Patient Solidarity Day – IAPO

  The 3rd of December is Patient Solidarity Day. Support IAPO’s (International Alliance of Patient Organisations) Thunderclap through your social media accounts by clicking here: http://thndr.me/7mJakT For more information on what a Thunderclap is and how to use it, click here. The aim is to reach at least 100 supporters on Thunderclap, otherwise the message won’t be shared on […]

New York Marathon – Andreas

We are nearly there, Andreas Panteli will be running for LUPUS EUROPE in the New York Marathon on 6th November. Experience the World’s Biggest Marathon You can catch the excitement of the TCS New York City Marathon from anywhere on the planet. In the New York tri-state area, the race broadcasts live on WABC-TV, Channel […]

LUPUS EUROPE convention report

For those of you who may have missed it or who are not signed up on our mailing list, here is the link to the convention report for LUPUS EUROPE’s annual convention which was held this year from 28th September – 2nd October 2016. If you don’t currently receive our newsletters and emails and would like […]

Nearly there – Andreas running for lupus

2 weeks to go, Running for Lupus Hej, Tere, Hei, Χαιρετώ, Bonjour, Hallo, Helló, Ciao, Olá, Ahoj, Hallå, Hola, Grüezi, Halló, Dia dhuit, Shalom, As-salam alaykom, Buna, Sveiki, Zdravo Many things have happened since the last blog post. As you can see in the above picture, the t-shirt design has been finalised and ordered for printing. You will […]

World Arthritis Day – EULAR conference on reducing the burden of chronic diseases in the workplace

Today is World Arthritis Day. A day being honoured by The EULAR Conference on reducing the burden of chronic diseases in the workplace for people with RMDs. The conference is focusing on identifying and discussing relevant issues related to the working environment and how to move forwards. The conference was opened by EULAR president Prof. Gerd R. […]

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🦋 #WorldLupusDay is coming to an end!

❤️ Thank you all for the support you have shown throughout this important day, as people around the world have come together to raise awareness of the impact lupus can have.

🌈 At Lupus Europe, we believe there is something very important we also need to show the world: our vitality, our energy, and our will to enjoy life, take part, contribute, and be heard.

🌟 Our vision is a fulfilling life for all people with lupus in Europe, until we reach a world without lupus.

😃 We work hard. We show up. We support each other. We all live with lupus in different ways, even if our amazing Lupus Europe family sometimes seems to forget about it when we are at an event, in a meeting, or working together for the organisation.

🦋 Lupus is an invisible illness with many faces. Let’s close this #WorldLupusDay with our hopes, our laughter and our enthusiasm for life.

💬 That is why today we also want to remind you of our #MakeItCount campaign and the 𝐋𝐮𝐩𝐮𝐬 𝐂𝐨𝐧𝐬𝐮𝐥𝐭𝐚𝐭𝐢𝐨𝐧 𝐂𝐚𝐫𝐝𝐬.

These cards are designed to help people living with lupus prepare for medical appointments, organise their thoughts, identify what matters most, and make consultations more focused and meaningful.

🌺 Visit our website, download the Lupus Consultation Cards, and use them at your next appointment.

www.lupus-europe.org/lupus-consultation-cards/

Because your priorities, questions, and needs deserve a place in every consultation.
Let’s #MakeItCount.
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💜 Thank you to everyone who joined our Youth Group webinar on fertility, family planning & lupus today!

Important conversations like these help tackle fears, misconceptions & unanswered questions around lupus and reproductive health.

🦋 Don't forget to include this topic in the Lupus Consultation cards in your next appointment!

#MakeItCount. Check out this new tool that helps patients prepare for consultations and improve communication with healthcare professionals.

Available in many languages!

📌 Download here:
www.lupus-europe.org/lupus-consultation-cards/
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