The Mission of EDS Wisconsin, Inc is to provide support and resources to Wisconsin patients and medical professionals about Ehlers-Danlos Syndromes and related conditions via education and research.

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Our Vision is a better Wisconsin where EDS and related conditions are fully understood, treated and supported.

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EDS Wisconsin, Inc.

Strengthening Connections!


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More information about EDS Wisconsin will be coming soon!

Learn about our Board Members here.

Learn about our support groups!



EDS Wisconsin, Inc. is not a health care provider and does not provide medical advice or treatment. Information provided by EDS Wisconsin is not a replacement for care from a doctor or other health care provider. Please talk with your health care provider about your personal diagnosis and treatment options. All information contained within the Support Group is for educational purposes only. All contributors, including EDS Wisconsin, Inc., Linda Bluestein, Tammy Kosbab, Steve Swierczynski, Tsilos Schoener, EDS Wellness, EDS Network CARES, Christine Quackenboss, Dawn Dembosky, Deb Klecker, Beth Wroblewski and others cannot be held responsible for misinformation, misconduct or malpractice.  Information provided is not a substitution for medical care or advice. 


Next Steps…

If you are interested in the opportunity to help make a difference with EDS Wisconsin, please fill out this Volunteer Application.

Subscribe to our mailing list here.

Like us on Facebook!

Find out more about the regional support groups here: Madison, Milwaukee, Wausau, Green Bay/Appleton, Eau Claire, and Ashland/Duluth (coming soon!).

Join the Madison Support Group here.

Join the Online Support Group Meetings here.

Join the Kids & Teens Support Group here.

Join the Milwaukee Support Group here.
Join the Wausau Area Support Group here.
Join the Eau Claire Area Support Group here.
Join the Green Bay/Appleton Area Support Group here.

Interested in becoming a partner, sponsor, donor or contributor? Click here!