[31st January 2025]

Karen shares her experience with the late effects of treatment for anal cancer. Despite the challenges, her strength and resilience shine through. She highlights the importance of informed consent and raising awareness about potential long-term effects of treatment.

Read Karen’s story

Karen lives in the USA, where she received her treatment. It is important to acknowledge that treatment options and care can vary significantly, whether in the UK or overseas. We strongly encourage you to discuss any concerns with your healthcare provider. The PRDA is a UK charity and the PRD Best Practice Pathway is designed based on UK signposting and NHS care.

“…[I] needed to know where a bathroom was at all times. Many accidents occurred over the years. This has been the most difficult side effect.” 

  • Share your story – We are committed to sharing the stories and voices of those living with PRD. If you’d like to share your experience of PRD, we’d love to hear from you. Share your experience of PRD
  • Support – If you would like to connect with other people with PRD, you are welcome to join our friendly Online Community – a safe and supportive space for people living with Pelvic Radiation Disease (PRD) to share their experiences, ask questions, and learn from others.

To find out more about our support services, please visit our Support page.