Children’s Liver Disease Foundation was set up in 1980 by a family whose child sadly died.  Over the years the charity has grown dramatically and continues to make a real difference in the paediatric liver world in the UK.  CLDF promotes research into all aspects of childhood liver disease; provides emotional support; is the voice for babies, children, young people and their families and adults diagnosed in childhood; and provides effective information programmes and create a greater awareness of childhood liver disease.  With all of this in mind; CLDF also continues to place huge value and importance on its children who are sadly no longer with us.

CLDF's support does not end when a child dies, so please use this page to remember someone special to you, whether a son/daughter, brother, sister, friend or someone you spoke to a few times when you were on the ward or at a hospital visit – this tribute fund is a place for you. Light a candle, write a tribute, make a contribution to CLDFs vital work - However you want to use this tribute fund, please feel free. 

CLDF’s bereavement service includes:

A range of literature for you and other children in your family

A memory book in which your child’s name is honoured. The book is displayed atCLDF’s offices in Birmingham and is taken to certain events.

A specially designed journey box for your child’s precious mementos

Set up a personal Sunshine Tribute Funds - to honour the memory of a loved one

Our next Remembrance and Celebration Service will take place in 2017

The National Memorial Arboretum is home to the CLDF tree in memory of the livesof children and young people lost to childhood liver disease

The CLDF's Families Team are always here for you. Should you wish to get intouch please contact us on 0121 212 6023 or email families@childliverdisease.org