Overview
Many people have side effects from chemotherapy, which are caused when the chemotherapy drugs damage healthy, fast-growing cells.
Common side effects include fatigue, hair loss, nausea, and a higher risk of infection. Most side effects are temporary, and some can be managed or prevented. Talk to your treatment team about new or worsening symptoms.
What's on this page
Understanding side effects
Chemotherapy drugs can damage healthy, fast-growing cells, such as the new blood cells in bone marrow or cells in the mouth, stomach, skin, hair and reproductive organs. When healthy cells are damaged, it causes side effects.
Everyone reacts to chemotherapy treatment differently. You may have many side effects or a few. Whether you experience side effects and whether they are mild or severe can depend on the type and dose of drugs you’re given. Your reaction can also change over time.
If you have side effects, they may start during the first few weeks of treatment and occasionally become more intense with each treatment cycle. Before treatment begins, your doctor, pharmacist or nurse will discuss the side effects to watch out for or report, how to help prevent or manage them, and who to contact after hours if you need help.
It can be useful to keep a record of your chemotherapy treatment and any side effects you develop. This will help you remember when you had side effects, how long they lasted and what helped to make them better. You can use a notebook, diary or an app on a smartphone or tablet.
Tell your treatment team about all side effects. They will be able to suggest ways to manage the side effects or, if appropriate, they may change the treatment schedule or arrange a break.
List the doses and names of your chemotherapy drugs and any other medicine you’re taking, as well as the names of your specialists. Bring this list to all medical appointments, or if you become ill and need to visit a hospital emergency department.
How long side effects may last
How long side effects may last
Most side effects are short term, but some may be permanent. Side effects tend to gradually improve once treatment stops and the normal, healthy cells recover. Most side effects can be managed. Some side effects from chemotherapy may not show up for many months or years. These are called late effects. Before treatment starts, talk to your doctor about whether you’re at risk of developing late effects and ways to prevent them.
Long term and late effects of treatment
Long term and late effects of treatment
Permanent side effects of chemotherapy may include damage to your heart, lungs, kidneys, nerve endings or reproductive organs. If damage to your heart muscle or lungs is a possibility, your doctor will monitor how your heart and lungs are working and adjust your chemotherapy if early changes are seen. For more information, see Heart health and cancer.
Occasionally, years after having chemotherapy, some people develop a new, unrelated cancer. The risk of this is very low, but can increase with factors such as continuing to smoke or rare genetic conditions. If you notice symptoms, even many years after treatment, ask your GP whether they could be related to the cancer treatment you received. Ask whether your hospital has a late effects clinic to help you manage any side effects you may experience after treatment. Learn more about Living Well After Cancer.
Blood-related side effects
Blood cells are made in the bone marrow, which is the spongy part in the centre of the bones. The bone marrow makes 3 main types of blood cells, which have specific functions:
- red blood cells – carry oxygen around the body
- white blood cells – fight infection
- platelets – help blood to clot and prevent bruising.
New blood cells are constantly being made in the bone marrow. These rapidly dividing cells can be damaged by chemotherapy, and the number of blood cells (your blood count) will be reduced. Low numbers of blood cells may cause anaemia or bleeding problems, and increase the risk of infections.
You’ll have blood tests when you start treatment and before each chemotherapy cycle to check your blood count is okay before you continue. If your blood count has not recovered, your doctor may delay treatment.
Anaemia
Anaemia
If your red blood cell count drops below normal, this is called anaemia. A reduced amount of oxygen circulates through your body, which can make you feel tired, lethargic, dizzy or breathless. These tips for coping with fatigue may be helpful. To minimise dizziness, take your time when you get up from sitting or lying down.
Your treatment team will monitor your red blood cell levels. Let them know if you have any symptoms of anaemia during your course of chemotherapy. If the levels of red blood cells drop too low, you may need a blood transfusion to build them up again.
For more information, see Fatigue and cancer.
Bleeding problems
Bleeding problems
A low level of platelets (thrombocytopenia) can cause problems. You may bleed for longer than normal after minor cuts, have nosebleeds or bleeding gums, or bruise easily. Periods may be longer or heavier.
