Life after transplant for acute myeloid leukaemia (AML)

It takes a long time to get over intensive treatment such as a stem cell or bone marrow transplant. At first you may have mixed feelings about going home. Your nurse will give you numbers to call if you have any questions or worries and you’ll have regular follow up appointments.

Your central line Open a glossary item usually stays in for a little while after treatment finishes. Your nurse can use it for blood tests at your follow up appointments. And some people still need platelet transfusions Open a glossary item or blood transfusions Open a glossary item.

It’s likely that you will get at least one infection after your transplant. This means you’ll need to stay in hospital again. This can be quite upsetting for you if you haven’t been home for long. Let the team know if you are struggling to cope, as there are ways that people can help you.   

You’ll start to feel stronger and more active again as time passes. But it takes a long time to get back to normal. It might be as long as a year before you really feel you are on the road to recovery.

Eating and drinking

During your transplant your treatment team may have advised you to make changes to your diet to reduce the chance of picking up an infection from your food. You might need to follow the same advice for the first few months after a transplant. The advice can vary slightly between hospitals.  

The general advice is to:

  • eat only freshly cooked food
  • avoid undercooked eggs
  • avoid soft cheese and blue cheese
  • avoid creamy cakes and puddings
  • avoid shellfish
  • wash salads and fruit very thoroughly
  • avoid takeaways and fast food restaurants (or make sure they make you freshly cooked food)

Don't drink more than the recommended amount of alcohol. Too much alcohol can slow the recovery of your bone marrow. Ask your doctor if alcohol will interfere with any medicines you are taking.

In general, the NHS recommends that:

  • you drink no more than 14 units of alcohol a week
  • if you drink this amount, to spread this evenly over at least 3 days
  • to have some alcohol free days in the week to help cut down on the amount you drink

Your social life

Reduce your risk of infection by avoiding:

  • crowded public places, such as cinemas or public transport at peak times for example
  • anyone with infections or anyone who you know has come into contact with infections, such as chicken pox or measles

Once your white cell count has recovered enough you will be able to go just about anywhere. This takes roughly 3 to 6 months but check with your doctor or nurse to be sure.

College, university or work

You won’t be able to go back to normal daily activity until your white blood cell levels are almost normal. It's a good idea to start part time until you have got some of your strength back. Talk to your employer, teacher or tutor about this. 

You might also want to think about whether you would like them to talk to your colleagues or peers about your illness and treatment. Or you might prefer to talk to them yourself.

Sport and physical activity

Physical activity is a great way to help you feel better, both physically and emotionally. It can help to reduce tiredness (fatigue) after treatment. How much you can do will depend on how fit you are and how you feel. You will probably have days when you don’t have so much energy. Listen to your body and build up slowly.

Gentle walking is suitable for most people to start with. If you don't have a central line, you can do most contact sports and swimming once your blood counts are back to normal and you feel up to it.

Ask your doctor or specialist nurse when you can do more physical and strenuous activities.

Holidays and travel

Before you go

Speak to your doctor before booking a holiday. Most people can go away but to begin with it’s best to stay in the UK. You can’t travel by plane if your platelets are too low.

Whenever you go away from the hospital that treated you it is helpful to carry a doctor's letter with you. This gives a summary of the treatment you have had and any medicines you are taking.  It includes a contact phone number for emergencies.

After the first year, you can go where you like. But you need to avoid having some vaccinations. And following an allogenic transplant Open a glossary item, you should not have live vaccinations.

Travel insurance

It's important to arrange travel insurance if you want to travel abroad. It’s there to help you get compensation for anything that might go wrong with your travel. Its also there if you need to claim back compensation for any medical treatment you have while you are in another country.

Getting travel insurance when you have or have had cancer can be difficult and expensive. This is because insurance companies only make money from people who don't claim. Because you’ve been ill, they think you’re more likely to claim. For example, you might need to cancel your trip or have medical treatment abroad. This makes you a bigger risk to the company. So they might:

  • refuse to give you travel insurance

  • give you travel insurance, but it’s likely to be very expensive

If a company agrees to insure you, they will almost certainly ask for a letter from your consultant about your fitness to travel. As the time since your treatment increases, you will find getting travel insurance easier.

You may also be able to get a free Global Health Insurance Card (GHIC) if you are travelling in Europe. You can apply for this online on the NHS website.

Your sex life

A transplant doesn't physically stop you from having your normal sex life. But you might find that your sex drive and self esteem are low for a while. This may be due to:

  • the treatment
  • lack of strength and energy
  • worry about the future
  • feeling upset about losing your fertility
  • lack of confidence after the changes in your appearance that a transplant causes at first (for example, hair loss)
  • getting used to changes in sex hormone levels

Some of these effects take time to get used to. Some will get better on their own. For example, your hair will grow back and you will put on weight.

It is important to give yourself time to recover. It can also help to keep talking to your partner, if you have one, about how you are both feeling.

You can always talk to your nurse or doctor if you are having any problems with your sex life. They can help you get the support and advice you may need.

Your feelings

You’ve been through a lot and it can take time to get back to a new sense of normal. It can be difficult to get back to work and family life. You may feel frustrated that you don’t feel as well as you hoped as quickly as you would like. There may be set backs along the way, and you may be in and out of hospital for a while.

After going through such intensive treatment some people may feel a new enthusiasm for life and appreciate the simple things. Other people may find it difficult to cope with and make sense of what they have been through. Some people may have anxiety or depression.

It’s important to talk things through with people around you or your doctors or nurses. They can help you get more help if you need it. Many people find it helpful to have counselling.

  • The EBMT Handbook. Hematopoietic Stem Cell Transplantation and Cellular Therapies
    E Carreras and others
    Springer Open, 2019

  • The European Blood and Marrow Transplantation Textbook for Nurses
    EBMT, M Kenyon and A Babic
    Springer Open, 2018

  • UK Chief Medical Officers’ Low Risk Drinking Guidelines
    Department of Health, August 2016

  • Hoffbrand's Essential Haematology (8th Edition)
    A V Hoffbrand and P Steensma
    Wiley Blackwell, 2019

  • Late effects of blood and marrow transplantation
    Y Inamoto and S J Lee
    Haematologica, 2017. Volume 102, Issue 4, Pages 614 to 625

  • The information on this page is based on literature searches and specialist checking. We used many references and there are too many to list here. Please contact patientinformation@cancer.org.uk with details of the particular issue you are interested in if you need additional references for this information.

Last reviewed: 
13 Nov 2023
Next review due: 
13 Nov 2026

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