

Your hub for all of our patient information, from treatment information to real-life experiences, how you can get involved in our work, to clinical trials.
We are committed to ensuring our work and research is informed by the people it matters most to – people affected by prostate cancer. You can help us decide what projects to fund, meet our scientists, share your story, and more.
It’s common to be confused about PSA: what it is, what your PSA level means, whether you should have a PSA test and where you can get one. Read our article for answers to some of the most frequently asked questions about this test.
In March we will launch the first phase of our new patient education and information tool, provisionally called "The Infopool". Using this tool patients will be able to find out about potential future developments in prostate cancer diagnosis and treatment and participate in a short survey and/or patient panel. The aim of this research is to help make sure that future clinical trials are designed with you in mind.
There are a range of organisations providing support, including peer support groups, financial advice, nurse helplines, and health information.
If you would like to hear more, sign up to be kept up to date with our work.