This is a place where you can talk to others, share your experiences and support one another through your journeys with childhood liver disease.
Blogs are a great way for you to introduce yourself on the forum. You can also comment on other people’s blogs. You may do a one off blog post, or you may choose to do a more regular blog to share your journey.
If you have a question relating to anything about childhood liver disease, use the question facility to ask and others can then answer. You can also answer other people’s questions with your own tips or advice.
If you have any questions, you can contact one of the CLDF admins, Lisa or Laura, who can be identified by the CLDF badge next to their name. You can contact them using the ‘message’ facility within the community or call 0121 212 3839.
If you would like to talk about anything you read on this community, or anything else regarding childhood liver disease, please feel free to call the support team on 0121 212 6023.
For more information on childhood liver disease and CLDF, visit childliverdisease.org
Just confirmed that my son has Biliary artesia 
Hi I am new to this''' I would like to talk to some people who are goin or been through same situation as I am goin through now.
My daughter is 6 weeks post kasai, due to biliary atresia, would like to hear positive things as there is so much negative xxxx
