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💜 World Lupus Day 🌍
At #ERNReCONNET, we are profoundly committed to supporting the lupus community @LupusEurope
Together, let’s #MakeLupusVisible by raising awareness and sharing knowledge
🦋 𝐓𝐨𝐝𝐚𝐲 𝐢𝐬 #𝐖𝐨𝐫𝐥𝐝𝐋𝐮𝐩𝐮𝐬𝐃𝐚𝐲❗
And now it is easier than ever to raise #LupusAwareness thanks to #Lupus100 and #LupusGPT!
Check https://lupus100.org/ & https://lupusgpt.org & find reliable information about #lupus in many languages!
#MakeLupusVisible
✅ Today, 10th of May 2026, is the world #lupus day 🦋
Re-tweet 🔄, spread the word, let the world 🌍🌎🌏 be aware of this complex #autoimmune disease with so many facets 💎, including invisible ones.
#worldlupusday
#lupusday
🤩 May 10 is #WorldLupusDay! And our Youth Group is commemorating it with a webinar on fertility & family planning in young people with lupus.
📅 May 10
🕖 7 pm CET
🎙️ Prof. @lauraandreoli80
🗣️Moderated by our Chair, @Jeanette_Lupus
Join us! Email secretariat@lupus-europe.org
Joining the global community
raise #Lupus awareness with @LupusEurope
Together we can #MakeItCount on May 10. #LupusAwarenessMonth
🌈 Beyond what you’ve experienced, something awaits.
🌟 A new way to approach your consultation is coming.
Make your consultation count.
💥 Stay tuned
#MakeItCount
🆘 Skin matters in lupus.
‼️75–80% of people with SLE experience skin involvement, yet skin lupus has seen no new treatment options for over 80 years.
WHO’s draft Global Action Plan on Skin Diseases is open for consultation.
🗣️ Add your voice by 10 May 👇

#WHO has opened a public consultation on its draft Global Action Plan for Skin Diseases.
Your input can help shape how countries act and ensure accountability for the 2B+ people affected.
🗣️ Make your voice heard
📅 Deadline: May 10, 2026
👉 https://www.who.int/news-room/articles-detail/public-consultation--draft-global-action-plan-on-skin-diseases-as-a-global-health-priority-(gap-skin)
❤️🔥 Something big is coming...
... this #WorldLupusDay 🌍.
#MakeItCount
🚨 #Lupus is a complex and heterogeneous systemic autoimmune disease in which the body's immune system attacks its own tissues and organs, causing inflammation and damage in any part of the body
Visit #Lupus100 & #LupusGPT for more!
lupus100.org/
lupusgpt.org/
#MakeItCount
#WorldLupusDay
#MakeLupusVisible
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🦋 𝐓𝐨𝐝𝐚𝐲 𝐢𝐬 #𝐖𝐨𝐫𝐥𝐝𝐋𝐮𝐩𝐮𝐬𝐃𝐚𝐲❗
And now it is easier than ever to raise #LupusAwareness thanks to #Lupus100 and #LupusGPT!
Check lupus100.org/ & lupusgpt.org & find reliable information about #lupus in many languages!
#MakeItCount
#MakeLupusVisible
... See MoreSee Less
0 CommentsComment on Facebook
🤩 May 10 is the #WorldLupusDay! And our Youth Group is commemorating it with a 𝐬𝐩𝐞𝐜𝐢𝐚𝐥 𝐰𝐞𝐛𝐢𝐧𝐚𝐫 focused on one of the most important and often overlooked topics for young people living with lupus: 𝐟𝐞𝐫𝐭𝐢𝐥𝐢𝐭𝐲 𝐚𝐧𝐝 𝐟𝐚𝐦𝐢𝐥𝐲 𝐩𝐥𝐚𝐧𝐧𝐢𝐧𝐠.
👩⚕️ How does lupus affect fertility?
💊 What should you consider before planning a pregnancy?
🧠 How can healthcare professionals better support young patients in these decisions?
This session brings together clinical expertise and real patient perspectives to provide clear, practical insights.
📅 𝐌𝐚𝐲 𝟏𝟎
⏰ 7 pm CET (i. e. Paris time)
🎙️ Speaker: Prof. Laura Andreoli
🗣️ Moderated by our Chair, Jeanette Andersen
👥 Organised with the Lupus Europe Youth Group
📌 Whether you are living with lupus, supporting someone who is, or working in healthcare, this webinar is for you.
👉 Don't wait any longer and register now! Send an email to secretariat@lupus-europe.org
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🌈 Beyond what you’ve experienced, something awaits.
🌟 A new way to approach your consultation is coming.
Make your consultation count.
💥 Stay tuned
#MakeItCount
... See MoreSee Less
0 CommentsComment on Facebook
Welcome to Lupus Europe. To join our pan-European community, please contact us.

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