Free Webinar – “Results of the EDS Awareness World-Wide Survey” – RECORDING AVAILABLE

Watch the recording of this free webinar.

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TOPIC: Results of the EDS Awareness World-Wide Survey

PRESENTERS: John Ferman and Deanna Hamm

John Ferman and Deanna Hamm (father and daughter) are co-founders of the EDS Awareness Program.

There were 2544 respondents to this World-Wide survey from 26 countries. The specific results were presented and discussed during this webinar.

Click IMAGE for the recording of this presentation

Click here for the link to the presentation slides

Click here for the Survey Summary document


  • John Ferman and Deanna Hamm (father and daughter) are co-founders of the EDS Awareness Program.
  • They first introduced the EDS Awareness program at the 2012 EDNF conference and have been sponsors for these conferences for the last 4 years. Will be a conference sponsor in 2016.


The mission of EDS Awareness is to ensure greater understanding of Ehlers-Danlos Syndrome (EDS) by patients, the general public and within the medical community – in order to improve the quality of life for those affected by EDS – and those who care for them.

  • To assist and encourage support groups to organize and spread Knowledge about EDS in their local Communities.
  • To help EDSers locate valuable information, continue to learn,  and to share awareness materials with their EDS peers.
  • To educate patients, healthcare providers and the public about EDS through live webinars held twice a month.


  • Provided free tools and mentoring to help start 100+ EDS Local Support Groups world-wide… and growing
  • Host free EDS educational webinars 2x each month since 2013.  50+ webinars available at our EDS Awareness website


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