Blog
A lot is happening in Washington DC, so the ALF team will draft a weekly health policy round-up to keep you up to date and informed.
ALF’s Liver Life Advocacy Summit was held in Washington, D.C. April 29th and 30th and brought together patients, caregivers and families from coast to coast to champion legislative priorities for liver health and help the 100 million Americans affected by some form of liver disease.
Jenna never let liver disease keep her from showing up for her husband and three young boys, in fact, they gave her the motivation to fight even harder. Now, after nearly losing her life, Jenna is on a mission to create positive change for all those affected by liver disease. Read Jenna's story now.
A lot is happening in Washington DC, so the ALF team will draft a weekly health policy round-up to keep you up to date and informed.
American Liver Foundation (ALF) will bring together patients, caregivers, and family members affected by liver disease from across the country for the Liver Life Advocacy Summit in Washington, D.C., on Tuesday, April 29 and 30 to champion ALF’s 2025 legislative priorities.
A lot is happening in Washington DC, so the ALF team will draft a weekly health policy round-up to keep you up to date and informed.
ALF anuncia el primer registro de pacientes en español para todo tipo de enfermedades hepáticas para ayudar a garantizar que las necesidades y experiencias de la comunidad hispana/latina se incorporen a los datos que pueden ayudar a conducir a futuros tratamientos y curas para la enfermedad hepática.
ALF announces the first-ever Spanish-language patient registry for all types of liver diseases to help ensure that the needs and experiences of the Hispanic/Latino community will be incorporated into the data that may help lead to future treatments and cures for liver disease.
A lot is happening in Washington DC, so the ALF team will draft a weekly health policy round-up to keep you up to date and informed.
Unleash your inner foodie and experience a distinct evening of dining all for a good cause. Funds raised benefit the 100 million Americans affected by liver disease through resources, education and support services and help advance our advocacy efforts on Capitol Hill and liver disease research.
Bill silently developed alcohol-associated liver disease over three decades of alcohol use disorder. After finding himself in need of a lifesaving liver transplant, he dedicated his second chance to raising awareness about the risks of alcohol, and to helping those in recovery heal and overcome negative stigma. Read Bill's story now.
American Liver Foundation (ALF) is proud to announce a new living donor network to connect those wishing to donate part of their liver with transplant centers to help patients in need.