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Welcome to EDS Today.

EDS Today is the newsletter for, by, and about people with Ehlers-Danlos Syndrome.

NEWS FLASH

To All Our Supporters,

We have relocated once again, our office is now centered in New Jersey. Our new contact information is listed below. We'll be posting a letter shortly explaining everything that has happened over the past year. We thank you for your continued patience and support during this time.

Sincerely,
The Board of Directors

Mission Statement:
The mission of EDS Today is to provide information and support to people living with EDS, their families, and the medical community. Ehlers-Danlos Syndrome is a group of six genetic connective tissue disorders.

EDS Today is a 501(c)3 non-profit organization. We are 100% staffed by volunteers. All donations to EDS Today are used to support EDS Today's mission.

Information provided in articles are the opinions of the writer and are not to be construed as the opinions or beliefs of the editor or EDS Today staff. It is our goal to provide an informative open-forum for ideas, information, and support for people with EDS. For more information, please read our full disclaimer.