NHF’s annual Washington Days empowers individuals in the bleeding disorders community to impact the legislative process.

Join us to:

• Meet face-to-face with lawmakers and staff who shape national healthcare policy
• Become more informed on critical issues that affect your continued access to quality care
• Learn effective grassroots advocacy techniques
  

Information for Legislators

• Fact sheet: About Bleeding disorders
• Fact sheet: Federal Hemophilia Programs
• Fact sheet: HR 460, the Patients’ Access to Treatment Act
• HR 460: Dear Colleague Letter
• HR 460: The Patients’ Access to Treatment Act (Bill Text)
• About NHF: www.hemophilia.org

Links to Federal Hemophilia Programs:

• CDC National Center on Birth Defects and Developmental Disabilities Division of Blood Disorders
• Hemophilia Treatment Center Directory
• HRSA Maternal and Child Health Bureau National Hemophilia Program

Federal Hemophilia Program Activities

• NHF Programs Supported by CDC Cooperative Agreement:
• HANDI
• Steps for Living
• MentorConnect
• Victory for Women
  
• CDC and HRSA project activities through ATHN:
• HRSA National Hemophilia Program Coordinating Center Factsheet
• National Hemophilia Program Coordinating Center Flyer
• CDC Public Health Surveillance Project for Bleeding Disorders
• HTC Population Profile Flyer