LC, a worldwide network of lymphoma patient groups, was formed in 2002 and incorporated as a not for profit organisation in 2010. It’s express purpose is to create a level playing field of information around the world and to facilitate a community of lymphoma patient organisations to support one another’s efforts in helping patients with lymphoma receive the care and support needed. The need for a central hub of consistent as well as reliable current information was recognised as well as the need for lymphoma patient organisations to share resources, best practices, and policies and procedures. With this in mind, four lymphoma organisations started the LC. Today, there are 90 member organisations from 55 countries. Vision Equity in lymphoma outcomes across borders. Mission Enabling global impact by fostering a lymphoma ecosystem that ensures local change and evidence-based action.