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Ehlers-Danlos National Foundation

 

EDS Awareness has been a sponsor at the annual EDNF/EDS Learning Conferences since 2012. You will see our logo on the EDNF/EDS Sponsor page.

At the conferences we discuss forming local EDS support groups and provide information about our 2X monthly live EDS Educational Webinars and EDS Awareness activities in local communities.

Check out the links above.

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Upcoming

Webinars Schedule

Susannah Fox

Live Webinar with Susannah Fox, Author of Rebel Health

Karina Strum

New Feature-Length Ehlers-Danlos Documentary ’We Are Visible’

See full schedule

Webinars

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The mission of EDS Awareness is to ensure greater understanding of Ehlers-Danlos Syndrome, both in the general public and within the medical community. Driven by participation and shared learning, we hope to improve the quality of life for those afflicted with EDS – and those who care for them.
Website content is presented “by EDSers, for EDSers” – therefore, it is driven by user participation and learning – for the benefit of all EDSers. The greater the participation, the greater the value to the whole community.

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