This week Andreas’ is running with the German Lupus association who are celebrating their 30th anniversary this year – and hosting our annual LUPUS EUROPE convention as part of those celebrations. Click the flag to see more.
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Lupus Europe is the umbrella association of currently 30 national lupus self-help organisations throughout Europe, and supports people with lupus in Europe.
✅ Check ⬇️ the recipients of the #Lupus Mechanisms and targets 🎯 Award 🏆 from @LupusResearch Alliance. These research projects will help us understand the complex pathogenesis 🔎 of #SLE and hopefully ✨ find new treatments. Proud to be part of the scientific advisory board 👍
🚨 Depression is very common in #lupus, we should check for it!
Among several disease, depressive episodes in #SLE showed a higher impact on the impairment of quality of life #qol ☹️
Check this small size #OpenAccess study published in @HC_TheJournal
Thank you all for your support on #RareDiseaseDay!
🤩 Thank you for your support this #RareDiseaseDay!
💪 Along with organisations like @rarediseaseday and @eurordis, we will carry on working towards an early diagnosis, access to treatment and equality for #RareDisease patients 🙌
👶 Neonatal #lupus is a rare congenital disorder that some infants of mothers with lupus and anti-Ro/SSA and/or anti-La/SSB antibodies develop.
🫀 The most serious complication of neonatal lupus is a heart condition known as congenital heart block
🦋 #Lupus is a #RareDisease that affects nearly 500,000 people in Europe and over 5 million people in the world.
‼️However, lupus affects not only patients but also their loved ones. Let's raise awareness of the importance of an early diagnosis
🚨 𝐋𝐚𝐬𝐭 𝐜𝐡𝐚𝐧𝐜𝐞 𝐭𝐨 𝐜𝐨𝐦𝐩𝐥𝐞𝐭𝐞 𝐭𝐡𝐞 𝐬𝐮𝐫𝐯𝐞𝐲❗
🚪 The #RarERNPath #SLE survey is closing today!
🦋 If you live with lupus in Europe, don't miss out on this opportunity to tell your story and help the European lupus community!
🚨 IT'S RARE DISEASE DAY GLOBALLY! 🚨 Join us marking #RareDiseaseDay 2024! Spread awareness, share stories, and support those living with rare diseases. Together, we make a lasting impact! #ShareYourColours
Welcome to Lupus Europe. To join our pan-European community, please contact us.