Children’s Liver Disease Foundation held its National Conference and Family Day on Saturday 6 October. The afternoon consisted of four parallel sessions covering various topics.
Helen Pattison’s presentation focused on ways to communicate and share information with your child surrounding their liver condition. The session identified a number of issues for discussion;
How much information should you give your child?
What questions does your child ask about their liver disease?
What do your other children ask about liver disease? How much do you tell them?
Do you make clinic appointments a special outing or is it part of normal life?
Do you let your child know about having a procedure like blood tests or is it just sprung on them?
Feel free to respond to these questions and join in the conversation...