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Lysosomal Acid Lipase Deficiency (LALD)

Lysosomal acid lipase deficiency affects the body’s ability to produce this enzyme needed to breakdown fat and cholesterol. When LAL is missing, fats accumulate and lead to liver and heart disease.

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September 10th is PBC Awareness Day, Know the Facts

Primary Biliary Cholangitis (PBC) Progresses Slowly, Warning Signs Could be Missed.

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Budd-Chiari Syndrome

Budd-Chiari Syndrome is disorder in which veins carrying blood out of the liver become narrow and/or blocked due to blood clots.

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Diagnosing Hepatic Encephalopathy (HE)

Learn if you or someone you love is at risk of getting HE, what triggers this complication and how it’s exhibited.

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Cirrhosis (Severe Scarring)

While fibrosis is reversible there is a point where the damage becomes too great and the liver cannot repair itself. There is no treatment that can cure cirrhosis.

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Primary Biliary Cholangitis (PBC)

Primary biliary cholangitis (PBC) is a chronic liver disease resulting from progressive destruction of the intrahepatic bile ducts in the liver.

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Rare Disease Day 2022: Meet the Kostecki Family

The Kostecki family faced many challenges in discovering daughter Abby's diagnosis of a rare form of liver disease…

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Paysen M.

Her liver enzymes came back elevated. The nurse practitioner wanted Paysen to see a pediatric gastroenterologist.

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PBC Q&A with Dr. Gideon Hirschfield

Dr. Gideon Hirschfield is a leading voice in the field of autoimmune liver disease.

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How Medical Science, a 12-Step Program, and Gratitude Saved Bob’s Life

Bob Rice has packed a lot into his 54 years, but he admits that substance abuse from an early age and then a serious liver disease nearly killed him.

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Billy C.

Several ultrasounds later I was informed that I had an excessive amount of fat on my liver and that my liver was slightly enlarged.

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Natalie Williams

After many visits to the family doctor I was finally referred to a specialist and was diagnosed with Biliary Atresia at 9 weeks old.

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