What we do
Saving Sickle Cell Lives in Rural Africa
We improve the survival, health and well-being of sickle cell patients and their households through access to comprehensive, high quality, timely and affordable care where they live.
How we do it
We design and executes sub-national sickle cell programs in areas of highest need for wholistic Sickle Cell care. We do this in partnership with local government, partners and SCD patients in areas of health policy, health systems resilience, health financing, and patient support.
Our Vision is for a world where all PLSCD have access to comprehensive, high quality, timely and affordable care where they live.
Our Theory of Impact
We hold the view that if PLSCD are provided with early diagnosis, appropriate clinical management and patient-centered care, and if the resilience of the health care delivery systems is strengthened to better care for PLSCD, and if the capacity of the patient’s households is improved to ably care for PLWSCD and improve their overall wellbeing, and if the community, policy and financing environments is created for PLSCD health and rights, then health and wellbeing of the PLSCD will be realized because they will be able to access comprehensive, high quality, timely and affordable care where they live.
