The Sjögren’s Foundation Hosts a Congressional Briefing to Advocate for Sjögren’s, Lupus, and All Those Living with Autoimmune Diseases, and Acknowledges New House Resolution 245.
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The Rise of Autoimmune Diseases
Advocacy, General Information —
Read MoreA Lifetime of Advocacy Recognized: Sjögren’s Foundation Leader Kathy Hammitt Receives the 2025 Jack Hein Public Service Award
Advocacy, General Information —
Read More2024 in Review: Letter from Sjögren's Foundation CEO, Janet E. Church
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Read MoreFrom Diagnosis to Self-Advocacy, Robert's Story with Chronic Fatigue and Pain
Advocacy, General Information, Symptoms —
Read MoreListen to Your Gut! David's Experience with Fatigue and GI Symptoms
Advocacy, Diagnosis, General Information, Symptoms —
Read MoreMen Get Sjögren’s Too: Ray’s Experience with Peripheral Neuropathy
Advocacy, Diagnosis, General Information, Symptoms —
Read MoreLanguage Matters! The International Sjögren’s Community Changes Sjögren’s Syndrome to Sjögren’s Disease!
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