Could you help a research team at the University of Liverpool who are planning to develop a mobile app which will support people living with Pelvic Radiation Disease?
The project team are inviting people living with PRD to share their views to help inform the development of the app.
For more details please see bit.ly/3FajlHk
Hello, this sounds like a good idea. I noticed that most of the group lives in England. I live in the USA. This would be a great tool
An excellent idea. I'm sure it would be of great help and reassurance to folk affected by PRD.
Newbie !
Late effects Clinic for Pelvic Radiation Disease now open in Bristol Cancer Institute Horfield Road Bristol
6 Months on and we’re making some progress 🌞🌞How can I get a PRD diagnosis when my GP is useless 
Hi Everyone, I'm new to this but so glad I found it. Thought I'd introduce myself....no point in holding back!
