
Sjögren’s disease affects everyone differently. These are the stories of 5 people and how they found the connection between their seemingly unrelated symptoms.
Rachael’s story
Some Sjögren’s disease symptoms can seem invisible. For Rachael, they feel like something she’s been fighting most of her life. Hear how seeing a rheumatologist helped her finally connect the dots.
Daniel’s story
Daniel’s children call Sjögren’s disease his “forever sickness.” But he’s found ways to manage his symptoms—like carrying a go-bag with medications. Learn how sharing the fuller picture of what he was going through helped Daniel get to where he is today.
Susan’s story
Susan was traveling the world before she began questioning what was causing her fatigue. See how her 20-year journey and one Facebook post helped her connect the dots to Sjögren’s disease.
Paula’s story
When Paula was first diagnosed with Sjögren’s disease at a young age, she felt very alone and disconnected. Now she leads a support group for others diagnosed at a younger age. Watch Paula’s story about her journey from patient to advocate.
Megan’s story
Balancing work, family, and other responsibilities can be hard. It’s even harder when you’re also managing many different, unpredictable symptoms. Learn how finding the right doctor helped Megan see the fuller picture of Sjögren’s disease.
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