Your treatment team will monitor your platelet levels. If your level of platelets is too low, you may need a platelet transfusion. Ask your specialist to explain the risks and benefits of this procedure.
Contact your doctor or call Triple Zero (000) if you have persistent bleeding, such as a nosebleed, that doesn’t stop within 30 minutes.
How to manage a low platelet count
- Be careful when using knives, scissors or needles, as you may bleed easily from small cuts or nicks.
- Use an electric razor when shaving your face or body to reduce the chance of nicking yourself.
- Wear thick gloves when gardening to avoid injury. This will also prevent infection from soil, which contains bacteria.
- Avoid contact sports and high-impact activities, as these could cause bruising or bleeding if you get knocked or fall over.
- Blow your nose with care.
- Talk to your doctor before using aspirin or anti-inflammatory medicines such as ibuprofen as these medicines also increase your risk of heavy bleeding.
- Use a soft-bristled toothbrush to avoid irritating your gums.
- Wear comfortable, well-fitting shoes indoors and outdoors to avoid cuts on your feet.
- If you bleed, apply pressure to the area for about 10 minutes and bandage as needed.
- If you have problems with bleeding, talk to your doctor.
Infections
Infections
Chemotherapy can reduce your white blood cell level, making it harder for your body to fight bacterial infections. Bacterial infections that cause sickness may come from somewhere in your body (e.g. the bowel) and are not necessarily caught from other people. Viruses such as colds, flu and COVID-19 may be easier to catch and harder to shake off, and scratches or cuts may get infected more easily. Your doctor may recommend antibiotics as a precaution against infection. There are also other ways to reduce your infection risk.
There are many types of white blood cells. One type, called a neutrophil, protects you against infection by destroying harmful bacteria and yeasts that enter the body. Chemotherapy can reduce the levels of neutrophils. This is known as neutropenia.
To boost production of new white blood cells and protect you from infection, your doctor may give you injections of a growth factor drug called granulocyte-colony stimulating factor (G-CSF). Some people may experience bone pain or tenderness at the injection site. Let your doctor know if you have any of these side effects.
Taking care with infections during chemotherapy
Reduce your risk
To prevent the spread of infection:
- check your temperature regularly and any time you feel unwell
- avoid touching your eyes, nose and mouth with your hands
- check with your doctor about having flu and COVID-19 vaccines
- ask people close to you to consider having the flu and COVID-19 vaccines
- ask family and friends with a cold, flu or other contagious infection (e.g. COVID-19 or a cold sore) not to visit while they have symptoms
- try to avoid crowded places, such as shopping centres; if this is not possible, wear a face mask
- wash your hands with soap and water before preparing food and eating, and after using the toilet
- avoid drinking or cooking with untreated water (e.g. from rainwater tanks, bores and rivers); if you rely on rainwater for drinking or cooking, boil and cool the water before using it
- eat freshly cooked foods; avoid raw foods (fish, seafood, meat and eggs) and soft cheeses; wash fruits and vegetables well before eating; prepare and store food properly.
Having vaccinations
Some vaccinations are safe to have during chemotherapy treatment and others are not. It’s generally safe to have the flu vaccine and COVID-19 vaccines, but speak to your doctor before having these vaccinations.
During chemotherapy, and for about 6 months after, it’s often advised that you do not have vaccinations that contain a live vaccine, such as varicella (chickenpox), and MMR (measles, mumps, rubella) vaccines. Your doctor can give you more information.
When to seek help
Contact your doctor or go to the nearest hospital emergency department immediately if you experience one or more of the following symptoms:
- a temperature of 38°C or higher
- chills or shivering
- sweating, especially at night
- burning or stinging feeling when urinating (weeing)
- a severe cough or sore throat
- shortness of breath
- vomiting that lasts more than a few hours
- severe abdominal (belly) pain, constipation or diarrhoea
- unusual bleeding or bruising, such as heavy nosebleeds, blood in your urine (wee) or black faeces (poo)
- feeling faint or dizzy for a long time and having a rapid heartbeat
- any sudden worsening of your health.
