Mary Chapman, features writer —

To help shed light on what it’s like to live with Sjögren’s syndrome, a systemic autoimmune condition thought to affect about 4 million U.S. residents, this year’s Sjogren’s Awareness Month will focus on stories from the patients themselves. The annual April event is designed to showcase the disorder and…

A Regenstrief Institute research scientist will use a five-year, $4.7 million federal grant on a Sjögren’s syndrome biomarker research project and dental training program aimed at fostering collaboration among healthcare professionals and incorporating into clinical practice research on disorders that affect oral health. Specifically, the grant from the National…

Supporters around the world are preparing to use their voice to educate others about Sjögren’s syndrome for World Sjögren’s Day — set aside each July 23 to call attention to the chronic autoimmune disease. Sjögren’s syndrome is believed to occur in about 0.1% to 1% of the general…

To help people understand what life is like with Sjögren’s syndrome, a disorder that affects an estimated four million people in the U.S., this year’s Sjögren’s Awareness Month will again spotlight personal stories from patients. The event, observed each April, seeks to bring attention to the systemic autoimmune disease…

From sharing personal stories and educating others, to raising funds for research, supporters globally are poised to mark World Sjögren’s Day — set aside each July 23 to heighten awareness of the chronic autoimmune disorder. Sjögren’s syndrome is thought to occur in approximately 0.1% to 4% of the general…

This year’s Sjögren’s Awareness Month will focus on patient experiences to share glimpses into the lives of people with Sjögren’s syndrome, a complex disorder that is thought to affect four million U.S. residents. Each day in April, the Sjögren’s Foundation will showcase a different patient on its website and…

After a four-year effort led by the Sjögren’s Foundation, new health statistics codes in the U.S. — known as ICD-10 codes — recognizing Sjögren’s syndrome as a distinctive condition from “sicca” are now in effect. The codes are officially known as the International Statistical Classification of Diseases and…

To combat the continued spread of COVID-19 and its Delta variant, Sjögren’s syndrome patients should get a third dose of the Pfizer or Moderna vaccine, the Sjögren’s Foundation has recommended, pursuant to Centers for Disease Control and Prevention (CDC) guidelines. The CDC — the United States’ public…

From sharing inspirational stories to educating others, supporters are poised to mark World Sjögren’s Day, observed annually on July 23 to raise awareness about the disease. Awareness and education are crucial to increasing the recognition, diagnosis, understanding, and management of Sjögren’s syndrome, a chronic autoimmune disorder that predominantly affects…

Applications for a next round of Sjögren’s Foundation research grants are being accepted from U.S. investigators working to better understand Sjögren’s syndrome, a chronic immune system disorder, and improve patients’ lives. The one-year grants are available to basic and clinical scientists who hold an advanced degree at a U.S.