Blog
Stacey became involved with ALF after attending a caregivers’ program at the hospital where her partner, Zach was diagnosed with end stage liver disease.
“Twenty-five years ago, while I was pregnant with my daughter, I turned yellow. Doctors told me my jaundice would get better after I delivered my daughter. That did not happen.” Read Danae’s story about living with an undiagnosed liver disease.
On behalf of nearly 100 million Americans affected by liver disease, we applaud the reintroduction of the Living Donor Protection Act of 2023.
ALF will become the first liver organization to join AST’s Living Donor Circle of Excellence and become a strategic partner.
Meet Melissa Sanchez – a dedicated volunteer and passionate advocate for the American Liver Foundation (ALF). Melissa said, “I advocate in memory of my grandmother, Aira Sanchez, who bravely battled end stage liver disease from 2012-2014.
Read how this year’s marathon is extra special for two marathoners running for their dad who will receive a life-saving liver transplant!
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.