By letting your treatment team know what information you want and when, they can better meet your needs.
Information from your treatment team
To make choices about your treatment and prepare for it, you’re going to need information. Some people want to receive a lot of information about their cancer and treatment options, while others want only a little information at a time.
By letting your treatment team know what information you want and when, they can better meet your needs. You can let them know the level of detail you’d like and the format you’d prefer. For example, you may like to receive some information in person, or have leaflets to take away and read when you feel ready. The amount of information you want may change over time.
You can request information that meets your specific needs if you have a physical, visual or learning disability.
You can also request information in other languages and have an interpreter or advocate if you need. An advocate acts in your interests and helps to ensure your needs are understood and met.
Other sources of information
You may also get useful information from:
- Leaflets, booklets, and websites from the NHS, charities and other organisations
- Information events run by charities and other organisations
- Patient support groups (face-to-face groups, telephone support, online forums and social media groups)
- Other patients with secondary breast cancer
In this guide, we give sources of further online information, usually at the end of each page.
Breast Cancer Now’s health information is produced following best practice guidelines developed by the Patient Information Forum.
Find out more about how we develop our health information and the Patient Information Forum.