Sometimes it can be easier to talk to someone outside your family and close friends. CLDF’s Families and Young People’s Teams have a wealth of experience in talking to young people and families who are affected by childhood liver disease. We are always happy to provide information and support but as we are not medically trained we cannot provide medical advice.

How we can help

We are here to support you from the start of your liver journey until your child turns 25. Please view these videos to hear all about what we can offer your family every step of the way. You can also contact a member of the Support Team for specific advice via the staff details at the bottom of the page.

One to one support

Whether you have a specific query relating to your child’s liver condition, or you’re simply feeling very alone and need to talk to someone, we are here for you.  Contact us on 0121 212 6023 from 10am to 4pm, Monday to Friday. If you are not available to talk within these hours, email us at families@childliverdisease.org with your availability and we will do our best to accommodate you.

Kate Conroy

Children and Families Officer/Scotland Support Officer

Our Families team are here to support all families, friends and relatives who may have queries about a child with a liver condition or perhaps just need a chat.

Email: cfofficer@childliverdisease.org or families@childliverdisease.org
Call: 0121 212 6028 or 07533092801

Louise Hawkes

Young People’s Digital Engagement Officer

The CLDF Young People’s Team is here to support all 11-24 year olds.
We meet people at clinics, CLDF events and are here to chat over the phone, on Facebook or WhatsApp.

Email:ypo@childliverdisease.org
Call: 0121 212 6007

Michelle Wilkins

Head of Support

Michelle leads the families and young people’s teams, developing and providing services for children and young people with liver disease and their families.

Email: headsupport@childliverdisease.org
Call: 0121 212 6009