What we do

ASCO improves equitable access to healthcare for sickle cell through action, advocacy and strategic partnerships. These address economic, social and structural determinants of health of people living with and affected by sickle cell disease.

We do this by empowering people living with sickle cell. ASCO equips them with information, resources and skills to understand, manage and thrive with sickle cell.

We strengthen county health systems to respond to sickle cell. Through strategic partnerships ASCO builds capacity of health system and its actors to provide timely, continuous and affordable care for sickle cell at tertiary and primary healthcare levels.

We inform local and national sickle cell policies. Our advocacy efforts and investment in people and systems create sustained impetus for policy and budgetary allocation for sickle cell.

How we do


People

We are building a movement of empowered people living with SCD. Who solve problems, inform systems and policies affecting them locally and nationally. ASCO addresses their determinants of sickle cell i.e.access to health, poverty, stigma, food security and education.


System

People create demand to strengthen health systems in response to this demand. Through county commitments and strategic partnerships, ASCO strengthens health systems ensuring early detection and linkage to continuous care across all health levels.


Policy

Together with communities we work with, we advocate and influence policy locally, to ensure availability, accessibility and affordability of sickle cell care. This is an iterative process that leads to systemic social change.

connect with leaders and government gate keepers

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provide strategic platforms and partnerships

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Advocacy and follow-up

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Sickle Cell

Where we do

Healthcare in Kenya is devolved. But SCD care is centralized in urban areas. Those with most need are unable to access timely, continuous and affordable care.

ASCO co-creates robust sickle cell programs in and with resource poor, high burden, rural communities. We focus on the intersection of people living with SCD, systems and policy responding to sickle cell at local levels.