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.

Education and Support Fund: Education and support are vital to the Foundation's efforts to improve the quality of life for people with Sjögren's. Education ensures that individuals, families, and professionals have the most reliable and up-to-date information, while support programs help people cope with everyday issues of living with Sjögren's.

Research Fund: Research into the causes of Sjögren's, as well as treatments and a potential cure is at the heart of the Foundation's promises to make a difference in the lives of people with Sjögren's and to conquer the disease. Your research donation will help the Foundation speed progress toward a cure by funding the most promising research opportunities and consensus conferences among leading researchers.

If you would like to make a donation to the Foundation, please make check payable to: The Sjogren's Syndrome Foundation

Send to:
6707 Democracy Boulevard Suite 325
Bethesda, MD 20817

To contact the Sjogren's Syndrome Foundation visit: www.sjogrens.org

If you would like to attend the March 18th event, please make your check payable to: "Lynn Arnieri"

Send to:
1318 Fox Glen Drive
St. Charles, IL 60174

Cost: $75.00 per person ($50.00 of each reservation is tax deductible)
Receipts for Income Tax purposes will be forwarded from the Sjogren’s Syndrome Foundation.

All donations will be forwarded to the Foundation and a receipt for income tax purposes will be sent to you from the Sjogrens Syndrome Foundation.