Pain

People with cancer may have pain for a number of reasons. Different healthcare professionals can help you manage your pain in hospital or at home.

About cancer pain

Many people with cancer will have pain at some point. But for most people, pain can be managed using:

  • different medicines
  • non-drug treatments and complementary therapies 
  • things you can do yourself.

Pain is very personal and everyone’s experience with pain is different. Two people with the same type of cancer may have different amounts of pain.

Pain does not always get worse if the cancer develops. But pain is more common in people with advanced cancer. Advanced cancer means the cancer has spread.

Booklets and resources

Types of pain

Your doctors or nurses may talk about pain in different ways. There are many types of pain. It can be described or grouped depending on:

  • how long it lasts
  • what makes it worse or better
  • the parts of the body that are affected.
 
  • Acute pain

    Acute pain often starts suddenly and feels ‘sharp’. It usually lasts days or weeks. Acute pain usually stops when the cause of the pain has been treated, or tissue in the area has healed.

    Acute pain can be caused by things such as:
    • an operation
    • a broken bone
    • an infection.

    If acute pain is not relieved, it may become chronic pain.

  • Chronic pain

    Chronic pain lasts for longer, usually for 3 months or more. Chronic pain is sometimes called persistent pain. It may be caused by the cancer. Or it can sometimes be due to an ongoing side effect or late effect of cancer treatments. Sometimes it can be caused by something not related to the cancer or the treatment.

    People who take long-acting painkillers to manage chronic pain will often also use short-acting painkillers when they need to.

    You may find the pain can get worse just before your take your next dose of long-acting painkiller. This can be because the effects of the long-acting painkillers are wearing off. Your doctors may need to increase the dose of long-acting painkillers if their effect is wearing off too soon.

  • Breakthrough pain

    If you are taking regular painkillers for chronic pain, you may still feel sudden pain. This is called breakthrough pain. It is common and usually feels like the chronic pain, only worse. Or it can feel different.

    Breakthrough pain may happen because:

    • the effect of the regular long-acting painkillers has worn off
    • the pain is worse at a certain time of day
    • you make a sudden movement, or you cough.

    Sometimes it is not clear what has caused the breakthrough pain.

    Breakthrough pain can last for a short time, or sometimes for longer periods. It may be treated with a short-acting painkiller. It is best to take the painkiller before the pain gets severe. Waiting longer before taking the painkiller can increase the time it takes for the painkiller to work.

  • Bone pain

    Cancer that has spread to the bones (secondary bone cancer) can cause pain. The pain can feel different to different people but may be a dull ache that does not go away. It is often worse when you move.

  • Soft tissue pain

    Soft tissue pain is when there is damage to, or pressure on, your organs or muscles. For example, when the liver is swollen it causes pain and discomfort in the tummy (abdomen).

  • Nerve pain (neuropathic pain)

    Nerve pain is caused by pressure on the nerves or by nerve damage. This may be due to the cancer or cancer treatments. You may have nerve pain at some times but not others. The area may feel numb or sensitive. The pain may be:

    • burning or tingling
    • stabbing or shooting
    • like pricking, tingling or numbness on the skin.

    Your doctor can prescribe drugs and other treatments to treat nerve pain.

  • Referred pain

    An injury or problem in one part of the body may sometimes cause someone to feel pain in a different part of the body. This is called referred pain. For example, someone with a swollen liver may feel pain in their right shoulder. This is because pain signals from the liver travel along the same nerves as signals from the skin of the right shoulder. The brain confuses the signals and thinks the pain is coming from a different place.

  • Phantom pain

    Some people may feel pain in a part of the body that has been removed. This is called phantom pain. For example, someone might feel pain after having a limb removed (amputated), or a breast removed (mastectomy). The cause of phantom pain is not always clear. It may happen because the brain remembers the part of the body that was removed and the links to the nerve signals.

    Phantom pain can cause different pain sensations that are very real to the people who experience it. It can improve with time and may eventually go away. It may be complicated to treat and is usually managed by expert doctors at a pain clinic.

