The Sjögren's Syndrome Patient-Based Registry

The Sjögren's Syndrome Patient-Based Registry is a dedicated database that collects information from people diagnosed with Sjögren's syndrome, an autoimmune condition affecting moisture-producing glands. By gathering data directly from patients, researchers can better understand the disease’s symptoms, progression, and impact on daily life. This helps improve diagnosis, develop more effective treatments, and advance scientific knowledge. The registry also provides a platform for patients to connect, share experiences, and participate in studies, ultimately supporting efforts to enhance care and outcomes for those affected by Sjögren’s syndrome.