top of page

WELCOME

Erythema Multiforme Association (EMA)

Welcome to EMA. We are here to foster awareness of erythema multiforme (EM) and provide support from those impacted. 

For more information about EMA and our statement of purpose see the above tab "About."

For a discussion of diagnosis, workup, treatments, and publications, see above tab "Medical."

If you have a question and would like to ask our medical board, see above tab "Experts."

To read members' personal stories and for access to the EMA Facebook group, see above tab "Community."

For photo representations of EM, see above tab "Gallery."

Disclaimer: We apologize for the simplicity of our website and lack of links. 

ADVICE DISCLAIMER
Always seek the advice of your physician or other qualified health provider with any questions about your medical condition. Do not disregard professional medical advice or delay seeking advice or treatment because of something you have read here. This information is not intended to be a substitute for professional medical advice, diagnosis or treatment.

©2020 by Recurrent Erythema Multiforme Association. Proudly created with Wix.com

bottom of page