You’re welcome to share positive and/or negative stories and it can be as short or a long as you wish, although we may not be able to publish all story submissions in full.
Not sure where to start? Here are some questions that can help:
- How did you find out about Pelvic Radiation Disease?
- What information did you have about PRD/Late Effects prior to your treatment?
- How long after your RT did you first notice PRD symptoms?
- What symptoms do you experience?
- How does PRD impact your daily life? (diet, sleep, relationships, travel, work, hobbies, shopping, exercise, finances, etc)
- How does it make you feel?
- Have you had to make changes to your life to manage your PRD?
- What advice, information, support or treatment have you found/been offered?
- Has this advice, information, support or treatment been helpful?
- Have you been referred to any late effects or specialist services for PRD?
- What health services would you most like to be available to people with PRD, or at risk of PRD?
modified 17th July 2024