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Bryan was a 22 year old U.S. Marine in perfect health. He was diagnosed with a rare chronic liver disease (Primary Sclerosing Cholangitis).

A routine blood test at an annual physical showed elevated liver enzyme tests. It was then I received an official diagnosis of Hepatitis C.

March 9th 2013 my whole world changed. My liver failed that morning and was diagnosed with Acute Liver Failure and then Cirrhosis at the young age of 30.

They detected “elevated liver enzymes” and encouraged me to be seen by my doctor. This turned into 4 months of lengthy and extensive testing.

In her early thirties, Blum was already struggling to manage not one, but two rare liver diseases: primary sclerosing cholangitis (PSC) and primary biliary cholangitis (PBC).

In 1992, after receiving results from a blood test, Bob Rice learned that he had chronic hepatitis C, a potentially life-threatening disease.

Some of you may already know, today I embark on my most testing journey ever taken, the process of getting placed on the USA organ transplant list – I need a liver.

I’m Becky and I was diagnosed with NASH and was put on the transplant list in 2011. Later in my journey I was officially diagnosed with Cryptogenic Cirrhosis.

Have you ever participated in a Liver Life Walk? If so you may have found yourself walking alongside Art Clark who has been on an 8-year journey as a liver transplant patient/survivor.

Anoura was born on Thanksgiving in 2015. She was a very healthy baby until her skin became yellow and her stool became chalky.

UPMC has partnered with the National Kidney Foundation (NKF) and ALF to educate patients on the liver and kidney waiting lists about the benefits of receiving organs from a living donor.

I am responding with my experience with HE as I was a caregiver for my brother, Javier Nunez, who passed away 8/8/11 due to a brain hemorrhage 3 days after transplant.