The Global Sickle Cell Alliance is a collaborative project aimed at building international partnerships to address sickle cell disease on a global scale. By working with organizations, healthcare providers, and researchers worldwide, we aim to share knowledge, resources, and best practices to improve the diagnosis, treatment, and care of sickle cell disease globally.
The Sickle Cell Community Empowerment Program is designed to strengthen the voices of individuals and families affected by sickle cell disease. This project aims to empower communities through advocacy training, leadership development, and capacity-building initiatives. By equipping community members with the skills and knowledge needed to advocate for their needs, we foster a more inclusive and supportive environment for those living with sickle cell disease.
The Legislative Advocacy for Sickle Cell Care project is at the heart of our mission to transform the landscape of healthcare and support individuals living with sickle cell disease. This initiative aims to influence national policies, secure continuous funding, and prioritize sickle cell as a public health emergency. By advocating for comprehensive legislation, we seek to address the systemic disparities in treatment and care that affect those living with this chronic condition.