Changes in your body
Nerve and muscle effects
Nerve and muscle effects
Some chemotherapy drugs can damage nerves between the central nervous system and the arms and legs. This is called chemotherapy-induced peripheral neuropathy (CIPN). It causes tingling (“pins and needles”), numbness or pain in hands and feet, and muscle weakness in legs. For many people, peripheral neuropathy is a short-term issue. But sometimes, it can last a longer time or be permanent. If you experience numbness and tingling, tell your doctor or nurse straightaway. Your treatment may need to be changed, or the problem carefully monitored.
Wearing special gloves and socks that compress or cool your hands and feet during chemotherapy may help prevent CIPN. These can only be used with certain chemotherapy drugs, and they don’t always stop it developing. Ask your treatment team if this option is available to you.
How to manage numb hands or feet
- Take care when moving around; you may be more likely to trip if your feet are numb or your legs are weak.
- Ask your treatment team about balance exercises, which may help manage some of the symptoms.
- Wear gloves and socks to keep warm. You can soak hands and feet in warm water to relieve symptoms.
- Wear shoes that fit well and have non-slippery soles.
- Clear walkways of hazards and remove loose rugs.
- Use your elbow to check the water temperature so you don’t burn yourself.
- Talk to an occupational therapist about aids that may help (e.g. posts to raise blankets off your feet in bed).
- If your symptoms are severe, talk to your doctor about medicines that may help or having a break from your treatment.
Fatigue
Fatigue
Feeling tired and lacking energy is one of the most common side effects of chemotherapy. It’s known as cancer-related fatigue.
You may also:
- develop muscle aches and pains
- have trouble thinking clearly or concentrating
- find it difficult to do daily tasks such as getting dressed, showering and cooking.
Fatigue can affect you suddenly and it doesn’t always get better with rest or sleep. If you find it hard to do everyday things, you might feel frustrated and isolated. Fatigue caused by chemotherapy may last for months or years after the treatment. However, many people find that their energy levels return to normal 6–12 months after treatment ends.
While fatigue is a common side effect of chemotherapy, it can also be a symptom of depression. If you have continued feelings of sadness, you may have depression, and treatment may help. For more information on depression, visit Beyond Blue and talk to your healthcare team.
For more, see Fatigue and cancer and listen to Cancer Council's podcast episodes Managing Cancer Fatigue and Sleep and Cancer.
I had no idea that I would still be feeling tired 5 months after finishing treatment. I didn’t know how to make it better and I was scared that’s how it would be: that I wouldn’t go back to normal, that I would never go back to having energy again.
How to manage fatigue
- Get extra rest the day of and day after chemotherapy to allow your body to recover.
- Plan activities for the time of day when you tend to feel most energetic.
- Try to be physically active with moderate exercise (e.g. walking, swimming) and some strength training (e.g. weights or resistance bands). See an accredited exercise physiologist or physiotherapist. They can develop a suitable program.
- Accept offers of help or ask family, friends and neighbours to help with shopping, driving, housework or gardening. Online tools such as GatherMyCrew can help organise this support.
- If you have children, ask trusted family and friends to look after them during your chemotherapy sessions and to be on call in case you become unwell afterwards.
- Eat a healthy, well-balanced diet and don’t skip meals.
- Try to limit how much you drink alcohol, smoke and vape.
- Try relaxation or meditation techniques to help reduce stress, improve your sleep and boost your energy levels. Listen to Cancer Council’s podcast Finding Calm During Cancer.
- Check with your doctor whether your fatigue is related to low levels of red blood cells (anaemia). Anaemia can be treated.
- Speak to your employer about how they can support you (e.g. you may be able to take a few weeks off, reduce your hours or work from home).
- Talk to your treatment team about trying acupuncture – some studies suggest this may help with reducing fatigue after chemotherapy.
- Contact your doctor or nurse if you have been too tired to get out of bed for more than 24 hours, or if you feel breathless or dizzy after a small amount of activity.
Hair loss
Hair loss
Whether you lose your hair will depend on the drugs prescribed. Some people lose all their hair (alopecia); others find it becomes thinner or they may lose only a little hair. Some people lose none at all. Although losing hair from the head is most common, eyebrows, eyelashes, hair from your underarms, legs, chest, beard and pubic area can also fall out.
