The Sjögren's Syndrome Foundation, is a 501(c)(3) tax-exempt national voluntary health agency. Founded in 1983, the SSF provides patients practical information and coping strategies that minimize the effects of Sjögren's syndrome. In addition, the Foundation is the clearinghouse for medical information and is the recognized national advocate for Sjögren's syndrome.

The Foundation's mission is to:

• Educate patients and their families about Sjögren's syndrome



• Increase public and professional awareness of Sjögren's syndrome



• Encourage research into new treatments and a cure

Receive updated information in the future or join the Foundation