A Local EDS Support Group is a great way to share information and develop “face-to-face” relationships with EDSers having similar experiences.

Watch this free video describing how we can help you start a group and spread local awareness.  Its much easier than you may imagine!

We can show you:

• how to join or start your group
• how to find new members, plan & organize meetings, activities, local awareness, etc.
• how to create your FREE website pages
  (Simple and user-friendly! If you can use a Word processor, you have the skills already!)
• how to get your support group on the EDS Support Group map 

Through local groups and this website community, we will:

• Provide FREE website pages for your group to post meetings, activities, articles, helpful hints, local resources, etc.
• Help EDSers locate valuable information, continue to learn, and create resources to share with their EDS peers
• Participate in 2x per month educational webinars …  https://www.chronicpainpartners.com/webinars/
• Enable you to share your experiences and what you’ve learned about managing EDS, and recommend links to your favorite sites, research papers, books, products, articles, etc.
• Encourage and enable EDSers to inform medical practitioners and the public about EDS