Little Hearts Matter offers support and information, and raises awareness of those affected when a child has only half a heart, due to conditions such as Hypoplastic Left Heart Syndrome. A number of families sadly lose a child to complex heart disease and so over the last few years they have been working to develop a support service for families whose children have died. Run by the Bereavement Support Team and the LHM office they try to offer families the opportunity to talk to other families whose experience is similar to their own. They offer someone to link to either over the phone, via email or at one of their bereavement support events. If you would like to talk to other parents who have lost a child due to complex congenital heart disease, either visit their Bereavement section on the Message Boards or you can call the office to be put in contact with one of their Bereavement Support Team.