When hair loss does occur, it usually starts during cycle 2 or 3 – or sometimes after the first cycle. It may be sudden or happen gradually. Before and while your hair is falling out, your scalp may feel hot, itchy, tender or tingly. Some people find that the skin on their head is extra sensitive, and they may develop pimples on their scalp.
It’s not unusual to feel sad or less confident. It may take time to adjust to how you look. Planning for hair loss may help you cope with it.
Hair growing back – After treatment ends, it can take 4–12 months to grow back a full head of hair. Hair usually grows about 1 cm every 4 weeks. When your hair first grows back, it may be a different colour, softer or curly (even if you have always had straight hair). In time, your hair usually returns to its original condition.
Scalp cooling – Some treatment centres provide cold caps, which may reduce hair loss from the head. Cold caps can only be used with certain drugs and some types of cancer, and they don’t always stop hair loss.
The cap is attached to a cooling unit and worn during chemotherapy. This reduces blood flow and the amount of chemotherapy drug that reaches the scalp. Some people find the cold cap uncomfortable, and the cold temperature may be painful. If you’re interested in trying a cold cap, ask your treatment centre if it’s an option for you.
How to manage hair loss
- Keep your hair and scalp very clean. Use a mild shampoo like baby shampoo. If you want to use moisturiser on your head, use sorbolene. Check with your nurse before using any other hair or skincare products on the scalp.
- Comb or brush your hair gently with a wide-tooth comb or a hairbrush with soft bristles.
- Explain to family and friends, especially children, that the chemotherapy may make your hair fall out.
- Consider cutting your hair before it falls out. Some people say this gives them a sense of control.
- Wear a wig, hat, turban or scarf, or go bare-headed – whatever feels best to you. If you prefer to leave your head bare, protect it from the sun and the cold.
- If you plan to wear a wig, you can match your own hair colour and style. Or consider a new colour or style for a bit of fun.
- Some treatment centres have wig loan services; call Cancer Connect on 13 11 20 for more information.
- Try using a pillowcase made from silk or bamboo as these smooth fabrics can decrease hair tangles.
- Avoid dyeing your hair during chemotherapy and for about 6 months afterwards to allow the hair to become stronger. Vegetable-based hair dyes may be gentler on the hair and scalp.
- If your eyelashes fall out, wear sunglasses outside to protect your eyes from dust and sunlight.
- If your eyebrows fall out, you may wish to wear reusable eyebrow wigs or transfers until they grow back.
- Contact Look Good Feel Better on 1800 650 960. This program helps people manage the appearance-related effects of cancer treatment.
Thinking and memory changes
Thinking and memory changes
It’s common for people to have difficulty concentrating, focusing and remembering things after they have had chemotherapy. This is called cancer-related cognitive impairment. Other terms used to describe this include “chemo brain”, “cancer fog” and “brain fog”.
Thinking and memory changes may be caused by treatment or medicines, the cancer itself, fatigue and sleep problems, or feeling stressed or depressed. These problems usually improve with time, although some people can experience issues for years. Tell your doctor about any thinking and memory changes you’re having.
How to manage changes
- Use a calendar or smartphone features, such as reminders, alarms or lists, to keep track of tasks, appointments, when to take medicines, birthdays, etc.
- Write down anything you need to remember (e.g. where you parked the car).
- Focus on one thing at a time (try not to multitask).
- Aim to get 7–8 hours of sleep each night. Deep sleep is important for memory and concentration.
- Do light exercise every day to help you stay alert and sleep better.
- Learn a new skill (e.g. take up a new hobby or do crosswords or puzzles).
- Talk to your family or workplace about changes to your concentration and memory. This can prevent misunderstandings and help them support you.
- Ask your doctor about online brain training programs, such as memory games or problem solving.
- For more information, see Changes in thinking and memory, and listen to Cancer Council's podcast episode Brain Fog and Cancer.
Mouth problems
Mouth problems
Some chemotherapy drugs can damage healthy cells in the mouth and cause mouth sores, ulcers (oral mucositis) or infections. Chemotherapy treatment may also reduce the amount of saliva (spit) in your mouth, make your saliva thick or sticky, or make your mouth dry. This is called xerostomia or dry mouth. If you notice any sores, ulcers or thickened saliva, or if you find it difficult to swallow, tell your doctor.
