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About Sjogren's Australia

Dry eyes. Fatigue. Pain. Isolation. For too long, Australians living with Sjögren’s disease have felt invisible. Sjögren’s is a serious, systemic autoimmune disease impacting the body far beyond “just dry eyes and mouth.” It can attack organs, joints, nerves, and shatter lives. Yet despite affecting an estimated 1 in 300 Australians, it remains drastically underdiagnosed, under researched, and misunderstood. That’s why Sjögren’s Australia was born. Founded by patients and advocates determined to change the future, we are a national not-for-profit dedicated to transforming the lives of Australians affected by this complex disease. We exist to raise awareness, accelerate research, and improve access to treatments and support, driven by the real stories of people who live with Sjögren’s every day. Our vision is bold: To see patients' lives transformed by science, support, and connection until we reach a cure. We work alongside medical experts, researchers, families, and allies to push for change at every level from Parliament House to your local GP clinic. Through advocacy, education, community-building, and funding research, we are shining a light where there was once darkness. We’re here to lead the conversation, not wait for it. Join us whether you’re a patient, health professional, policymaker, or supporter. Together, we’ll make Sjögren’s visible.

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