world-sjogrens-day-july-23

World Sjogrens Day July 23

In the tapestry of medical history, few stories are as fascinating as the discovery and understanding of Sjogren's Syndrome, a condition that turned the spotlight on how our bodies can sometimes turn against themselves. Imagine being the first to connect the dots between seemingly unrelated symptoms like dry eyes and dry mouth, and realizing it's part of a larger, more complex puzzle. That's exactly what Henrik Sjogren, a Swedish ophthalmologist, did in 1933, setting the stage for a journey of discovery that would span decades. His groundbreaking work not only shed light on this perplexing condition but also paved the way for the establishment of World Sjogren's Day in 2012, a day dedicated to raising awareness and supporting those battling this syndrome. From the initial curiosity of one man to a global movement, the story of Sjogren's Syndrome is a testament to the power of medical research and the enduring spirit of the human community in facing health challenges.

Key Takeaway

Sjogren’s Syndrome is an autoimmune disorder that affects the moisture-producing glands, first described by Henrik Sjogren in 1933.
World Sjogren’s Day was established in 2012 to raise awareness and support for those affected by the condition, honoring Henrik Sjogren’s pioneering work.

Timeline

1933
Discovery of Sjogren’s Syndrome
Swedish ophthalmologist Henrik Sjogren first describes the condition that would later bear his name, identifying the triad of dry eyes, dry mouth, and rheumatoid arthritis.
1959
First International Symposium on Sjogren’s Syndrome
The first international symposium on Sjogren’s syndrome is held in New York City, bringing together experts from around the world to discuss the latest research and treatment options for the disease.
1971
Formation of the Sjogren’s Syndrome Foundation
The Sjogren’s Syndrome Foundation is established in the United States to promote research, education, and awareness of Sjogren’s syndrome.
1985
Recognition of Sjogren’s Syndrome as a Systemic Disease
The American College of Rheumatology recognizes Sjogren’s syndrome as a systemic disease, rather than simply a complication of other autoimmune disorders.
2002
Development of the European League Against Rheumatism (EULAR) Sjogren’s Syndrome Disease Activity Index
The European League Against Rheumatism develops a standardized tool for measuring disease activity in patients with Sjogren’s syndrome.
2012
Establishment of World Sjogren’s Day
July 23 is established as World Sjogren’s Day to raise awareness of the disease and promote education and research.
2016
Launch of the Sjogren’s Syndrome Awareness Month
The Sjogren’s Syndrome Foundation launches the Sjogren’s Syndrome Awareness Month campaign, which takes place every April to raise awareness and support for people living with the disease.

Day Activities

  1. Educational Workshops: On World Sjogren's Day, experts host enlightening workshops aimed at demystifying this autoimmune disorder for the general public. Attendees learn about the latest research, treatment options, and ways to manage symptoms. These sessions often feature interactive Q&As, making sure everyone leaves with their curiosities satisfied and misconceptions cleared up.

  2. Social Media Blitz: Leveraging the power of hashtags and shares, advocates and organizations go all out on platforms like Twitter, Facebook, and Instagram. They share stories, infographics, and videos that highlight the struggles and triumphs of those living with Sjogren's Syndrome. This digital rally not only spreads awareness far and wide but also fosters a sense of community among those affected.

  3. Fundraising Fun: From charity runs to bake sales, supporters put on their creative hats to raise funds for Sjogren's research and patient support services. Every penny collected goes towards making a difference in the lives of those battling this condition. These events are not just about raising funds; they're also about bringing people together for a cause close to their hearts.

Interesting Facts

1. Henrik Sjogren's Pioneering Discovery

In 1933, Henrik Sjogren first described dry eyes and mouth symptoms, identifying Sjogren's Syndrome.

2. Diagnostic Criteria Established

By 1982, specific diagnostic criteria for Sjogren's Syndrome were set, enhancing diagnosis and treatment.

3. World Sjogren's Day Inception

World Sjogren's Day started on July 23, 2012, to honor Henrik Sjogren and raise syndrome awareness.

4. Annual Global Awareness

Since its inception, World Sjogren's Day has sparked global activities to support affected individuals annually.

5. Ongoing Medical Research

Research on Sjogren's Syndrome reflects continuous efforts to understand and treat autoimmune disorders effectively.

Why We Love This Day

  • Celebrating Henrik Sjogren's groundbreaking work: We love this day because it honors Henrik Sjogren, who first shone a light on Sjogren's Syndrome. His dedication to understanding this complex autoimmune disorder has paved the way for advancements in diagnosis and treatment, making life better for countless individuals.

  • Raising awareness and support: Another reason to cherish July 23 is its role in boosting awareness about Sjogren's Syndrome. This day brings people together, spreading knowledge and fostering a supportive community for those navigating the challenges of living with this condition. It's all about lending a hand and showing we care.

  • Fostering medical advancements: Lastly, World Sjogren's Day is a beacon of hope for future breakthroughs. It not only commemorates past achievements but also inspires ongoing research and development. Every year, this day reminds us of the progress made and the journey ahead in the fight against autoimmune disorders.

Past & Future Dates

Month Day Year
JULY 23 2022
JULY 23 2023
JULY 23 2024
JULY 23 2025
JULY 23 2026
JULY 23 2027
JULY 23 2028

FAQ

What is World Sjögren's Day?

World Sjögren's Day falls on July 23, dedicating a spotlight to the autoimmune disorder known as Sjögren's Syndrome. It's a day when awareness spreads far and wide, shining a light on the symptoms and challenges faced by those with the syndrome, all in the hopes of fostering understanding and support.

When is Sjögren's Day in 2024?

Mark your calendars for July 23, 2024, for the next World Sjögren's Day. This day provides a golden opportunity for individuals touched by Sjögren's syndrome to elevate awareness and share knowledge with their personal circles, including family, friends, and co-workers.

What is it like living with Sjögren's syndrome?

Living with Sjögren's syndrome often means facing daily challenges such as dry eyes, a dry mouth, enduring fatigue, and joint pain. Though these are the signature symptoms, Sjögren's is far-reaching, impacting the entire body and making fatigue one of the condition's most taxing elements.

When is the Sjögren's Awareness Month?

April is recognized as Sjögren's Awareness Month. It's a time when the spotlight turns to one of the most prevalent yet under-recognized autoimmune diseases. With an estimated 4 million Americans living with Sjögren's, the majority being women, this month is crucial for amplifying voices and spreading knowledge.