To learn more, see Mouth health and cancer treatment and Taste and smell changes.
How to look after your mouth
- Discuss any dental issues with your oncologist or haematologist before seeing the dentist. If you need to have any dental work, tell your dentist you’re having chemotherapy.
- Use a soft toothbrush to clean your teeth twice a day.
- Sip fluids, especially water, and eat moist foods such as casseroles or soups if you have a dry mouth.
- Soothe tender gums or mouth with plain yoghurt.
- Rinse your mouth often – when you wake up, after you eat or drink, and at bedtime. Ask your doctor, nurse or pharmacist what type of alcohol-free mouthwash to use. They may give you a recipe for a homemade mouthwash. Talk to your doctor or nurse about medicines to relieve pain.
- Try sucking on ice chips during chemotherapy to help prevent or reduce the severity of mouth ulcers.
- Blend foods to make them easier to eat. Try smoothies made of fruit and yoghurt.
- Avoid smoking, vaping and alcoholic drinks, as well as foods that are hot, spicy, acidic or coarse (e.g. nuts). These can make mouth sores worse.
Skin and nail changes
Skin and nail changes
Some chemotherapy drugs may cause your skin to peel, darken or become dry and itchy. During treatment, and for several months afterwards, your skin is likely to be more sensitive to the sun.
You may find your nails also change and become darker than usual or develop ridges or white lines across them. Your nails may also become brittle and dry or lift off the nail bed. These changes usually grow out. Avoid having your nails done at a nail salon, as this can increase the risk of infection during chemotherapy.
Ways to take care of your skin
- Use a soap-free wash when showering, and avoid showers that are too hot. Gently pat your skin dry with a towel.
- Use a good quality moisturising lotion or a cream containing the ingredient urea to help ease the dryness.
- Wear loose, non-restricting clothing made from soft cotton fabric instead of rough or synthetic fibres.
- Use mild detergent to wash your clothing if you have sensitive skin.
- Do not shave or wax until your skin has healed.
- Protect your skin from the sun when UV levels are 3 or above. Use an SPF 50 or SPF 50+ broad-spectrum, water-resistant sunscreen. Wear a broad-brimmed hat, protective clothing and sunglasses, and try to stay in the shade. This advice applies to everyone, but is very important for people having chemotherapy.
- Avoid chlorinated swimming pools as the water can make skin changes worse.
- If your skin becomes red or sore in the area where the intravenous device went in, let your doctor or nurse know immediately
Body odour
Body odour
Chemotherapy can affect your sense of smell and you may notice that your body odour is unpleasant. Talk to your cancer care team if you’re concerned about a change in body odour.
Changes in eating and digestion
Appetite changes, nausea or vomiting
Appetite changes, nausea or vomiting
It’s common for your appetite to change during chemotherapy. Sometimes you may not feel hungry, or you may prefer different types of food. The drugs may also temporarily change how food tastes.
Chemotherapy can make you feel sick (nauseated) or make you vomit. Not everyone feels sick during or after chemotherapy, but if nausea affects you, it usually starts a few days after your first treatment. Nausea may last a short time or for many hours and you may also vomit or retch (when you feel the need to vomit but can’t). Sometimes nausea lasts for days after treatment.
Often the best way to manage nausea is to prevent it from starting, so you’ll usually be given anti-nausea (antiemetic) medicine before, during and after your chemotherapy sessions. Anti-nausea medicine helps most people, but finding the right one can take time. If nausea or vomiting continues after using the prescribed medicine, let your nurse, doctor or pharmacist know early so that another medicine can be tried. Steroids may also be used to manage nausea and improve appetite.
Appetite changes, nausea or vomiting may lead to weight loss. Losing weight during chemotherapy can make some side effects worse or cause delays to your treatment. A dietitian can help you choose the best foods to minimise weight loss.
Being unable to keep liquids down because of vomiting can make you dehydrated. Signs of dehydration include a dry mouth and skin, dark urine (wee), dizziness and confusion. It’s not safe to be left alone if you’re vomiting a lot, as the confusion may make it difficult to realise you have become seriously dehydrated. If you think you may be dehydrated, contact your doctor.