How to talk about your pain

It is important to tell your doctor or nurse if you have pain and how it affects you.

Some people do not want to talk about the pain they have. They may worry that the pain means the cancer has got worse. They may feel they are complaining and that they should accept having pain. Or they may be anxious about becoming addicted to painkillers.

But controlling pain is an important part of your care. If your pain is well managed, it means you can do more of the things you want to do. This can help you stay more positive and active.

You can help manage your pain by:

  • being open with your healthcare team about the pain
  • describing the pain, where it is and how it affects your life
  • telling them if and when the pain gets worse or better
  • talking to them about any worries you have about the pain relief options.

Having a pain assessment

Your doctor or nurse will start by asking you different questions about the pain and how it is affecting you. This is called a pain assessment. A pain assessment will help your cancer team understand the type of pain you have.

They will ask you to describe the pain. If you are keeping a pain diary, they will also want to look at this. Keeping a record of the pain may show a pattern, even if you have notes for only a few days. This can be used to improve your pain control.

Your doctor will also usually examine you. If they need to check the cause of the pain, they may arrange some tests for you.

All this information helps your team, you and people caring for you to plan the best way to manage the pain.

Who can help when you have pain

Different health and social care professionals may be involved in managing your pain. It is important that you and the people caring for you know who to contact if you have problems.

  • GP

    When you are at home, your GP can talk to you about medicines or treatments to help control pain. They can prescribe painkillers and check with you to find out how well they are working. They can increase the dose of the painkiller or change you to a different drug if needed. Your GP can also contact your cancer doctor or nurse for further advice.

    Your GP can arrange for a district nurse to visit. They can also refer you to other healthcare professionals such as a specialist palliative care team or a pain team.

  • Cancer doctor or nurse

    If you meet with your cancer doctor (oncologist) or nurse regularly, it is important to tell them about any pain you have. They can explain what is causing the pain and how to manage it. Some people may need tests to find out the cause of the pain.

    Your cancer team may ask you to contact them if you have pain, or if it gets worse. It is important to follow their advice.

  • Community nurse

    A community nurse can visit you at home to help you manage your pain. They may sometimes be called a district nurse. They can check that your pain medicines and treatment are working. They can advise you about:

    • taking your medicines
    • different ways of managing the pain
    • getting equipment that helps make you more comfortable.
  • Physiotherapist

    A physiotherapist is someone who gives advice about exercise and mobility.

    They may be able to show you different ways of moving to help manage the pain. If pain is affecting how far you can walk, they can suggest ways to make getting around easier. For example, they can arrange walking aids or a wheelchair.

  • Occupational therapist (OT)

    An occupational therapist is someone who gives information, support and aids to help people with tasks. These may include washing, dressing, or making meals. An OT can help provide equipment to make you more comfortable. For example, they may suggest special cushions or mattresses. If you have difficulty moving around, they can arrange handrails and ramps for your home to help you move more easily. They can also suggest ways to improve your energy levels and be more active.

  • Pharmacist

    A pharmacist can check your prescription, give you advice about your medicines and tell you how they may affect you. Tell your pharmacist if you are buying any over-the-counter medicines. They can tell you whether it is safe to take them with your prescribed painkillers and other drugs.

  • Specialist palliative care team

    Specialist palliative care doctors and nurses are experts in managing symptoms such as pain. They also give emotional support. Specialist palliative care teams work in hospitals, in the community and in hospices. The team may also include:

    • a physiotherapist
    • an OT
    • a counsellor or psychologist
  • Counsellor or psychologist

    Some people find it helpful to meet with a counsellor or psychologist. This is a person who gives advice about managing feelings and behaviours. They can help you find ways to:

    • cope with the pain
    • deal with any worries or emotions that may be making the pain worse.
  • Pain team

    Many hospitals have specialist pain teams. The team includes doctors, nurses and usually a specialist doctor called an anaesthetist. Some teams also have a psychologist.

