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:
An Open Invitation To People With EN
EN Articles and Current EN Treatments Links
EN Related Disorders & useful Health Links
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)
