Sjögren's Foundation

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The Latest From the Sjögren’s Foundation

New Patient-to-Patient Story: Neurological Issues, Carmen's Story
Dec 8, 2023
Women's Health Research Initiative
Nov 30, 2023
Sara McCoy, MD, PhD, Recognized by the NIH Leadership Scholars Program to Further Sjögren’s Research
Nov 9, 2023
New Blog! Revamping the Foundation Research Policies to Improve the Future of Sjögren’s
Nov 6, 2023

What is Sjögren’s?

Sjögren's is a systemic autoimmune disease that affects the entire body. Along with symptoms of extensive dryness, other serious complications include profound fatigue, chronic pain, major organ involvement, neuropathies and lymphomas.

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Our Impact

Advancements in Sjögren's research and increased awareness for Sjögren’s speak to the continuous efforts of the Foundation’s Board of Directors and staff as well as our Medical and Scientific Advisors and the hundreds of Foundation volunteers.

50% Reduction in Diagnosis Time
The Foundation was excited to announce that we surpassed our 5 year breakthrough goal: To Shorten the time to diagnose Sjögren’s by 50% in 5 years and it now currently takes 2.8 years, down from 6 years, to receive a proper diagnosis.
Over $3 million raised
The Sjögren's Foundation raised over $3 million dollars to support our mission. These funds are being used to further research, education, patient initiatives and awareness of this complex disease.

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Faces of Sjögren’s

Patients share their journey with Sjögren's starting from their first thought after being diagnosed to where they are now.

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