Welcome to our Erythema Nodosum Website!

Pronounced: AIR-uh-THEE-ma no-DOSE-um

The purpose of our Erythema Nodosum (EN) Website is to provide you with the most current information regarding EN.

This site consists of informative pages about EN and related illnesses. It also links to sites with information and support for people suffering from EN, along with their friends, family, doctors and medical researchers.

Our Erythema Nodosum Support Group, founded in 2003, is the inspiration for this site. We have combined our own experiences with published research to provide you with as much information on EN as is currently available.

EN is a rare disorder and only a modest amount of medical research has been devoted to it.  We believe that RESEARCH IS THE KEY to finding more effective treatments and an eventual cure for EN.

Imagine life - without EN - and help make that dream a reality!

Please donate generously to the 'Erythema Nodusum Research Fund' through the NORD website at
National Org. for Rare Disorders

and join our EN Fundraiser Support Group to follow 'our' efforts and become active 
in making RESEARCH (and life without EN) a reality.

 

 

 

Site Contents:

Site Main Page

Erythema Nodosum Information

An Invitation For Your Doctor

An Open Invitation To People With EN

Pictures

Panniculitis Information

Auto-Immune Information

EN Triggers

EN Articles and Current EN Treatments Links

EN Related Disorders & useful Health Links

Related Support Groups

Friends Of EN (Link Exchange)

Donation Information

Message from Rebecca Strecker - founder of website and support groups.

Meet Visitors of this EN Website on our Frappr Map
(feel free to click 'Join' to add your location to the Map)