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#Lupus100
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🦋 Turn to your association for support.

🇪🇺 There are many orgs across Europe that can help you & your child cope with #lupus.

Look for the one closest to you: www.lupus-europe.org/lupus-members/

More, at #Lupus100 & #LupusGPT lupus100.org/en/questions... lupusgpt.org

#WORDDAY2026

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🍏 A well-balanced diet, with plenty of fruits, vegetables and whole grains, is key for #lupus patients.

🦋 The only specific diet that has been proven to improve #lupus activity and symptoms is the Mediterranean diet.

More ℹ️ on #Lupus100 https://f.mtr.cool/lpwwrvswqq

#WORDDAY2026

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💊Apart from pharmacological treatment, other non-pharmacological measures can help in #lupus management.

🏃Did you know exercise has been shown to improve SLE symptoms like #fatigue?

More at #Lupus100 https://f.mtr.cool/jyyuwigvne

Also, follow our exercise programme!

#WORDDAY2026

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#Lupus might sound scary at first, but the diagnosis doesn't mean your child will not be able to have a normal life.

Talk to your doctor about infection prevention & self-care measures.

Find reliable information on #Lupus100 https://f.mtr.cool/zrbceqdwgg in your language
#WORDDAY2026

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🛠️ Maintenance alert:

We are carrying out maintenance work on our main website.

🌐 During this time, you may experience limited access or temporary disruptions.

In the meantime, you can visit #LupusGPT and #Lupus100 for lupus info!

Thank you for your support & understanding!

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🛠️ Maintenance alert:

We are carrying out maintenance work on our main website.

🌐 During this time, you may experience limited access or temporary disruptions.

In the meantime, you can visit #LupusGPT and #Lupus100 for lupus info!

Thank you for your support & understanding!

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🦋 We can say it louder, we can say it clearer… &, with #Lupus100, also in 19 languages!

❌ Lupus is NOT contagious.

✨ Help break the myth:

-Share a post on social media
-Use lupus100.org to find the explanation in your language and share -links in this thread! ⤵️

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🦋Kudos to our Vice-Chair & Secretary, Annemarie Sluijmers, who joined the #GlobalSkin-Europe Health Policy Influencers Forum to share the impact of #LupusGPT & #Lupus100 in improving validated #lupus info for better care.

Thank you, GlobalSkin, for ensuring the lupus patient voice is heard!

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🚨 Misconceptions can appear anywhere.

🤝 Turning to patient orgs & resources like #Lupus100 & #LupusGPT helps avoid misconceptions that can cause harm & ⬇️ QoL of people with lupus.

Share this post & encourage others to visit https://lupus100.org/ & https://lupusgpt.org/

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📅Save the date!

@eurordis.bsky.social Patient Partnership Webinar – The #Lupus100 Project
🗓️18 Sept | 18:00 CET

With Prof Eric Hachulla, our Chair Jeanette Andersen, our General Secretary Zoe Karakikla-Mitsakou, & Alain Cornet (our Organisation Coach).

Register now! us02web.zoom.us/meeting/regi...

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🌟Unlike other AI tools, #LupusGPT will 𝗻𝗼𝘁 make up answers. It will let you know if the information is unavailable in its database.

✅Every response is based on a rigorously curated repository of scientific documents, including @eular_org recommendations & #Lupus100 website

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💡 #Lupus100, developed by ERN ReCONNET & Lupus Europe, is a multilingual free lupus resource.

Do you want to know more? Register for this EURORDIS webinar with Prof E Hachulla; our Chair, Jeanette Andersen & Zoe Karakikla-Mitsakou, our General Secretary.

www.eurordis.org/improving-pa...

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🛠️Scheduled maintenance alert

Today, between 12:00 and 18:00 CET, we will be carrying out maintenance work on both our main website & #Lupus100 website.

🌐 During this time, you may experience limited access or temporary disruptions.

Thank you for your support & understanding!