How to manage appetite changes
Appetite loss
- Eat what you feel like, when you feel like it, but avoid going for long periods without eating.
- Try eating small snacks throughout the day rather than large meals.
- Avoid strong odours and cooking smells that may put you off eating. It might help to prepare meals ahead and freeze them for days you don’t feel like cooking.
- If the taste of certain foods has changed, don’t force yourself to eat them.
- If you don’t feel like eating solid foods, have drinks enriched with powdered milk, yoghurt or honey. Or try soup or scrambled eggs.
- Do not use nutritional supplements, vitamins or medicines without your doctor’s advice, as some products could affect how chemotherapy works.
- Ask a dietitian for advice on the best foods or nutritional supplements to have during treatment and recovery.
Nausea
- Have a light, bland meal before your treatment (e.g. soup with dry biscuits).
- Sip water or fluids throughout the day so you don’t get dehydrated. Sucking on ice cubes or iceblocks, or eating jelly, can increase fluid intake. If water tastes unpleasant, flavour it with ginger cordial, syrup or fruit juice, or drink milk-based beverages.
- If your stomach is upset, try drinking fizzy drinks such as soda water or dry ginger ale.
- If you wake up feeling sick, eat something small rather than skipping a meal.
- If you cannot keep fluids down, contact your doctor or hospital immediately. They may be able to treat the vomiting, or you may need to have fluids through an intravenous drip in hospital.
See Nutrition for people with cancer and listen to Cancer Council's podcast episode Appetite Loss and Nausea.
Constipation or diarrhoea
Constipation or diarrhoea
Some chemotherapy drugs, pain medicines and anti-nausea medicines can cause constipation or diarrhoea. If your bowel habits change during your treatment, talk to your doctor, pharmacist or nurse.
For some people, there will be ongoing bowel problems after cancer treatment has finished.
See Nutrition for people with cancer for more information on staying well nourished and meal ideas.
How to manage bowel changes
Constipation
- Eat more high-fibre foods, such as wholegrain bread and pasta, fruits and vegetables, bran, nuts and legumes (e.g. baked beans or lentils).
- If you’re having treatment for bowel cancer, ask your treatment team if there are any foods you should or shouldn’t eat to help avoid constipation.
- Drink plenty of fluids, both warm and cold. Prune, apple or pear juice can work well. Have a glass of water with each meal.
- Do some light exercise, such as walking.
- Ask your doctor about using a laxative, stool softener or fibre supplement.
- Avoid using medicines delivered through the rectum (e.g. enemas or suppositories) as they may cause infection.
- Let your treatment team know if you have constipation for more than 48 hours, so they can help.
Diarrhoea
- Choose bland foods such as clear broth, boiled rice or dry toast. Avoid spicy foods, wholegrain products, fatty or fried foods, rich sauces, and raw fruits or vegetables with skins or seeds.
- It may help to eat foods that are high in soluble fibre such as oats, white bread, white rice, bananas, nuts and pasta. This type of fibre helps bind the stool together.
- Limit alcohol, fruit juice, soft drinks, strong tea or coffee, and foods containing artificial sweeteners, as these stimulate the bowel.
- Drink plenty of water to help replace fluids lost through having diarrhoea.
- Talk to your treatment team. They may change the drugs or doses you’re on or suggest other solutions.
- If diarrhoea is severe or ongoing, let your treatment team know. It can cause dehydration and you may need to go to hospital.
Changes to your senses
Hearing loss and tinnitus
Hearing loss and tinnitus
Your doctor may recommend that you have a hearing test before you start treatment, and this may be repeated before each treatment cycle. You may be at risk of losing the ability to hear high-pitched sounds. Some types of chemotherapy drugs may also cause a continuous ringing noise in the ears known as tinnitus. These changes can happen alone or together, and can be temporary or permanent. Let your doctor know if you notice any change in your hearing.
Watery eyes
Watery eyes
This can be a symptom of a blocked tear duct, which can be caused by some chemotherapy drugs. Massaging the area regularly with a small towel soaked in warm water (compress) and using eye drops can help clear blockages. Let your cancer care team know if this issue is ongoing.
Sex, intimacy and fertility issues
Chemotherapy can affect your sex life and fertility in emotional and physical ways. These changes are common. Some changes may be only temporary, while others can be permanent.
