A Seat at the Table: The Power of Patient Advocates in Innovation
From “Subjects” to Stakeholders Not long ago, people living with diabetes were seen primarily as recipients of care, (royal?) subjects of studies. We were “just” individuals to educate, treat, and monitor. Decisions about technology, policies, and priorities were made for us, not with us. #nothingaboutuswithoutus ! But something is shifting, even if ever so slowly. […]
