Blog
The American Liver Foundation (ALF) is proud to once again be a member of the Bank of America Chicago Marathon Official Charity Program for the 2024 race, which takes place on Sunday, October 13, 2024, starting in iconic Grant Park.
Facing liver disease as a child can be a lonely process for both kids and parents alike, but not anymore. American Liver Foundation (ALF) is proud to announce the launch of Bili the Brave™ for children and families affected by biliary atresia (BA).
Take a liver health quiz, try a new 30-day liver healthy meal plan, and participate in free educational and community events all month long!
The American Liver Foundation (ALF) is proud to be a member of Charity at the BMW Berlin Marathon for the 2024 BMW Berlin Marathon, which takes place on Sunday, September 29, 2024. This will be the 50th anniversary of the prestigious event.
The Balm Box, a leading online retailer of premium care packages designed for cancer patients, announced a new collaboration with American Liver Foundation (ALF) today.
The ALF National Legacy Gala on October 7, 2024, at Gotham Hall, NYC, will bring together patients, families, thought leaders, medical professionals, business visionaries, and partners to celebrate impactful contributions to the liver community, raising awareness and funds for liver disease.
This Sunday, September 8th, is International PBC Awareness Day and American Liver Foundation (ALF) is encouraging everyone to know the facts and warning signs of this autoimmune liver disease.
American Liver Foundation (ALF) announced new liver research awards for 2024 that will fund early career scientists interested in basic and translational research.
Liver disease affects more than 100 million Americans, yet federal investment in early diagnosis, prevention, treatment and research continue to lag far behind other chronic diseases. This summer, American Liver Foundation (ALF) advocates will meet virtually and in-person with elected officials in their local cities and towns to share their liver stories and lend their voices to urge action.
American Liver Foundation (ALF) announces a new Project Echo program for healthcare providers that will bring treatment and prevention best practices for nonalcoholic fatty liver disease (NAFLD)* to non-liver experts.
American Liver Foundation (ALF) announced the first-ever patient registry for all types of liver disease. The American Liver Foundation Patient Registry will help provide researchers with a better understanding of liver diseases, the impact of current treatments, and how liver disease affects patients.
American Liver Foundation (ALF) announces a new peer support program to help those living with or caring for someone with any type of liver disease, including transplant, connect with others facing the same challenges.