctor know immediately of any new or changing symptoms or health problems. When a follow-up appointment is approaching, you may feel anxious. Talk to your treatment team for help managing this.

Get support

 Recurrence

For some people, a brain or spinal cord tumour can come back or keep growing despite treatment. If the tumour returns, this is called a recurrence.

Your treatment options will depend on your situation and the treatments you’ve already had, but may include surgery, radiation therapy combined with drug therapies including chemotherapy, or another systemic therapy.

Targeted therapy drugs attack specific features of cancer cells. Bevacizumab is a targeted therapy drug that can be used to treat advanced brain cancer. Bevacizumab is most helpful when the tumour is causing swelling in the brain. Your doctor will talk to you about the benefits and possible risks.

Other targeted therapy drugs and immunotherapy may be available on clinical trials. Talk with your doctor about the latest developments and whether you are a suitable candidate.

Understanding Brain Tumours

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