World Sjögren’s Day
Join us in recognizing Sjögren's syndrome, an often overlooked autoimmune disorder.
- Roots
- Founded by the Sjögren's Foundation; observed on the birthday of Dr. Henrik Sjögren
- Vibe
- Community-driven and supportive
- Also on Jul 23
- Gorgeous Grandma Day · Lemon Day · Refreshment Day
- Hashtag
- #WorldSjgren8217sDay
3 ways to celebrate
Read a patient story
Find a firsthand account and learn what living with it looks like.
Raise awareness together
Chat with friends about the condition and share a resource link.
Organize a small drive
Collect donations for a support group in your building or class.
Fast facts
The story
Sjögren's syndrome is an autoimmune disorder that primarily affects moisture-producing glands, leading to dry mouth and dry eyes. It can also impact other organs, making it a complex condition that often goes undiagnosed. The day aims to shed light on this condition that affects 4 million Americans, disproportionately impacting women. By raising awareness, we can foster understanding and support for those living with this condition.
Read the full story
World Sjögren's Day was established by the Sjögren's Foundation, an organization dedicated to improving the lives of individuals diagnosed with the syndrome. Events and educational programs are held globally, from the United States to Europe, providing resources and community support. This day encourages patients, families, and healthcare professionals to unite for a common cause, creating a network of awareness and advocacy.
The observance of this day is more than just a date on the calendar; it represents a significant push for research funding and improved patient care. With the right support, individuals with Sjögren's can lead fulfilling lives, despite the challenges posed by the disease. As awareness grows, so does the hope for better treatments and potential cures.
As we recognize World Sjögren's Day, it is crucial to remember the individual stories behind the statistics. Many people live with daily challenges, and by sharing these experiences, we can foster empathy and understanding. Together, we can build a community that champions health equity and supports those affected by Sjögren's syndrome.
Did you know?
Women Predominance
90% of Sjögren's patients are women.
Global Awareness
Awareness events take place in countries around the world.
Historical Roots
First described by Dr. Henrik Sjögren in 1933.
Overlap with Other Conditions
Often associated with rheumatoid arthritis.
Symptoms Variability
Symptoms can vary widely among individuals.
Ongoing Research
Research is crucial for finding better treatments.
Community Engagement
Local events boost engagement and support.
Around the world
Every culture celebrates a little differently.
- USUnited StatesHome to many awareness initiatives.
- CACanadaSupports Sjögren's research funding.
- GBUnited KingdomHosts events for awareness.
- AUAustraliaEngages in community education.
- DEGermanyPromotes research and support.
- FRFranceParticipates in global awareness efforts.
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