Hello, I'm a french woman. I discover your website because my daughter Sara (4 years old now) had biliary atresia and became a new liver in October 2014 (14 months old). I'm interested to know how it works in England and foreign countries. Did your child have a lot of medicines, did they live a normal life ? I have a website about my story with my daughter, but in french 
French experience: Hello, I'm a french... - Children's Liver ...
French experience
Written by
Natacha_Sara
To view profiles and participate in discussions please or .
Not what you're looking for?
You may also like...
STACEY my 2 yr old has PFIC
Hi All xx
This is my first time here, I won't go into all the details but my 2 yr old daughter has...
Portal hypertension, enlarged spleen and liver damage
Can anyone give me any advice on portal hypertension, my 1 year old daughter has Biliary Atresia,...
7 year old boy diagnosed with Liver Disease
I'm devastated. Today I was told my 7 year old son has Liver disease. Despite a few issues he seems...
biliary atresia
Hello everyone,my daughter is 6 months old,has biliary atresia,awaiting liver biopsy results ,what...
Biliary atresia
Hi everyone, my name is Louise Currie, I was born with Biliary Atresia and was given the kasai...
Related Posts
Billirubin levels in patients with alagille syndrome 
Biliary atresia 
My daughter is 6 weeks post kasai, due to biliary atresia, would like to hear positive things as there is so much negative xxxx
Suggestions on how to include my 3 year old now my baby has been diagnosed with biliary atresia please?
1 week passed after kasai
