Our Vision is a better Wisconsin where EDS and related conditions are fully understood, treated and supported.
EDS Wisconsin, Inc.
EDS Awareness Month Campaign
May is EDS Awareness Month and we have begun our first annual campaign. With your help we can continue to
- Enlighten the public by providing resources and materials to families.
- Inform people through television, print, and online media.
- Update our materials for doctors at medical exhibits, and
- Train doctors and other medical professionals about how to diagnose and treat EDS related disorders.
We are a non-profit organization and your donation is tax deductible. Thank you for your continued support of our mission to provide support and resources to Wisconsin patients and medical professionals about Ehlers-Danlos Syndromes and related conditions via education and research.
Good Morning Tammy. I wanted to tell you from the video you shared with myself and others about mast cells…
Tammy Kosbab, co-founder of EDS Wisconsin, Inc., is extremely passionate about serving patients with Ehlers-Danlos Syndromes and related disorders. Driven…
Disclaimer: 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, Angela Braun, 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.