News

Ana Vieira’s journey with Sjögren’s disease spans decades of unanswered questions, delayed diagnosis, and determination. Today, as Co-founder and Vice President of Sjögren Europe, she draws on her experience to advocate for greater awareness, research, and care for people living with the disease. Read more που θα πηγαινει στο παρακάτω κείμενο

SpiderWeb: A new tool for people living with Sjögren Disease Sjögren Europe is pleased to introduce SpiderWeb, a digital tool designed to help people living with Sjögren Disease reflect on their symptoms and prepare for conversations with their healthcare professionals. Originally developed by the Dutch Sjögren patient community, SpiderWeb combines the Sjögren’s Symptoms Card with

We would like to inform our members and partners about an important update that has just been officially announced: The international consensus to change the name Sjögren’s syndrome to Sjögren’s disease has now been formally published in Nature Reviews Rheumatology (read the article here). This change represents a major step forward in how the condition