The Global Action Network for Sickle Cell & Other Inherited Blood Disorders (GANSID) as a collective works to improve the health outcomes of people affected by hereditary blood disorders (HBDs) regardless of where they live in the world. It strives towards equitable access to care by connecting regions, nations, localities, partners, and people to effectively advocate for and improve care infrastructures for All people living with hereditary blood disorders.
The GANSID will shape and advance disease-specific and cross-disease, global, regional, and national advocacy initiatives. It will enable the advancement of shared priorities through unified and coordinated data-driven advocacy.
The GANSID will also support the creation of national registries for hereditary blood disorders.