Erythromelalgia Association

The Erythromelalgia Association (TEA) is an international, all volunteer, nonprofit organization that provides educational and networking services online and offline, raises awareness of erythromelalgia, and helps fund research into this rare disorder. Founded in 1999, TEA is funded entirely by donations and is a member of the National Organization for Rare Disorders (NORD). Most functions of the organization are carried out by the volunteer Board of Directors. TEA also has a Medical Advisory Board, a requirement for members of NORD. TEA is proud to have gathered a group of prestigious and dedicated physician researchers to serve as advisors to the organization. Erythromelalgia is a rare vascular disorder characterized by episodes of sudden widening of certain blood vessels (paroxysmal vasodilatation), particularly affecting the skin of the feet and/or hands.