This Talk Clinical Trials blog has been written by Sabrina Poirier, a patient advocate for Myalgic Encephalomyelitis (ME) and other complex chronic illnesses, and co-founder of the ICanCME Research Network. Drawing on her lived experience with ME, Sabrina shares her perspective on how the clinical trials community can better understand and engage with people living with ME.
Many of us living with Myalgic Encephalomyelitis (ME) see research as hope. We count on those in the clinical trials community to help bring safe and well-designed studies to reality – and ideally in collaboration with people like me who have lived experience.
This blog is intended to help you – no matter the role you play in the clinical trials space. Maybe you’re a trialist, on a research ethics board (REB), or a member of a research team. We hope that learning more about ME will help inform your critical work.