Sickle cell disease (SCD) disproportionately affects underserved and historically marginalized communities, where many patients and caregivers have fallen out of regular care, resulting in gaps in treatment continuity.
Our client aimed to re-engage these patients and caregivers to uncover authentic barriers to sustained care to unlock insights that go beyond rational explanations and reveal the deeper emotional, cultural, and logistical factors influencing engagement.
Achieving this required not only careful research design but also trust-building with communities that have historically experienced medical marginalization.