I created this site as a resource for people looking for more information about biliary atresia. Due to a recent diagnosis in my family - see Will - I began scouring the Internet for any information on this previously unknown condition.
Since biliary atresia is so rare - only 1 in 15,000 newborns develop the condition - I was unable to find one consolidated resource, so I decided to build one. For Will when he grows up, and hopefully for others.

I am not providing medical advice through this site. It serves only as a means of consolidating other publicly-available content about biliary atresia. All medical questions should be referred to a qualified medical professional!