Patient Stories

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Natalie Williams
April 20, 2020

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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Millie T.
April 20, 2020

I was born with BA and had two surgeries before the age of one. I had no idea why I had these scars and went on with life.

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Meiyee C.
April 20, 2020

After taking her to American Family Children’s Hospital in Madison at the beginning of the summer, they learned she had biliary atresia, which meant the bile ducts from her liver were not formed.

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Matt R.
April 20, 2020

Our doctor instantly recognized Matthew’s jaundice as the indication of a possibly serious condition.

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Noel R.
April 20, 2020

When she was just two months old, Noel was diagnosed with a liver disease called Biliary Atresia. Her parents were devastated when she had to undergo surgery to clear her bile ducts.

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Nick W.
April 20, 2020

Diagnosed with biliary atresia at only two weeks old and receiving his first surgery at three and a half weeks, Nick ultimately needed a liver transplant when he entered adolescence.

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Andrew
April 17, 2020

Our son Andrew was born September 30, 2013 with a genetic liver disease called Alagille Syndrome. At 8 days old we started seeing a liver specialist at Children’s of Alabama.

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Aiden
April 20, 2019

The doctor called and advised her that he suspected Biliary Atresia. He explained that it is a rare, life-threatening disease that affects the liver in newborns.

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Tom N.
November 14, 2017

Tom signed up to join a Run For Research Team and compete in the Boston Marathon. This is where he met Zac Rue, a little boy living with Biliary Atresia.

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