    Your GP, cancer doctor or specialist palliative care team can refer you to a pain team. This can be very useful if your pain is difficult to control or you need a nerve block or other specialist treatment. 

  • Hospice

    Sometimes it can help to spend some time in a hospice having your pain, symptoms and other problems treated. This may be for 1 to 2 weeks.

    Your community specialist palliative care team or GP can arrange this for you. If you are in hospital, the palliative care team can arrange for you to go into a hospice if you need more specialist symptom control before going home.

    In the hospice, the doctors and nurses can adjust your medicines to get better control of your pain. They can often do this more quickly than if you were at home. Once your pain is controlled, you can go home again. At home, your GP and community specialist palliative care team can continue to help you. Your GP will know about community palliative care and hospice services in your area.

Ways of taking cancer painkillers

Medicines used to treat pain are called analgesics. Analgesics are often called painkillers. This is the term we use in this content.

You may also be given other types of drugs to help relieve pain. These could include drugs to treat bone pain called bisphosphonates, or steroids to reduce swelling.

Your doctor or nurse will regularly assess your pain to make sure you are taking the right combination of medicines for you.

We have more information about ways of taking cancer painkillers.

Types of painkillers

Pain is often described as being mild, moderate or severe. Different types of painkillers can be effective for different levels of pain. Once your doctors and nurses have assessed your pain, they will prescribe the best painkillers to help control it. You may also be given other drugs to help relieve pain. These may include steroids and muscle relaxants.

We have more information about types of painkillers.

Managing pain with other treatments

Some people find non-drug treatments and complementary therapies helpful in managing pain. They can be used with painkillers, or sometimes on their own.

Some treatments, such as talking therapies, aim to relax and de-stress your mind and body. Some people use physical therapies to help relieve pain.

We have more information about managing pain with other treatments.

Get practical help

Coping with pain can be harder if you are anxious about things such as:

Getting help with these things may help you feel less stressed. This can help make pain easier to control.

Talk to your doctors and nurses about any concerns you have about treatment and side effects. You can also talk to one of our cancer nurses on the Macmillan Support Line by calling 0800 808 0000.

You may worry that pain will affect how you travel or attend appointments. If this is the case, you may find the Blue Badge scheme useful. This allows you to park in parking spaces closer to where you need to go.

A social worker can check what practical and social help you need. They can visit you at home to see if you need help with things like:

  • meals
  • personal care, such as washing and dressing
  • finances.

The local authority will then explain about services they can help with. Services vary in different areas. The local authority may suggest other community organisations that can help.

Voluntary and community organisations

Voluntary and community organisations may be able to offer support.

  • British Red Cross

    The British Red Cross has volunteers who can help you with things like shopping, posting letters or changing library books. They may be able to help you get to hospital appointments. They also lend equipment like wheelchairs and commodes (portable toilets). Services vary in different parts of the UK..

  • Living Made Easy

    Living Made Easy has information and advice for disabled people. They also have advisers and occupational therapists who can advise about mobility aids and equipment.

  • Scope

    Scope has practical information and emotional support and advice for disabled people.

  • Good Neighbour Schemes

    Some areas have schemes to help people with things like shopping, meeting other people or transport. These are often called good neighbour schemes and are usually run by social services or local community organisations. Contact your local council or look online to find out what is available in your area.

Feelings and pain

Being in pain can affect how you think and feel. Some people may feel frustrated, frightened or isolated.

When your pain is well controlled, it will improve the way you feel. It also means you can do the things you enjoy and see other people. Always talk to your doctor or nurse if the pain is not controlled.

Talking therapies such as cognitive behavioural therapy (CBT) may help you to manage pain. Meditation techniques such as mindfulness may also help.

Depression

If pain is not well controlled, you may feel depressed. You may have a low mood most of the time. You may also have difficulty sleeping or no appetite. The pain may feel worse and harder to cope with.

If you or people around you think you may be depressed, talk to your GP. They can help you to get the right treatment and support. They may suggest you see a counsellor or psychologist. Your GP may talk to you about taking anti-depressants to improve your mood or reduce anxiety.

