The AGS Alliance is an international support network for people with AGS (Alagille Syndrome), a rare genetic multi-symptom condition, and their families. We are run by an all volunteer Board of Directors composed of dedicated, committed individuals whose lives have been touched by AGS. We recognize the wealth of knowledge that is gained through research and encourage AGS families to participate in studies so that they may contribute to the growing information base about this disease. We are here to answer questions, provide sound information, and lend a sympathetic ear as families enter the world of AGS and the challenges it presents throughout one's life.