National Health Insurance

Access to treatment for Hemophilia is life-saving and should be supported through national health insurance schemes and public health systems.

Goals

• Ensure access to factor therapy and diagnostics
• Cover physiotherapy, home care, and orthopedic services
• Prevent catastrophic out-of-pocket expenses for families

Advocates can work with governments to include Hemophilia under rare disease coverage, essential medicine lists, and disability protection laws.