Sex and side effects of cancer treatment

Side effects and your sexual well-being

Treatment for cancer affects each person differently. Before you start a treatment, your cancer team will explain what side effects you are most likely to have.

Side effects of cancer treatment can affect your sexual well-being. Not everyone will have the side effects we mention here. You may have side effects or questions that are not mentioned in this information. It is also important to remember your sexual well-being and relationships can be affected by more than just physical changes.

We have more information about cancer and relationships, and the emotional effects of cancer.

For each of the following side effects, we have included tips that might help and information about where to get support. We also have information about:

Your cancer team can answer any questions you have about your treatment. They will also tell you what to expect.

Booklets and resources

Coping with general side effects

Most people will have some general side effects. These usually get better, but they can affect your sexual well-being for a while.

Tiredness (fatigue)

During and after treatment, you might have less energy. You may need more rest or get tired easily. When you are tired, you may be less interested in sex or even in spending time with people.

If you have a partner, it might help to just spend time being close and intimate without having sex. Sometimes this can lead to sex. But it is also a way to build trust and confidence together.

If you want to have sex or masturbate, choose a comfortable and relaxed position. You may want to plan for a time of day when you have more energy. Do not put pressure on yourself to make it last a long time or to orgasm (come).

We have more information about coping with tiredness.

Feeling sick

Some cancer treatments can cause sickness and nausea. These treatments include chemotherapy and radiotherapy given near the tummy area (abdomen) or to the head. Other treatments can also cause sickness. Your cancer team will give you drugs to prevent and manage sickness. Tell your cancer team if you still feel sick. They can help.

Your treatment may only make you feel sick at certain times. For example, chemotherapy is most likely to make you feel sick in the hours or days after you have it. If you can work out when you usually feel sick, you can plan for when you are likely to feel more interested in sex.

We have more information on sickness and nausea.

Pain

Any type of pain can make you feel less interested in sex. You might not want to have sex because you feel uncomfortable. Or you might be worried that sex or masturbation will be painful.

It can help to try different things to find what works for you. You may want to do this by yourself or with a partner if you have one. This will help you discover which positions or types of touching feel comfortable for you.

If you have a partner, it can help to talk about how you are feeling. They may not want to have sex if they are worried about hurting you. Try to find a position that feels comfortable and relaxed for you both. Talking can help with any worries you may both have.

If you have pain in the pelvic area, you may want to try types of sexual contact that do not involve penetration. If you want to have vaginal or anal sex, using a lubricant may make things more comfortable. You can choose positions that allow you to control the depth and speed of penetration. Using a silicone penis ring during sex can also help control the depth.

You can also ask your cancer team or GP for advice about painkillers and ways to reduce the pain.

Coping with changes to how you look

Some treatments can cause changes to your appearance. This can be for a short time or permanent. The changes may include:

 

Some people find it takes time to adjust to changes like this. You may feel self-conscious or less confident because of your appearance. You may feel this way even if other people cannot see these changes.

If you find it hard to cope, give yourself time and be kind to yourself. You may find it gets easier. But if something about your appearance or body is stopping you from having relationships or sex, you may want more advice and support.

We have more information about coping with changes to how you look. If you have a partner, they may find this information helps them understand and support you.

 

Coping with lymphoedema

Lymphoedema is swelling caused by a build-up of fluid in the body’s tissues. Sometimes this is caused by cancer or treatments such as surgery or radiotherapy. Depending on the type of cancer, the swelling may affect:

  • an arm or leg
  • a breast
  • an area of the head or neck
  • an area of the pelvis, such as the vulva or penis and testicles.

This may affect your sex life or how you feel about your body. If you want to have sex, it may help to:

  • try positions that do not put weight on the affected area
  • have sex at times when the swelling is less – this might be in the morning, or after you have worn a compression garment for a few hours
  • use lots of lubricant to protect the skin if the vulva or penis and testicles are swollen.

We have more information about coping with lymphoedema. You can also get advice from your cancer team, GP or lymphoedema specialist.

Coping with mouth changes

Surgery or radiotherapy to the face, mouth or neck may change:

  • how you move your mouth and jaw
  • the feeling in these areas
  • your saliva (spit)
  • how you swallow.

Most difficulties will improve as you recover after treatment. Some may take longer or be permanent. They may affect how you feel about being intimate with a partner.

Give yourself time to adjust to any changes. Changes such as a dry mouth can often be improved, but you may need to try different things to find what helps.

If you are not comfortable with kissing or using your mouth during sex, tell your partner. There are other ways to give and receive pleasure. A sex therapist may be able to help if you need advice.

We have more information about coping with changes after treatment for head and neck cancer.

Coping with bowel problems

Some cancer treatments, such as pelvic radiotherapy or bowel surgery, can cause:

  • diarrhoea or loose stools (poo)
  • wind
  • needing to poo with little or no warning.

These effects may get better after treatment, but sometimes they are a long-term problem. They may make you feel embarrassed about being intimate with someone. They can also make you less interested in sex.