Getting emotional support

If you feel okay emotionally, your physical pain may feel better. There are many people and organisations that can help you cope with difficult feelings. Non-medical treatments may also help. Ask your doctor or specialist palliative care nurse which ones would be best for you.

It can help to talk about your feelings. You could talk to your partner, a close friend or family member. If you do not tell them, they may not realise you have pain. They may not understand how the pain is making you feel, and why you are angry or upset.

You may prefer not to talk to anyone you know about your feelings. If this is the case, you can talk to your GP or specialist palliative care nurse. They can help by putting you in contact with a counsellor. You could also contact the British Association for Counselling and Psychotherapy. Or you can speak to Macmillan’s cancer support specialists on 0808 808 00 00.

  • Useful organisations

    Different organisations offer advice, support and information about pain:

  • Support groups

    It can often help to share how you are feeling with other people who understand what you are going through. Local support groups offer a chance to talk to other people who may also be managing pain. You can find a support group in your area.

  • Online support

    Many people find support on the internet. There are online support groups, social networking sites, forums, chat rooms and blogs for people affected by cancer. These include Macmillan's Online Community. You can use these to share your experiences, ask questions, get advice, or just read other people’s stories.

  • Spiritual support
    Spirituality can mean different things to different people. It may be religious, or it may be expressed through music, art, nature, or how you relate to your family or community.

    A person’s spirituality can be an important source of comfort and strength. Some people with cancer find their spiritual beliefs are challenged by their situation. They may experience ‘spiritual pain’ and feel abandoned or frightened. Sometimes they may withdraw from family and friends..

    You may find it helpful to talk through your thoughts and feelings with someone you trust. This may be a close friend or family member, a health and social care professional or a chaplain or religious leader. If you would prefer to talk to a non-religious counsellor or pastoral carer, your GP, specialist nurse or hospital doctor may be able to help you find one.

    All these people may be able to help you work out your thoughts and feelings.

About our information

This information has been written, revised and edited by Macmillan Cancer Support’s Cancer Information Development team. It has been reviewed by expert medical and health professionals and people living with cancer.

  • References
    Below is a sample of the sources used in our cancer pain information. If you would like more information about the sources we use, please contact us at informationproductionteam@macmillan.org.uk

    ESMO Management of Cancer Pain in Adult Patients. ESMO Clinical Practice Guidelines. 2018. Available from: www.esmo.org/guidelines/esmo-clinical-practice-guideline-cancer-pain [accessed 24/03/2025].

    NICE Palliative cancer care: Pain. 2025. Available from: cks.nice.org.uk/topics/palliative-cancer-care-pain/management/managing-pain-non-emergency/#management-of-breakthrough-pain [accessed 17/02/2025].

    Scottish Palliative Care Guidelines. Available from: https://rightdecisions.scot.nhs.uk/scottish-palliative-care-guidelines/ [accessed 17/02/2025].
Dr Ollie Minton, Macmillan National Clinical Adviser and Consultant in Palliative Medicine.

Professor Ollie Minton

Reviewer

Consultant in Palliative Medicine

University Hospitals Sussex

Date reviewed

Reviewed: 01 August 2025
|
Next review: 01 August 2028
Trusted Information Creator - Patient Information Forum
Trusted Information Creator - Patient Information Forum

Our cancer information meets the PIF TICK quality mark.

This means it is easy to use, up-to-date and based on the latest evidence. Learn more about how we produce our information.

The language we use


We want everyone affected by cancer to feel our information is written for them.


We want our information to be as clear as possible. To do this, we try to:

  • use plain English
  • explain medical words
  • use short sentences
  • use illustrations to explain text
  • structure the information clearly
  • make sure important points are clear.

We use gender-inclusive language and talk to our readers as ‘you’ so that everyone feels included. Where clinically necessary we use the terms ‘men’ and ‘women’ or ‘male’ and ‘female’. For example, we do so when talking about parts of the body or mentioning statistics or research about who is affected.


You can read more about how we produce our information here.