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).
Lydia had no idea she was born with a chronic autoimmune liver disease until one day she found herself desperately fighting for her life. She is now on a mission to help spread awareness about the importance of liver health an early detection, and to encourage lawmakers to increase federal funding for the study of liver disease research. Read Lydia's story now!
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.
After being diagnosed with nonalcoholic fatty liver disease (NAFLD), Manny learned all he could about the disease, including how the prevalence of NAFLD is higher in U.S. Hispanic populations. As a second generation Mexican American, Manny is on a mission to raise awareness in the Hispanic community and encourage people to get screened before it is too late. Read Manny’s story now.
American Liver Foundation (ALF) announced new liver research awards for 2024 that will fund early career scientists interested in basic and translational research.
After experiencing the gaps in health equity firsthand, Evelyn, a two-time liver transplant recipient and proud multi-generational New Mexican, advocates to raise awareness of liver disease and increase access to liver healthcare and transplant in minority and rural populations.
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.