Working toward delivering a significantimprovement in the health and quality of lifeto future generations living with XLHED

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Information for Patients – Resources

Foundations

 

International Patient Registry

The US National Foundation for Ectodermal Dysplasias (NFED) has launched an Ectodermal Dysplasias International Registry and is asking individuals affected by any ectodermal dysplasia to participate. More information can be found here: http://www.nfed.org/research_ed_registry.asp

 

Social Media

Facebook Groups

 

Blog

 

Videos

 

If you know of other patient communities, blogs, videos or resources that you would like to see listed please let us know by emailing info@edimerpharma.com.

Contact Us XLHED Network

Stay informed. Stay connected.
Register for the XLHED Network today.

Current clinical studies

Are you a woman who is a confirmed or suspected carrier of XLHED?
Would you like to be involved in XLHED research? Consider taking this survey www.surveymonkey.com/s/X-CORS

To learn about other studies we are conducting right now visit: clinicaltrials.gov

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