Parents



How CLDF Can Support You and Your Child

 

If your child, or a child in your family, has a liver disease, it’s very easy to feel like you’re alone. You’re not. CLDF is here for you and we’ll be with you every step along your journey, wherever that may lead.

Our family services start with providing essential medical informationWe also have practical information on living with liver disease which will help you cope, especially in the early days.

Our Families Team are here for you by telephone, email, text or Facebook and they would love to hear from you. You can also meet them when they visit the liver clinic – to see the CLDF Hospital Visits Timetable please CLICK HERE. 

If we haven’t already met you, or you don’t already receive information from us, please CLICK HERE to tell us all about you and your family.

We can also put you in touch with other families in your situation through our family events and our online community.

Families tell us how they benefit from learning about the experiences of others – you can see stories from other families affected by childhood liver disease and have the opportunity to share your own story.

We’re also here for your wider family and friends who may want to know how they can help you and your family.

We have a dedicated service for young people with liver disease, including a Young People’s Digital & Engagement Officer, secure social media platform, special events and residential trips.

Our Families Team can be contacted on 0121 212 6023 or 07528 063636, by email at: families@childliverdisease.org or via Facebook.