The Foundation’s mission is to:
• Educate patients and their families about Sjögren’s.
• Increase public and professional awareness of Sjögren’s.
• Encourage research into new treatments and a cure.
How Your Donation Helps
The Sjogren’s Syndrome Foundation, national voluntary health agency. Founded in 1983, the SSF provides patients practical information and coping strategies that minimize the effects of Sjogren’s syndrome. In addition, the Foundation is the clearinghouse for medical information and is the recognized national advocate for Sjogren’s syndrome. The Foundation’s mission is to educate patients and their families about Sjogren’s syndrome, increase public and professional awareness of Sjogren’s syndrome, encourage research into new treatments and a cure.
The Sjögren’s Syndrome Foundation is proud to be the only national non-profit organization focused on increasing research, education and awareness for Sjögren’s.
Address:6707 Democracy Blvd, Ste 325
Bethesda MD 20817
Fill out this simple form or call 1-800-237-5714 to donate.