Erythromelalgia Association, The

Overview

The Erythromelalgia Association (TEA) is an international, all volunteer, nonprofit organization that provides educational and networking services online and offline; raises public 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 of Rare Disorders.

Also called: Eythermalgia, Gerhardt Disease, Mitchell Disease, Weir-Mitchell Disease

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