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🌟 Living with #Sjögren’s means living with uncertainty. The chronic fatigue, the dryness… but also the unknown. 🤝 Together, we raise awareness, amplify #patient voices, and work towards better recognition and care for this often misunderstood disease. #SjögrenAwarenessMonth

Sjögren Europe Webinar, D-1 📣 Don't forget to register for this very interesting webinar on physical activity in #Sjögren's disease 🌟 👉 lc.cx/4U0kO_ 💙 Join us on Tuesday, April 15 at 17.00 CET with Suzanne Boezerooij-Arends #Sjögrenawarenessmonth #Disease #RMDS

🌟 Sjögren Awareness Month 🌍 Sjögren’s isn’t just dryness — it’s chronic fatigue, pain, cognitive fog… and too often, disbelief. We work to make the invisible visible. Let’s choose empathy. 💙 #Sjögren #SjögrenAwarenessMonth #InvisibleIllness #ChronicPain

🌟 #SJÖGREN #AWARENESS #MONTH 🌍 Living with Sjögren’s #disease means facing a complex, invisible, and often misunderstood disease — it’s time to give it the visibility and recognition it truly deserves. Together we are stronger and let’s make your voice heard ! 📣

Because some pain can’t be seen. Because there are silent battles behind a smile. Because sometimes, the hardest part isn’t the pain itself… but having to prove it exists. 💙 To those fighting silently: your #pain is real. #Sjögrenawarenessmonth #Disease #Invisibleillness

Brain fog, slow thinking, forgetfulness, speech struggles — invisible yet daily challenges for those with Sjögren’s. 🌟 Kindness, patience, and understanding make a world of difference. 💙 #SjogrenEurope #BrainFog #InvisibleDisabilities #SjögrenAwarenessmonth

🌍 Sjögren’s Awareness Month ends — but our voice stays strong 💙 Thank you for sharing, supporting & raising awareness 🌟 You’ve shown one powerful truth: you are not alone. We keep going. Together. 💙 #SjögrenEurope #SjögrenAwareness #YouAreNotAlone #Sjögrendisease

⏰ Were you unable to attend the last #webinar on #physical #activity in #Sjögren's #disease? Watch the replay below, along with the full presentation by Suzanne Boezerooij-Arends PhD! 🎥 👉 lc.cx/05xfq_ Don't hesitate to ask questions in the comments ⬇️

Living with #Sjögrendisease ? 🌟 Our new guide offers simple daily tips to ease dryness, pain & fatigue. Small changes = big comfort. 💙 Check it out & share! #AutoimmuneDisease #ChronicIllness #SjögrenEurope #HealthTips #PatientSupport #Wellbeing

Meet Katy Antonopoulou, President of Sjögren Europe 💙 Though she doesn’t have Sjögren’s, she knows: 👉 Every patient is unique 👉 Living well is possible “Every patient deserves to be supported, understood & empowered.” #Sjögrendisease #ChronicIllness #PatientPower

🎥 Replay available ! Watch the ERN ReCONNET webinar - “Unmet Needs in Childhood-Onset Sjögren’s Disease”: With Dr Edoardo Marrani and our board member Ana Vieira 🌟 ▶️ youtu.be/rX2KSTrWh2Y #Sjögrendisease #ChildhoodSjögren #ERNReCONNET

Meet Ana, Vice President of #Sjögren Europe ⭐️. After more than 20 years of uncertainty, she was diagnosed with Sjögren’s at 49. Today, she shares her story of pain, resilience & hope to raise #awareness and support others. #AutoimmuneDisease

Welcome to Sjögren’s Australia! ✨🌏 Sjögren Europe proudly shares the launch of our Australian partner this Monday, June 2nd — a key step in global advocacy for Sjögren’s. Visit, follow & share their pages. Together we are stronger ! 💙 #SjögrenAustralia #SjögrenDisease

📢 Sjögren Europe will be at EULAR in Barcelona 🇪🇸! 📍 Meet our board members at Glass Walkway / O11 📅 From June 11 to 14, 2025 Let’s connect and advance research on Sjögren’s disease 💙 🔗 More info: eular.org #SjogrenEurope #EULAR2025

Breaking news 📣 The scientific publication confirming the name change of Sjögren’s disease is out : lc.cx/h1vz5U At EULAR today, Coralie Bouillot and Katherine Hammitt present how patients were involved in the renaming process. #Sjögrendisease #Sjögrenfoundation

✨ Massive bravo to Prof. Nocturne for her brilliant presentation and thank you for the kind words towards patient community !

🔍 Fatigue is a major burden. A recent study shows fatigue severely affects daily functioning and emotional health for many living with #Sjögren’s. Have you experienced this? Comment below or tag someone who understands ⬇️ #SjögrenFatigue #ResearchMatters #Disease #Unmetneeds

« Everything You Always Wanted to Know About Clinical Trials (But Were Afraid to Ask) » Open and honest discussion with clinicians involved in research, patients and representatives from pharma. 🔗 Register now: lc.cx/oXeZkg #WSD2025 #SjögrenDisease #Unmetneeds

🎥 “It’s not just dry eyes or mouth…” “It’s exhaustion, pain, and not being believed.” – A real patient voice. 📣 Share this to help others understand what life with Sjögren’s truly looks like. #LifeWithSjögren #PatientVoices #SjögrenDisease #Unmetneeds