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My name is Carolyn Evans and I was diagnosed with Primary Biliary Cholangitis (PBC) in 1992.

Biliary atresia is a disease of the bile ducts that affects only infants. It is rare, affecting about one out of every 18,000 infants.

I was diagnosed with PBC at the age of 43. I suspect that I had it long before that as I had already been diagnosed with Hashimoto’s Thyroiditis and had been told I had high liver enzymes.

Liver cancer strikes 33,000 Americans annually, according to the American Cancer Society and it is expected that 23,000 Americans will die as a result of liver cancer this year.

Approximately 6,000 liver transplants are performed in the U.S. each year. But more than 17,000 Americans are still waiting for donated livers to become available for transplants.

ALF asked Dr. Boyer to share his perspective on improved prospects for PBC patients and their challenges to effective treatment.

Test your knowledge about liver disease and learn more about what fatty liver disease is…

My story begins with a diagnosis of Primary Sclerosing Cholangitis. After the diagnosis, I required numerous stents to be placed in my bile duct through a procedure called an ERCP.

My name is Danielle and I am a 26 year old biliary atresia survivor from Staten Island, NY.

During surgery my doctor discovered I had cirrhosis of the liver. I had PSC (Primary Sclerosing Cholangitis). This is when bile ducts in the liver are clogged or closing.

After ten days in the hospital and an ERCP (a scope of the bile ducts), they diagnosed me with PSC. The ERCP showed that my bile ducts were narrowed and the bile was being blocked.

I was diagnosed with Nonalcoholic Fatty Liver Disease (NAFLD). It was a huge shock to me since I never had any major health issues.