Physical and emotional changes
Physical and emotional changes
You may notice a lack of interest in sex or a loss of desire (libido), or you may feel too tired or unwell to want to be intimate. You may also feel less confident about who you are and what you can do.
There may be physical reasons for not being able to have sex or not being interested in having sex (e.g. vaginal dryness or erection difficulties). Changes in how you look can also affect feelings of self-esteem and, in turn, your interest in sex.
If you have a partner, it may be helpful for them to understand the reasons why your libido has changed, and to know that people can usually have a fulfilling sex life after cancer, but it may take time. Some partners may feel concerned about having sex. They might be worried about injuring or hurting you, or being exposed to chemotherapy drugs during sex.
Even if some sexual activities are not always possible, there are many ways to express closeness. Talking openly to your partner about how you’re feeling can be difficult but it’s often very helpful. It’s important to take time to adapt to any changes. If you’re worried about changes to how you feel about yourself, your relationships or sexual functioning, you may find talking to a psychologist, sex therapist or counsellor helpful.
To learn more, see Sex, intimacy and cancer and listen to Cancer Council's podcast episode Sex and Cancer.
Using contraception
Using contraception
In most cases, your doctor will advise you to use some form of barrier contraception (condom, female condom or dental dam) during treatment and for a while after. This is to protect your partner from any chemotherapy drugs that may still be in your body fluids.
As chemotherapy drugs can harm an unborn baby, your doctor may talk to you about using contraception for some months after chemotherapy. Although chemotherapy often affects fertility, it doesn’t always. If you’re in a heterosexual relationship and sexually active, you’ll need to use a reliable form of contraception to avoid pregnancy while having treatment. Talk to your specialist immediately if you or your partner become pregnant.
Changes in fertility
Changes in fertility
Chemotherapy can affect your ability to have children (fertility). This may be temporary or permanent. If you may want to have a child in the future, talk to your doctor before starting chemotherapy about how the treatment might affect you and what options are available. Eggs (ova), embryos, ovarian tissue or sperm may be able to be stored for use at a later date. This needs to be done before chemotherapy starts. In some cases, hormone injections can reduce activity in the ovaries and protect eggs from being damaged by chemotherapy.
Effects of chemotherapy on ovaries
Some chemotherapy drugs can reduce the levels of hormones produced by the ovaries. This can cause your periods to become irregular or even stop for a while, but they often return to normal within a year of finishing treatment. If your periods don’t return, the ovaries may have stopped working, causing menopause. After menopause, you can’t get pregnant naturally.
Signs of menopause include hot flushes, night sweats, aching joints and dry or itchy skin. In the long term, menopause – particularly when it occurs under 40 – may cause bones to become weaker and break more easily. This is called osteoporosis. Talk to your treatment team or GP about ways to manage menopause symptoms.
Effects of chemotherapy on sperm
Some chemotherapy drugs can lower the number of sperm produced and reduce their ability to move. This can sometimes cause infertility, which may be temporary or permanent. The ability to have and keep an erection may also be affected (erectile dysfunction or impotence), but this is usually temporary. If erection issues are ongoing, talk to your doctor.
For more, see Fertility and cancer.
All my life I wanted to be a father. I didn’t want cancer to ruin my chances, so I stored my sperm before treatment started. I think of this as a bit of an insurance policy.
Complementary therapies and chemotherapy
Complementary therapies are sometimes used alongside standard medical treatments. They may offer physical, emotional and spiritual support, help manage side effects, and improve quality of life.
Some therapies have been proven to be safe and effective in scientific studies. For example, meditation, relaxation, massage and counselling can reduce anxiety, and acupuncture has been shown to reduce chemotherapy-induced nausea. Some studies suggest acupuncture may also reduce peripheral neuropathy and fatigue.
It’s important to talk to your doctors about any complementary therapies you’re using or thinking about trying, as some can interfere with your treatment or make any side effects worse.
Complementary therapies are different to alternative therapies, which are used instead of conventional medical treatments.
Alternative therapies are unlikely to be scientifically tested, may prevent successful treatment of the cancer and can be harmful. Cancer Council does not recommend the use of alternative therapies.
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