Building healthier, empowered communities through care, support, and advocacy.
Our programs address health, education, and empowerment needs of children, adolescents, and caregivers affected by Sickle Cell Disease.
We provide access to screening, clinical referrals, prophylaxis & pain management medications, psychosocial support, and education for families.
Through workshops and community forums, we raise awareness about Sickle Cell Disease to confront stigma in schools and communities.
Training and peer-support groups strengthen caregivers with knowledge, skills, emotional resilience and Economic strengthening initiatives.
Programs for adolescents and young adults (0–24 yrs) focus on mentorship, life skills, and inclusion in decision-making.
Grassroots partnerships with host governments, line ministries, local organizations, co-operates, faith groups and local development partners to expand support within informal settlements and rural areas.
We work with stakeholders to influence health policies and ensure equitable access to care and social services for families affected by Sickle Cell Disease.
We weave in climate change activities into SCD Programing to enhance resilience, improve health outcomes and promote sustainable care of those affected by SCD. Together, we can empower children, adolescents, and caregivers to thrive despite the challenges of Sickle Cell Disease.
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