There are often ways to manage bowel problems. Your cancer team can give you medicines or advice about diet changes and exercises that may help. They may refer you to a specialist for treatment or more support.

These tips might help:

  • For a few hours before sex, avoid eating foods that make your bowel problems worse.
  • Go to the toilet just before you have sex.
  • Light scented candles if you are worried about smells.
  • Make sure you can get to the toilet quickly and easily.
  • Have tissues and towels nearby during sex.
  • Try an anal plug. This is a foam tampon you can wear in the back passage. It may be helpful for some people who cannot control when they need to poo. Anal plugs for bowel problems are available through the NHS. Ask your cancer team or GP for advice.

Coping with a stoma

Sometimes surgery to the bowel, or for bladder cancer, involves making an opening through the tummy wall. This is called a stoma. It allows either urine (pee) or stools (poo) to drain from the body into a bag that covers the stoma.

Having a stoma can affect your confidence and the way you feel about your body. Sex will not harm the stoma, but it can make some positions uncomfortable. Choose positions that do not put pressure on it. You should not use the stoma opening for penetrative sex.

These tips might help:

  • Make sure the stoma bag fits well and does not leak.
  • Empty the bag before sex.
  • Wear clothing that covers or supports the bag to keep it secure.
  • You may be able to plug the stoma or wash it out, so a bag is not needed for a short time. Ask your stoma nurse, cancer team or GP for advice.
  • Remember that your stoma is likely to be most active in the 2 hours after eating. Some foods can make the bag fill quickly. Avoid eating or drinking anything that usually causes you problems.

It can take time to get used to having a stoma. Your stoma nurses can give you advice and support. You can also find more information about sex and stomas from the Ileostomy and Internal Pouch Support Group.

Coping with breast or chest changes

The chest, breasts and nipples are sensitive areas of the body. They may be an important part of your sex life. They can also be important to how you feel about your body and sex.

Surgery for breast cancer can affect the nerves to parts of the chest, breast or nipple. Areas may feel numb or have less feeling than before. Sometimes this improves as you recover, but it may be permanent.

Surgery for breast cancer can also affect how the breast or chest looks. It may change the size or shape. Or it may leave scars.

If you have a whole breast removed, you may choose to have surgery to create a new breast shape. This is called breast reconstruction. The new breast may have less feeling or feel numb. We have more information about breast reconstruction.

Radiotherapy to the breasts or chest area can cause a skin reaction. The treated area may feel swollen, sore or tender until the skin heals. After treatment, the treated skin may permanently look or feel slightly different.

Give yourself time to recover after your treatment. You may want to experiment by yourself or with a partner to find what feels good now. A sex therapist may also be able to help you cope with changes to your body image or sensation issues.

Coping with loss of a limb

It can be hard to accept any major body changes, such as having an arm or leg removed. It can affect how you feel about your body and how your body works.

After this type of surgery, you will usually be fitted with an artificial arm or leg. This is called a prosthesis. Learning to use a prosthesis takes time. You may need to experiment to find what is comfortable for you during sex. If you have a partner, it can help to talk about how you both feel. A sex therapist may be able to help if you need advice.

It is up to you whether you wear your prosthesis during sex. It may help you hold a position, balance or move more easily. Or you may find sex is easier and more comfortable without it. Ask your physiotherapist or occupational therapist if you need advice about your prosthesis.

About our information

  • References

    Below is a sample of the sources used in our sex and cancer information. If you would like more information about the sources we use, please contact us at cancerinformationteam@macmillan.org.uk
    Katz A, Agrawal LS, Sirohi B. Sexuality after cancer as an unmet need: addressing disparities, achieving equality. American Society of Clinical Oncology Educational Book. 2022 Apr; (42):1-7. doi:10.1200/edbk_100032
    Sousa Rodrigues Guedes T, Barbosa Otoni Gonçalves Guedes M, de Castro Santana R, Costa da Silva JF, Almeida Gomes Dantas A, Ochandorena-Acha M, et al.. Sexual dysfunction in women with cancer: a systematic review of longitudinal studies. International Journal of Environmental Research and Public Health. 2022 Sep 21;19(19):11921. doi:10.3390/ijerph191911921
    Wittmann D, Mehta A, McCaughan E, Faraday M, Duby A, Matthew A, et al. Guidelines for sexual health care for prostate cancer patients: recommendations of an international panel. Movember. 2022. Available from: https://truenorth.movember.com/images/assets/SexualHealthGuidelines.pdf

  • This information has been written, revised and edited by Macmillan Cancer Support’s Cancer Information Development team. It has been approved by members of Macmillan’s Centre of Clinical Expertise.

    Our cancer information has been awarded the PIF TICK. Created by the Patient Information Forum, this quality mark shows we meet PIF’s 10 criteria for trustworthy health 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.

Date reviewed

Reviewed: 01 March 2024
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Next review: 01 March 2027
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.