Your input as a patient group is needed in a study seeking patient group perspectives on Bio-similars. To participate please click here.
Your input as a patient group is needed in a study seeking patient group perspectives on Bio-similars. To participate please click here.
🔊Hot off the press!
💜Treatment adherence is important, complex and multifactorial.
An interesting viewpoint on putting @eular_org recommendations into practice, with Chair of Lupus Europe’s Board @Jeanette_Lupus, @SaraTalarico2, @MartaMartamosca et al
https://doi.org/10.1016/j.ero.2026.100261
Ask. Listen. Learn. Thank you @LupusEurope
Life with chronic pain is not fun.
#WorldDayAgainstPain
🔴 Pain is an invisible part of daily life for many people with #lupus.
📊 Our Swiss Knife Survey found that:
🔹 72.8% reported joint pain/swelling
🔹 62.6% reported muscle pain/weakness
On #WorldDayAgainstPain, let's make pain visible.
https://doi.org/10.1016/j.autrev.2025.103838
🔴Calling HCPs & patients!
This webinar is for you.
How can PROs bring the patient perspective into lupus consultations & potentially support better adherence & outcomes?
Join @LupusAcademy, @Jeanette_Lupus, Prof M Dall’Era & Prof R van Vollenhoven.
🔗 https://us06web.zoom.us/webinar/register/WN_pPQAXvBjSEqt0kyW5KCE7w#/registration
🔴 Arthritis is the swelling & tenderness of one or more joints.
It’s an illness that comprises many conditions that affect the joints, tissues around the joint, & other connective tissues: #lupus, rheumatoid arthritis & osteoarthritis, to name a few
#WorldArthritisDay #WAD2026
🚨Today is #WorldMentalHealthDay.
☝️Do you know that #lupus patients are at high risk of anxiety and #depression?
Always talk to your physician about how you feel. Addressing mental health problems promptly is key.
🦋 Know more. Visit #LupusGPT
https://lupusgpt.org/
Thanks, @felupus, for sharing our resources!
💜 Supporting and empowering our member organisations is at the heart of what we do at Lupus Europe.
It was great to have you join us in Barcelona for the #LupusConvention!
#LupusConvention @LupusEurope
Presentan las Tarjetas de Consulta para Lupus, disponibles en 20 idiomas y en versiones femenina y masculina, para ayudar a las personas a prepararse para las consultas.
Tarjeta ➡️ 🔗https://lupus-europe.org/lupus-consultation-cards/
⬆️ Descárgate en tu idioma 😉⬆️
💃 That’s a wrap on the 2026 Lupus Europe Convention!
🦋 Three days of learning, sharing, practical ideas and plenty of laughter. Thank you to everyone who made Barcelona so special.
🇷🇸 Next stop: Belgrade for the 2027 #LupusConvention!
Welcome to Lupus Europe. To join our pan-European community, please contact us.

Info Center: https://lupus-europe.org/me-lupus/lupus-europe-info-center/
Survey Center: https://lupus-europe.org/me-lupus/lupus-europe-survey-center/
Blog: https://lupus-europe.org/blog/
Videos: https://lupus-europe.org/videos-on-demand/
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Twitter: https://twitter.com/LupusEurope