Our mission is to provide support and resources to organizations that provide education, support, research and resources for patients and medical professionals about Ehlers Danlos syndromes (EDS) and related disorders, such as Dysautonomia, Mast Cell Activation (MCA), Autism, persistent pain, and more. Our vision is a better country where EDS and related disorders are better understood, treated, and supported. Since 2017, we have been developing support groups and providing education with EDS Wisconsin, EDS Louisiana, EDS Ohio, and EDS Illlinois. Now that we are officially a 501(c)3 organization, we are looking forward to partnering with and helping to develop more new and/or existing organizations that share our values. Please contact our Executive Director Tammy Kosbab at Tammy@KnowEDS.org if your organization is interested in becoming our partner. Together we are stronger!