Our Spring 2016 edition of Liver Life is now available covering various aspects of childhood liver disease.
To give it a read, click here.
12 young people attended CLDF’s Talk Tell Transform to share their liver journey.
Our first film features Michael, who was born with biliary atresia...
Booking is now open for our National Conference and Family Weekend, taking place on Saturday 24th and Sunday 25th September 2016.
Find out more here...
Our new social network created for young people by young people living with a liver condition or transplant.
Sign up here!
To help healthcare professionals identify the signs of serious liver disease in newborn babies, CLDF have created the Yellow Alert app.
Are you up for the challenge?
Join our team for the UK's biggest half marathon.
Support CLDF’s work - help us take action against the effects of childhood liver disease
CLDF is here for you. Find out about our events, support services and more.
Research gives hope – learn more about our strategy, grant programmes, news and awards
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