
Established in 2014, the National Patient Advisory Committee, or NPAC, is comprised of people who are either living with liver disease or caregivers to people with liver disease. These advocates offer their time and energy to further ALF’s mission by generating awareness and providing a face and voice for people impacted by liver disease.
NPAC members are dedicated individuals who undergo a thorough training when onboarded. Training consists of an overview of the American Liver Foundation, a medical overview of the cohort’s disease state, and training segments for media, social media, advocacy and how to conduct ALF’s community education programs- which you will be trained on over the next 5 weeks.
The American Liver Foundation is grateful to the members of our National Patient Advisory Committee. It is our honor to empower them to provide a voice to the voiceless and hope to millions of Americans.