Raremark Foundation
Sickle Cell Community and Advocacy
Project Description
Sickle Cell disease isn’t a curse. It’s a chronic disease that isn’t getting the coverage it needs. At Raremark Foundation, they got that, and needed to bridge the information gap in society and Uganda as a whole.
Sickle Cell disease isn’t a curse. It’s a chronic disease that isn’t getting the coverage it needs. At Raremark Foundation, they got that, and needed to bridge the information gap in society and Uganda as a whole.
Through a well crafted digital and behavioral change campaign and strategy, we sifted through the noise, delivering expert-vetted sickle cell info through a real-life lens. The impact of which led to the growth of a Warriors community sharing similar experiences and a community of Caregivers supporting each other through knowledge sharing.