The Sjogren’s Syndrome Foundation (SSF) is a nonprofit organization established to educate patients and their families about Sjogren’s Syndrome, increase public and professional awareness, and encourage research into new treatments and a cure. and Canada. These groups, run by volunteers, provide members with the opportunity to share advice and tips for living more comfortably with Sjogren’s. The SSF offers brochures on Sjogren’s Syndrome, Dry Eye, Dry Mouth, Tips for More Comfortable Living , and a Product Directory listing products available for treating Sjogren’s Symptoms. Serial publication: The Moisture Seekers (newsletter), 11 times a year articles on the many symptoms and complications of Sjogren’s Syndrome, living and coping with Sjogren’s, patient questions and experts’ answers, the latest research, and much more.