TEA works to add to and maintain the information contained on this website to educate those with Erythromelalgia symptoms, and their doctors, family, and friends.
TEA’s A Patient’s Guide to Erythromelalgia was created and published for the first time in Spring 2016. This guide is a comprehensive description of many aspects of the disease, from symptoms and diagnosis to treatment and daily coping tips. It is a unique tool that those with EM (and their families and health care providers) should have at their fingertips as they strive to improve their lives in regard to EM.
TEA has compiled a list of answers to frequently asked questions regarding EM. The information contained within the FAQs is intended for generalized and educational information only.
Explore TEA’s collection of medical articles pertaining to treatment, research, general information, and EM/Raynaud’s.
The doctors and researchers listed in the Physician Directory have been suggested by TEA members over time. TEA does not recommend or endorse any of these doctors or researchers.
For the second time in TEA’s history a member/patient survey has been conducted.
In 2021, The Erythromelalgia Association (TEA) conducted a survey among TEA members and others with eythromelalgia. More than 680 individuals responded and completed the full survey.
In 2008, TEA distributed its first comprehensive survey to its members, covering questions on symptoms, treatment, and diagnosis among other issues. Of the approximately 650 surveys that were sent, the survey elicited 427 responses, approximately 66%!