World Sjogren’s Day
Why it matters
RAISE AWARENESS
On July 23, we unite to bring attention to Sjogren’s syndrome and support those affected.
THE STORY
World Sjogren’s Day takes place annually on July 23, shining a light on Sjogren’s syndrome, a chronic autoimmune disorder characterized by dry eyes and mouth, among other symptoms. This day was established in 2012 by the Sjogren’s Foundation to promote awareness and education around the condition, which affects millions of individuals worldwide—predominantly women. By sharing stories and resources, the day encourages a greater understanding of the disease and its impact on daily life.
Sjogren’s syndrome can manifest in various ways, including fatigue, joint pain, and complications in organs like the kidneys and liver. Despite its prevalence, many people remain unaware of this condition, often leading to misdiagnosis or delayed treatment. World Sjogren’s Day aims to change that narrative by providing a platform for education and advocacy. Medical professionals and patients alike are encouraged to join the conversation and share their experiences, fostering a sense of community and support.
Around the globe, communities are coming together to recognize this important day. Events may include informational seminars, social media campaigns, and support group meetings. These gatherings not only raise awareness but also provide a space for individuals affected by Sjogren’s syndrome to connect and share resources. By highlighting the challenges and triumphs faced by those living with this illness, we can cultivate a more compassionate society that acknowledges and supports chronic illness.
In the spirit of World Sjogren’s Day, individuals are encouraged to take action—whether through education, fundraising, or simply sharing their stories online. With continued awareness and support, we can help those impacted by Sjogren’s syndrome feel less isolated and more understood. Join us in advocating for a future where autoimmune disorders are recognized and addressed with the urgency they deserve.
Awareness is the first step towards understanding.
WORTH KNOWING
Dryness Awareness
Understand the symptoms related to dry eyes and mouth.
Community Support
Join support groups to connect with others.
Educational Resources
Access materials to learn more about Sjogren’s.
Donate
Contribute to research and support organizations.
AROUND THE WORLD
DID YOU KNOW?!
Historical Insight
Sjogren’s syndrome was first described in 1933.
Famous Faces
Some celebrities have openly discussed their diagnosis.
Misdiagnosis
It often takes years for accurate diagnosis.
Global Impact
Sjogren’s affects people worldwide, transcending borders.
Research Funding
Funding for Sjogren’s research is critical for advancements.
Community Strength
Support networks provide emotional and informational help.
Ongoing Advocacy
Advocacy efforts continue to grow each year.
READ MORE
The Sjogren's Book
By Dr. Daniel J. Wallace
A comprehensive guide to understanding Sjogren’s syndrome.
Living with Sjogren's
By Mary Ellen Ashford
Personal accounts of living with this chronic condition.
Sjogren's Syndrome: The Facts
By Dr. Zhiwei Zhang
An informative resource on the syndrome’s effects.
Coping with Sjogren's
By Nancy L. Cummings
Strategies for managing symptoms and improving quality of life.
PAIR IT WITH
Don’t forget to celebrate on July 23.
Share facts and stories with friends.
Collaborate with local organizations.
Host discussions about autoimmune conditions.
Spread Awareness Now
Join us in recognizing World Sjogren’s Day by sharing information and supporting those affected by this autoimmune disorder.