American Liver Foundation 2020 Virtual Community Advocacy Training
Every year, the ALF organizes patients and caregivers to go to Washington DC and present our legislative priorities to their Senators, Congressmen, and Congresswomen. It is a powerful experience to step out of the all-to-common silence of liver disease, share our stories, and advocate for positive change. Even more powerful, is to actual see shifts in legislation as a result of our efforts.
This year, we are going virtual with our advocacy and are excited to increase our impact by engaging more advocates than ever! This training took place on September 30th for new advocates who will be taking part in virtual visits October 7, 8, and 9th. While registration for those visits is now closed, we urge you to join us in e-mail campaigns and other online advocacy. Learn more about how the ALF advocates and our legislative priorities in this training video.
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