Blog
Meet David Rodriguez, living donor liver transplant recipient and ALF Advocacy Ambassador.
April is Donate Life Month and American Liver Foundation (ALF) is encouraging everyone to learn how to become or find a living organ donor.
Darryl found his niche in life but then liver disease took control and he needed a lifesaving transplant.
The American Liver Foundation (ALF) has begun hosting its annual Liver Life Walks for 2023. There will be 17 in-person walks across the country and one virtual walkheld this year.
We need federal investments for the prevention, treatment, and cure of liver disease to improve the lives of the millions of people affected by it. Read written testimony from American Liver Foundation’s CEO, Lorraine Stiehl, asking Congress to appropriate funding for liver disease research and public health programs within HHS.
Emmanuel Thomas, MD, PhD of University of Miami School of Medicine to lead national board of directors.
A two-day virtual event on March 15th and 16th will bring together key stakeholders with one goal in mind—find solutions to improve health outcomes for all those suffering from rare autoimmune liver diseases.
We applaud President Biden's budget proposal to expand hepatitis C screening, testing, treatment, prevention, and monitoring. We urge the Administration to take similar action for NAFLD.
Jontanna lived the typical life of an American high school student until she was diagnosed with a rare autoimmune liver disease. People like Jontanna need your help, please donate today! Give once or monthly.
Meet Mya Longacre, an ALF patient volunteer who has been navigating her journey with liver disease since birth.
We’re proud to launch our new Pediatric Liver Disease Information Center. Find disease specific information, patient stories, videos, activities, educational resources and more! Access the online site as a parent, teen or child to view age-appropriate information.