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
Always happy to help
Congenital hepatic fibrosis
Weaning to solid foods
7 year old boy diagnosed with Liver Disease
My first little baby has Biliary atresa and I'm so upset and feel so low.Please can I hear anything positive to make me feel a little better
