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Ehlers-Danlos National Foundation
appreciates your support! 
Ehlers-Danlos Syndrome (EDS), is an incurable and often disabling connective tissue disorder which affects approximately 1 in 5,000 people. Its' complex symptoms can be devastating and lead to isolation and frustration by its' sufferers due to the lack of medical awareness. By leading the search for knowledge about EDS, the Ehlers-Danlos National Foundation (EDNF) is building a community of people who work together to effect change. EDNF does this by: * Creating and distributing accurate information * Providing a network of support and communication * Fostering and funding research. EDNF has grown from one woman's grassroots efforts into a vital information link to and from the medical community. EDNF, its member volunteers, Board of Directors and Professional Advisory Network strive to support research and education in an effort to prevent crippling disfigurement and premature death through early and accurate diagnosis. EDNF is completely dependent upon charitable gifts and membership dues. Thank you for purchasing the hCard and for your support of EDNF! http://www.ednf.org
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