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👏Excellent session by our Chair, Jeanette Andersen, on #LupusGPT & #Lupus100: multilingual AI-powered tools offering free, validated & accessible info.

Want to learn more or replicate it in other diseases? Visit us at Booth O15- NPO area, glass walkway, near Hall 8.1!

#EULAR2025

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🦋 While #Lupus100 is a very powerful tool, it is static.

🌈 That’s why we, at Lupus Europe, have created #LupusGPT: a multilingual, dynamic AI tool built on specific, validated resources to ensure patients receive high-quality information.

lupusgpt.org

#EULAR2025

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🔔Don’t miss this session that our Chair, Jeanette Andersen, will deliver today at @eular.org Congress!

🎤“Developing new AI resources: #Lupus100 & #LupusGPT
🕝14:30- Room C3

💡Discover how patient-led innovation can shape #lupus education

https://lupusgpt.org/
https://lupus100.org/

#EULAR2025

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It is estimated that about 50% of #SLE patients will suffer from #lupus nephritis, one of SLE's 🔝dangerous & frequent complications.

Routine checkups➕available treatments make it possible for 60–70% of patients to achieve complete or partial remission

#WorldLupusDay
#Lupus100

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#Lupus is an autoimmune disease that affects nearly 500,000 people in Europe and over 5 million people in the world.

It affects not only patients but also their loved ones.

Let's raise awareness of the importance of an early diagnosis
#WorldLupusDay
#MakeLupusVisible
#Lupus100

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🚨 #Lupus is a complex and heterogeneous systemic autoimmune disease in which the body's immune system attacks your own tissues and organs, causing inflammation and damage in any part of the body

Visit #Lupus100 & #LupusGPT for more!

#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 https://lupus100.org & https://lupusgpt.org & find reliable information about #lupus in many languages!

#MakeLupusVisible

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🦋 How much do you really know about lupus?

Try #SLAKE — a quick, easy tool (available in 20 languages) to assess your #lupus knowledge!

👉 Take it now + keep learning at #Lupus100 & #LupusGPT!

https://maladie-autoimmune.fr/SLAKE/

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🦋 Turn to your #lupus association for support.

🇪🇺 There are many organisations across Europe that can help you and your child cope with the disease.

👀 Look for the one closest to you here ➡️ https://f.mtr.cool/crflcqlovr

ℹ️ More, at #Lupus100 https://f.mtr.cool/wswnsdvtdu

#WORDDAY2025

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🍏 A well-balanced diet, with plenty of fruits, vegetables and whole grains, is key for #lupus patients.

🦋 The only specific diet that has been proven to improve #lupus activity and symptoms is the Mediterranean diet.

More ℹ️ on #Lupus100 https://f.mtr.cool/upjssjygws

#WORDDAY2025

1 0 0 0
Post image

💊Apart from pharmacological treatment, other non-pharmacological measures can help in #lupus management.

🏃Did you know exercise has been shown to improve SLE symptoms like #fatigue?

More at #Lupus100 https://f.mtr.cool/zthpwqrolr

Also, follow our exercise programme!

#WORDDAY2025

0 0 0 0
Post image

#Lupus might sound scary at first, but the diagnosis doesn't mean your child will not be able to have a normal life.

Talk to your doctor about infection prevention & self-care measures.

Find reliable information on #Lupus100 https://f.mtr.cool/jwfrgklhmj in your language
#WORDDAY2025

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#LupusGPT has been developed by Lupus Europe & validated by leading lupus experts & patients.

This AI tool ensures 100% reliability by exclusively using information meticulously verified and sourced from top-tier scientific publications and #Lupus100.

https://lupusgpt.org/

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⁉️ Do you want to know more about diet & #lupus?

✅ Check out the #Lupus100 website, where you can find reliable information about lupus in a patient-friendly language.

🔊 Available in multiple European languages! ⤵️

lupus100.org/en/questions/should-we-f...

🇩🇰 ht…

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