Family Resource Order Form

Please order CLDF leaflets and packs below. This form is for families, friends and young people.

If you are a medical professional, please use this form here.

If you have any questions or would prefer to order items over the phone, please call us on 0121 212 3839.

Unfortunately we are unable to post any resources outside the UK and Ireland


    CLDF PackGP Practice PackEducation PackFriends and Relatives PackYoung People’s PackSiblings Pack

    Medical Leaflets

    Acute Liver FailureAlagille SyndromeAlpha-1 Antitrypsin DeficiencyAutoimmune Hepatitis After Liver Transplantation (de novo)Autoimmune Liver Disease (Including autoimmune hepatitis and autoimmune sclerosis cholangitis)Baby Jaundice and Liver DiseaseBiliary AtresiaCholedochal CystCongenital Hepatic FibrosisCystic Fibrosis and Liver DiseaseGilbert’s DiseaseHepatitis B (Parents Guide)Hepatitis B (Young People's Guide)Introduction to Liver DiseaseLiver Transplantation – An OverviewNon-alcoholic Fatty Liver Disease (NAFLD)NutritionPortal Hypertension and AscitesPrimary Sclerosing Cholangitis (PSC)Progressive Familial Intrahepatic Cholestasis (PFIC)PruritusWilson’s Disease

    Support Leaflets

    Living without a diagnosisSupport through your child’s liver journeySupporting young people – a guide for parentsJoe's Liver Transplant Storybook (for ages 4-8)Bereavement – A Guide

    Reflection sheets

    MeReasons why I might not go to clinicExploring why I might not go to clinicReasons why I might not take my medicinesExploring why I might not take my medicinesMy Liver - What do I know about my liver?My Liver - Do other people know about my liver?My Liver - Is there treatment?My Liver - Do I need to do something differently?My Liver and Me - What does my liver condition mean to me?My Liver and Me - Does it stop me from doing things I enjoy?My Liver and Me -Do other people understand what it means to me?My Medicines - Do they affect when and what I eat and drink?My Medicines - How do I get my medicines?My Medicines - What do they do?My Medicines and Me - What do I think and feel about taking them?My Medicines and Me - Do they affect how I live my life?My Medicines and Me - Do I need other people to know?My Medicines and Me - Are there any side effects?My Medicines and Me - Do they affect how well I feel?

    Your contact information

    Please tick to give us your explicit consent to process your/your child’s ethnicity details

    Tell Us How You Want To Hear From Us

    Children’s Liver Disease Foundation would love to keep in touch with you about our vital work. By contacting you in the way you choose, we can be more cost effective in our communications and marketing activity.

    What would you like to hear from us about and how?

    Please note:
    1. We don’t send much post so if you only choose one option email would be best.
    2. We’ll update all contact preferences on our systems within 21 days of receiving your request.

    By postBy emailBy phone (a call from a member of the CLDF team)By text/SMS
    By postBy emailBy phone (a call from a member of the CLDF team)By text/SMS
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    We'll always store your personal details securely. We'll use them to provide the service(s) that you have requested and communicate with you in the way(s) you have agreed to. Your details may also be used for analysis purposes, to help us provide the best possible service. We won't sell your details to anyone else and we'll only share them with suppliers working on our behalf, or if required to do so by law. For full details please see our Privacy Policy. It's important that you read this notice to understand what information we hold, how we use it and what your rights are.