Introduction
Thank you for taking the time to complete this survey.
We want to understand your experience of pancreatic cancer care in Republic of Ireland, from first symptoms through diagnosis, treatment, support services, and communication with healthcare professionals. We ask that only those who experienced pancreatic cancer care in the Republic of Ireland take part in this survey.
This survey is open to:
- People living with pancreatic cancer
- People who have completed treatment
- Family members supporting someone with pancreatic cancer
- Bereaved family members whose loved one had pancreatic cancer
- People who have completed treatment
- Family members supporting someone with pancreatic cancer
- Bereaved family members whose loved one had pancreatic cancer
The purpose of this survey is not academic research. It is a patient led survey that aims to identify what is working well, what is not working well, and what needs to change.
The information gathered will help inform our discussions and advocacy priorities at our November meeting, ensuring that the voices and lived experiences of patients help shape the conversations and decisions that affect them.
Your experience matters, and every response helps build a clearer picture of pancreatic cancer care across Ireland.
Your privacy is important to us. Survey responses will be used to help us understand patient experiences and identify areas where change is needed. The findings will be shared with delegates attending the Pancreatic Cancer Symposium in November to help inform discussion and support our advocacy for meaningful improvements in pancreatic cancer care and support. Responses will be stored securely, and findings will be presented in a way that protects the privacy of individual participants. Please avoid including names or other identifying information in your responses.