I have been doing hepatitis C advocacy for nearly  18  years. My hope and fury have never been greater. We can cure  hepatitis C, but  people are having a hard time getting the medications.  The Centers for Disease  Control and Prevention (CDC) recommends HCV  testing for baby boomers, but we  aren’t doing it. This is the sort of  stuff that drives me wild. 
HCV Advocate  Editor-in-Chief Alan Franciscus asked me if I would  attend “Hepatitis  on the Hill,” held in Washington, DC on March 9 and 10. After  years of  complaining about the government’s anemic response to the hepatitis C   epidemic, I automatically said “yes.”
Approximately 75  hepatitis advocates met in  Washington, DC, for Hepatitis on the Hill. Hosted  by the Hepatitis  Appropriations Partnership, Hep B United and the National  Viral  Hepatitis Roundtable, and supported by the National Alliance of State  and  Territorial AIDS Directors, the event focused on increasing the  federal  response to the viral hepatitis epidemic in the United States.
Hepatitis C virus  (HCV) is  killing more Americans every year than HIV is, but dollar for dollar,   hep C funding is pennies compared to HIV’s. State health departments’  Viral  Hepatitis Prevention Coordinator programs receive less than $1 in  federal  funding for every person living with viral hepatitis. In the  meantime, hep C  infection and death rates continue to rise. Immunizing  all children against  hepatitis B virus (HBV) also continues to be a  problem. 
Advocates from hep B  and C  groups attended Hepatitis on the Hill. The first day focused on core   issues, particularly why now is the time for this level of advocacy.  President  Obama’s budgetary request for viral hepatitis programs is  double that of  previous budgets, and the advocates learned how to ask  for support from their  senators and congressional representatives. 
The next day, advocates visited  the offices of their  senators and representatives on Capitol Hill,  educating their staff on the  experiences of people living with hep B  and C. At each office, the advocates  requested the following:
-                       Signature of  House/Senate  letter in support of the president’s proposed FY2016 budget to  increase  funding of the CDC’s Division of Viral Hepatitis to $62.8 million, and   include the request in the member appropriations submissions  
-                       Support the repeal  of the federal funding ban on syringe services programs 
-                       That their elected  official would join the Congressional Hepatitis Caucus  
Senator Bill Cassidy  (R-LA), MD,  spoke during lunch on Capitol Hill. Cassidy is a hepatologist,   committed to issues surrounding viral hepatitis. Ronald Valdiserri, MD  (deputy  assistant secretary for health, infectious diseases, at the  Department of  Health and Human Services), and John Ward, MD (director  of the CDC’s division  of viral hepatitis), also spoke at Hepatitis on  the Hill. Ward emphasized the  urgent nature of acting now, saying we  can prevent approximately 300,000  deaths. 
Presentations by  Reps. Brett  Guthrie (R-KY), Mike Honda (D-CA), Charlie Dent (R-PA) and Hank  Johnson  (D-GA) were televised at the event. These congressional representatives   introduced the Viral Hepatitis Testing Act of 2015 (HR 1101). In  addition to  being an ally in Congress, Johnson has been public about  his hepatitis C  status, treatment and eventual cure. 
For information about how to  support efforts to improve viral hepatitis funding and services, visit Lucinda  Porter’s blog (
blogs.hepmag.com/lucindakporter).  The National Viral Hepatitis Roundtable and Caring  Ambassadors  Hepatitis C provide ongoing coverage of the latest news and  advocacy  alerts related to viral hepatitis in the U.S.
Portions of this  article by Lucinda K. Porter first appeared in 
Hep Magazine, March 16, 2015.