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Thank you for supporting EDS Wisconsin in whatever way you can–and there are many. Your support through monetary contributions, event attendance, social media presence, supporting patients through mentorship and listening, following our blog, and even just by having an awareness of our experience with...
read MoreNovember 24, 2023
November 14, 2023
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May 4, 2020
Help us to provide support and resources to Wisconsin patients and medical professionals about Ehlers-Danlos Syndromes and related conditions via education and research.
Cash donations are the most helpful. Below is a list of items that we currently need. To make a donation, please contact us using the form below, and we will get in touch with you as soon as time allows. Thank you.
President and Founder of EDS Ohio, Kassady Oberacker is both an EDS advocate and patient living in Cuyahoga Falls, Ohio. Her background is in Applied Conflict Management and Psychology from Kent State University and...
Current city: Madison Profession: Designer and Retail Manager Education: Attended the Milwaukee Institute of Art and Design, earning a BFA in Illustration.
What people are saying about us…
Being part of this team has become something unexplainable. I’m a part of something great, and it’s so much bigger than me. It is a cohesive unit. I am in awe! The help we give others goes directly to the person in the other side. It’s real real life and I love it!
Volunteer with EDS Wisconsin
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Great resource for people with EDS in the Wisconsin area!
Crystal Lindell
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I wanted to tell you from the video you shared with myself and others about mast cells I could understand it from how you did your presentation. I have in the past read articles cut I came away more confused. But how you explained it made it easy to understand. I am looking forward to seeing more videos from you! You have a special way of explaining these difficult subjects & you’re helping so many of us with your knowledge <3
Sally Orlowski, .
Tammy Kosbab is a dedicated individual who has seeded and grown this organization at an incredible rate in it’s first year and continues to keep the pace. The amount of information, resources, people and live interaction to support and educate those affected with or by EDS and related illnesses and syndromes is extraordinary. Her ability to network and build this first rate educational non-profit is admirable. EDS Wisconsin, Inc. is bound to be a world class organization.
Deb Klecker, .
Any question our family has had, has always been answered. This is a judge free zone full of people who want to help one another.
Kathy Vandersteen, .
Most helpful support group ever, not just the ppl although their wonderfully warm, but I’ve come away from the meetings with so much more knowledge, referrals & resources! They’ve helped me connect the dots about what’s going on with me, find specialists to help me and best of all I know that I’m not alone in this journey. Some of the ppl I’ve met at the meetings have so much in common with me that I hope we’ll be life long friends supporting each other in the struggle with this rare syndrome!
Gracie Murbach, .
This is so great! I really appreciate all the time you put into helping me be my best leader and a better person for myself and a support for others. People look to me for that now and it’s such a wonderful and awesome responsibility. I understand the gravity of it and take it seriously, even through my goofy sense of humor.
Michelle Stevens.
EDS Wisconsin is very helpful-excellent resources, knowledgeable leaders, assistance finding EDS aware providers, excellent support groups and much more. Finding peer support is enormously beneficial. Knowing that others understand your circumstances and support you is invaluable. It is an honor to know the members and leaders of this organization. ???
Stacey Slottey.
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