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Patient Voices in Research: Elaine’s Das Cheppo Journey with iPROLEPSIS

Mar 4, 2025

A Patient’s Perspective: Elaine’s Journey with iPROLEPSIS

Elaine Das Cheppo has been living with psoriatic arthritis for 25 years. Like many others, her diagnosis was delayed, making treatment more challenging in the early years. When her rheumatologist asked if she would like to take part in the iPROLEPSIS project, she did not hesitate.


"I struggled in the beginning to understand why I was experiencing so much joint pain. By participating in this study, I hope to help future generations get a diagnosis faster than I did."


The Role of Patient Partners in iPROLEPSIS

Elaine is a patient partner in iPROLEPSIS, working alongside researchers to improve psoriatic arthritis care. She finds the co-creation sessions particularly insightful, offering her a behind-the-scenes look at how digital health solutions are developed.


"It’s interesting to see how new technology is being used to improve diagnosis and treatment. These innovations could help people avoid unnecessary doctor visits and manage their condition more effectively."


A Renewed Sense of Purpose

For Elaine, being part of iPROLEPSIS is not just about contributing to research—it’s also about personal fulfillment.


"For someone who has been retired for quite some time, it’s rewarding to have a new goal and interest in life. Being part of this project gives me a way to make a difference."


Watch Elaine’s full story here:



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