By Mara Shapiro from the U.S.
I had the privilege of attending Digestive Disease Week 2022 in person in San Diego at the end of May. I attended the conference as a member of the press for MD / alert (my employer). In addition to attending live sessions, writing articles, and interviewing doctors to create content as a medical journalist for my physician-oriented publication, I was also attending the conference through the lens of an IBD patient advocate.
This was my first time attending a medical conference, and it was a truly eye-opening experience not only professionally but personally. Getting to witness the excitement and gravitas of a major scientific gathering of top gastroenterologists from around the world was thrilling. Meeting fellow CCYAN patient advocates and CCYAN supporters was uplifting and rewarding. It is challenging to find enough adjectives for “excitement” as I describe all the highlights. I was very much like a “kid in a candy store” getting to be a part of the DDW experience.
However, I would be amiss to not mention the imbalance I felt as an IBD patient at a conference focusing so heavily on IBD research and scientific innovation. I, an IBD patient and the subject of most of these sessions and presented research, felt like my experiences were not being accurately represented. I felt lost in a slog of late breaking data and clinical trial endpoints. Where were the patient voices? How come patient narratives were not being presented? Why, in a sea of thousands of IBDologists (as they call themselves on #GITwitter), did I feel so alone?
I have to believe that there is a way to merge scientific discovery and research with patient advocacy, combine the clinician voice with the patient voice, and reach a collaborative understanding of what it means to live with IBD. So often in medicine, the patient’s experience gets forgotten or overshadowed by clinical research and treatment algorithms. Therefore, when patients do get a chance to share their story, it is often given a secondary stage or lesser attention.
What could happen if patient stories were used to aid in the contextualization of all medical research presented at these conferences?
I think we could create a discourse that is not just productive to clinicians and scientists, but that resonates with patients, the very focus and backbone of all this research. We can improve this disconnect. Patients should be able to recognize themselves in the research being presented about their disease.
Advice for clinicians and patients
For clinicians:
Please continue to support patient advocacy efforts such as CCYAN.
Continue to listen to and support your patients and their lived experiences of chronic illness.
Consider implementing more patient-reported outcomes and qualitative measures into your research.
Engage and network with patient advocates at conferences.
For fellow patients:
Continue sharing your story.
Remember that there is room for you at these conferences, and don’t be afraid to find your voice in these settings.