Sharing the Journey, an ALF support network for Caregivers
The American Liver Foundation offers this support network for people who are caregivers for loved ones with liver disease or who have had or need liver transplants.
The American Liver Foundation offers this support network for people who are caregivers for loved ones with liver disease or who have had or need liver transplants.
Being diagnosed with a genetic liver disease can be overwhelming, and understanding your condition can be a challenge. This webinar offers some guidance and education on the causes, symptoms and diagnoses of primary biliary cholangitis (PBC) and primary sclerosing cholangitis (PSC) along with updates on the latest research and treatment options.
The American Liver Foundation offers this support network for people who have been diagnosed with liver disease and those who are awaiting liver transplant. Liver disease can pose many unique challenges, both physically and emotionally.
Join us for our monthly Young Leadership Council meeting. Meet other young professionals, expand your network, get involved, and help make a difference in the lives of the 100 million Americans affected by liver disease.
This group is for people who have received liver transplants and wish to connect with other transplant recipients.
The Liver Health ECHO Program is a virtual community of practice developed to equip providers with the necessary skills to treat and prevent NAFLD among their patients.
The American Liver Foundation offers this support network for people who are caregivers for loved ones with liver disease or who have had or need liver transplants.