Research and Advocacy Opportunity – Pancreatic Cancer Ireland Patient and Family Experience Survey

Research and Advocacy Opportunity – Pancreatic Cancer Ireland Patient and Family Experience Survey

Program Name

Pancreatic Cancer Ireland | Patient and Family Experience Survey

Organizer

Pancreatic Cancer Ireland (Patient-led charity)

What is it?

A dedicated patient- and family-led survey evaluating the quality of pancreatic cancer care, treatment access, and support services across the Republic of Ireland. Designed and led by Pancreatic Cancer Ireland, the survey gathers real-world experiences from patients, survivors, and loved ones to highlight system strengths, identify care gaps, and drive meaningful healthcare advocacy. Findings gathered will be presented live at the Pancreatic Cancer Ireland event on 13 November 2026.

Who Should Complete the Survey?

  • Adults living with pancreatic cancer or those who have completed treatment in Ireland 
  • Family members and caregivers supporting a loved one with pancreatic cancer 
  • Bereaved family members who experienced pancreatic cancer care in Ireland 

Geographic Eligibility

  • Republic of Ireland (Focused on the Irish healthcare system) 

Language

  • English

Time Commitment and Survey Features

  • Under 10 minutes to complete.
  • Simple, streamlined online questionnaire designed for ease of participation

Survey Closing Date

  • 13 November 2026 (Responses collected up to this date will directly inform the Pancreatic Cancer Ireland event taking place on November 13th)

Official Survey Link

You can also read: Research and Advocacy Opportunity: European Survey for Young Patients with Colorectal (Bowel) Cancer (DiCE)ghj
DiCE