Lupus consultation cards-
A practical tool for patients and clinicians

These consultation cards are a simple practical tool designed by patients and lupologists to help you prepare for your appointment with your lupus specialist. They help you reflect in advance on the symptoms affecting you most, write down what you most want to raise, and prepare your top questions for the doctors.
The cards are free to use. Just download your language version below, fill it in before your appointment, either digitally on your phone or device or by printing it and completing it by hand, and take it with you to your appointment.

German Consultation Card

English Consultation Card

Portuguese Consultation Card

Bulgarian Consultation Card

French Consultation Card

Czech Consultation Card

Flemish Consultation Card

Greek Consultation Card

Icelandic Consultation Card

Italian Consultation Card

Lithuanian Consultation Card

Norwegian Consultation Card

Polish Consultation Card

Russian Consultation Card

Serbian Consultation Card

Spanish Consultation Card

Swedish Consultation Card

Estonian Consultation Card

German Consultation Card

English Consultation Card

Portuguese Consultation Card

Bulgarian Consultation Card

French Consultation Card

Czech Consultation Card

Flemish Consultation Card

Greek Consultation Card

Icelandic Consultation Card

Italian Consultation Card

Lithuanian Consultation Card

Norwegian Consultation Card

Polish Consultation Card

Russian Consultation Card

Serbian Consultation Card

Spanish Consultation Card

Swedish Consultation Card

Estonian Consultation Card

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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
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🆘 𝗦𝗸𝗶𝗻 𝗺𝗮𝘁𝘁𝗲𝗿𝘀 𝗶𝗻 𝗹𝘂𝗽𝘂𝘀.

🌍 The World Health Organisation has opened a public consultation on the draft Global Action Plan on Skin Diseases, a strategic framework that will guide governments in developing national plans on skin diseases.

🟣 Why is this important for the #lupus community?

👉 75–80% of people with SLE experience skin involvement. Skin lupus, including ACLE, SCLE and CDLE, has seen no new treatment options for over 80 years.

💬 This is an important opportunity to make sure that the voices of people living with lupus and the wider civil society community are heard.

📅 Deadline: 10 May- #WorldLupusDay
🔗 Add your voice and share with your community: www.who.int/news-room/articles-detail/public-consultation--draft-global-action-plan-on-skin-disea...
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🆘 𝗦𝗸𝗶�

❤️‍🔥 Something big is coming...

... this #WorldLupusDay 🌍.

#makeitcount
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📣 Register now by sending an email to secretariat@lupus-europe.org, and don't miss our Youth Group Webinar!

❞𝗙𝗲𝗿𝘁𝗶𝗹𝗶𝘁𝘆 𝗮𝗻𝗱 𝗳𝗮𝗺𝗶𝗹𝘆 𝗽𝗹𝗮𝗻𝗻𝗶𝗻𝗴 𝗳𝗼𝗿 𝘆𝗼𝘂𝗻𝗴 𝗽𝗲𝗼𝗽𝗹𝗲 𝘄𝗶𝘁𝗵 𝗹𝘂𝗽𝘂𝘀❞

🌟 What should young people know? What questions do young people have?
🌟 Key information to support informed decisions and future planning

🖥️ In this online webinar, Lupus Europe’s Youth Group will host an open, evidence-based discussion with Prof. Laura Andreoli on lupus, lupus treatments, fertility, pregnancy planning, and reproductive health in young people.

The session will address real questions from young lupus patients, providing clear, practical information to support communication and decision-making between patients and healthcare professionals.

🗣️ Moderated by Jeanette Andersen

Save the date!

🗓️ May 10, 2026
⏰ 19:00 CET (i. e. Paris time)
💻 Zoom
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