International Day July 23

World Sjögren’s Day

Why it matters

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WELCOME TO AWARENESS

Join us in recognizing Sjögren’s syndrome—an often overlooked autoimmune disorder.

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━━━━ FAST FACTS ━━━━
WHEN
July 23
ORIGIN
Established in 2010 by Sjögren's organizations worldwide
STAT
Approximately 4 million Americans are affected
STAT
90% of those affected are women
VIBE
Community-driven and supportive
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THE STORY

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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.

World Sjögren’s Day was established in 2010, driven by organizations 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.

Awareness is the first step towards change.

— UNKNOWN
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WORTH KNOWING

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#1
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Understanding Sjögren's

Learn about symptoms and effects.

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Educational Resources

Access materials for better knowledge.

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Community Support

Find local and online support groups.

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Advocacy Matters

Get involved in awareness campaigns.

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AROUND THE WORLD

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🇺🇸 United States

United States

Home to many awareness initiatives.

🇨🇦 Canada

Canada

Supports Sjögren’s research funding.

🇬🇧 United Kingdom

United Kingdom

Hosts events for awareness.

🇦🇺 Australia

Australia

Engages in community education.

🇩🇪 Germany

Germany

Promotes research and support.

🇫🇷 France

France

Participates in global awareness efforts.

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DID YOU KNOW?!

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TRIVIA

Women Predominance
90% of Sjögren’s patients are women.

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Global Awareness
Observed in over 50 countries.

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Historical Roots
First described by Dr. Henrik Sjögren in 1933.

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Overlap with Other Conditions
Often associated with rheumatoid arthritis.

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Symptoms Variability
Symptoms can vary widely among individuals.

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Ongoing Research
Research is crucial for finding better treatments.

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Community Engagement
Local events boost engagement and support.

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READ MORE

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HEALTH & WELLNESS

The Sjögren's Syndrome Handbook

By Dr. T. A. Brown

A comprehensive guide for understanding and managing Sjögren’s.

PERSONAL STORIES

Living with Sjögren's

Edited by J. Smith

Personal accounts from those affected by the syndrome.

MEDICAL REFERENCE

Autoimmunity: A Comprehensive Guide

By Dr. M. Johnson

Explores various autoimmune diseases including Sjögren’s.

COMMUNITY SUPPORT

Finding Your Tribe

By R. A. Lee

A guide to finding support groups and networks.

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PAIR IT WITH

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HYDRATION MATTERS

Stay hydrated to ease symptoms.

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EDUCATE YOURSELF

Knowledge reduces stigma.

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SUPPORT EACH OTHER

Community is vital for coping.

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RAISE AWARENESS

Every voice counts.

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Spread the Word

Join us in raising awareness for Sjögren’s syndrome this July 23. Share information and support those affected.

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