The Kamara Sickle Cell Project (KaSP) is an initiative committed to raising awareness of Sickle Cell Disease (SCD) in Liberia while empowering individuals living with the condition and their families through advocacy, support, and access to essential resources.
Founded by Karen Kamara Schaack, a warrior and advocate living with SCD herself, KaSP was inspired by her late mother of three sicklers, Mary sia Kamara; and is driven by lived experience and a deep understanding of the challenges faced by those affected. Through its work, KaSP seeks to illuminate the realities of SCD, breaks the silence around the disease, and fosters a more informed, compassionate, and supportive community across Liberia.
MTS Sickle Cell Foundation, Inc.
My Three Sicklers
MTS Sickle Cell Foundation has spent over a decade empowering and supporting individuals living with Sickle Cell Disease (SCD). Dedicated to improving the lives of warriors and their families, the foundation provides critical resources through financial assistance, education, community outreach, and policy advocacy. With a mission to ensure that no warrior fights alone, MTS continues to drive meaningful change in the SCD community.