As a Sjögren’s patient, you face the challenge every day of coping with this debilitating disease. Though there are an estimated four million Americans living with Sjögren’s syndrome, you often feel alone and are unable to find credible information.

That is why, twenty-five years ago, the Sjögren’s Syndrome Foundation began its crusade to serve as a resource for Sjögren’s patients. Whether you are newly diagnosed or have been suffering with Sjögren’s for years, we hope that you will use this website as an excellent source of information.

Inside sjogrens.org you will find information on:

• Living With Sjögren’s Syndrome.
• Frequently Asked Questions about Sjögren’s syndrome.
• Support Groups where you can connect with other patients.
• Registering for our Patient Seminars and National Patient Conferences.
• How to get involved with the Foundation.
• Ways to increase awareness of Sjögren’s syndrome.

Additionally, if you become a member of the SSF you will also have access to the following:

• Discounts on Sjögren’s resources and registration costs for Patient Seminars and National Patient Conferences.
• A monthly subscription to our newsletter, The Moisture Seekers.
• Archived articles from the monthly newsletter.
• Access to our Member Community – where you will be connected with other Sjögren’s patients.

If you have any questions or want to contact the Foundation, please call us at 1-800-475-6473. Remember, you are not alone. The Sjögren’s Syndrome Foundation staff and volunteers are working on your behalf to conquer Sjögren’s syndrome.