The local support group is at the genesis of the Foundation and remains its bedrock today. From the first group, started by Elaine K. Harris in 1983, we have grown to sponsorship of over 100 groups located throughout the United States and Canada. These groups, run by volunteers, provide members who have had Sjögren's for some time opportunity to share their advice and tips for living more comfortably with Sjögren's. Each person who attends a support group meeting brings something to it - their experiences about living with Sjögren's, comfort, support, and friendship. Much can be learned at each support group meeting, whether it is a discussion among patients or features a medical professional or other expert.

If you are interested in either joining or starting a support group, please contact the Sjögren's Syndrome Foundation.

One-on-One Support

The Foundation also has local volunteers who can provide support and information by telephone. These contact persons are Foundation members who are knowledgeable about Sjögren's syndrome. They will provide information, education, and support by telephone. We have over 200 contact people.

Contact the Foundation to request assistance and the name of a contact person whom you can call.

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