In 1989, LUPUS EUROPE (then named ELEF)’s first convention took place in the historical city of Leuven. 29 years later, LUPUS EUROPE’s 2018 annual convention brought us back to the place of our beginnings. The 2018 convention theme was “Restoring Hope”. Lupus is not always easy to deal with and we can often feel down: when a flare is painfully reminding us of the disease; when one more clinical trial fails; when we feel tired and misunderstood… As leaders in patient groups, we also regularly receive calls for help from people who are so scared after just being diagnosed, or who face depression. It is so easy to lose hope when you have lupus…. Yet there are reasons to keep hope: the search for new medication is more active than ever; patients are becoming more involved handling their own disease; lupus awareness is growing; legislation in support of people with disabilities (visible or not) is progressing; and patient support groups are bringing hope to their members in many different ways.

A total of 37 member delegates, coming from Belgium (5), Cyprus (2), Denmark (3), Finland (2), France (3), Italy (4), Lithuania (2), Netherland (3), Portugal (2), Slovakia (1), Sweden (1), UK (7), Switzerland (1), and Israel (1) joined the convention this year, making it a record number of participants.

Our program gave a very large place to interactions between participants, with 15 different workshops on various topics centered on the “restoring hope” theme. Participants defined and selected themselves the themes that they had most interest for, including how patients can better participate to research, making the web more positive, Giving inspiring life stories, or enjoying the small things in life.

We obviously reviewed the activities of lupus Europe in 2018, and in our council session, renewed the board and set the direction for 2019. Several external speakers gave us additional insights on the theme of “restoring hope” : Professor Houssiau, chair of the European Lupus Society addressed the recent medical developments, and the reasons to hope they provide;  Bernadette Van Leeuw, Chair of Lupus Belgium (French speaking group) highlighted the importance of action to make better things indeed happen as a key component of hope; Torben Wiese, inspirational speaker, invited us to all become change agents; and Nele Cayers (Chair of PARE) explained how we can achieve better results by leveraging the broader EULAR community. The convention closed with an excellent seminar from Sylvia Gauman (Swiss delegate)on improving our communication with Journalists…

A detailed convention report can be downloaded here: Leuven 2018. You can also find here convention reports from prior years: Milan 2017Wurzburg 2016 and Vienna 2015

 

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4 hours ago

🌍 This #WorldLupusDay, take part in a unique event specially tailored for young people living with lupus:

😃 "Lupus and Youth: A Dialogue between the Lupus Europe Youth Group and a Young Rheumatologist".

📆 May 10th.
🕖 19:00 CET (i. e. Paris time).

‼️ This is not just any webinar for the youth. It is a webinar made by youth for youth.

👀 So expect anything! This is why you cannot miss this date, whether you are young or not: understanding the worries and needs of young people with lupus is key to addressing their needs.

📧 Join us! Send an e-mail to secretariat@lupus-europe.org and secure your spot now.

www.lupus-europe.org/lupus-europe-youth-webinar/
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🌍 This #WorldLupusDay, take part in a unique event specially tailored for young people living with lupus:

😃 Lupus and Youth: A Dialogue between the Lupus Europe Youth Group and a Young Rheumatologist.

📆 May 10th.
🕖 19:00 CET (i. e. Paris time).

‼️ This is not just any webinar for the youth. It is a webinar made by youth for youth.

👀 So expect anything! This is why you cannot miss this date, whether you are young or not: understanding the worries and needs of young people with lupus is key to addressing their needs.

📧 Join us! Send an e-mail to secretariat@lupus-europe.org and secure your spot now.

https://www.lupus-europe.org/lupus-europe-youth-webinar/

✅ While it's true that 9 out of 10 individuals diagnosed with #lupus are women, it's crucial to also reflect on the significant impact this disease has on men. Lupus does not discriminate, and understanding its effects on all genders is vital.

🌍 𝗠𝗲𝗻 𝗺𝗮𝘆 𝗳𝗮𝗰𝗲 𝘂𝗻𝗶𝗾𝘂𝗲 𝗰𝗵𝗮𝗹𝗹𝗲𝗻𝗴𝗲𝘀 𝗮𝗻𝗱 𝘀𝘆𝗺𝗽𝘁𝗼𝗺𝘀 that can differ from those typically reported by women and that is why we have included a specific section for men with lupus that has been created by men with lupus.

🇪🇺 If you are a 𝗺𝗮𝗻 𝗹𝗶𝘃𝗶𝗻𝗴 𝘄𝗶𝘁𝗵 𝗹𝘂𝗽𝘂𝘀 𝗶𝗻 𝗘𝘂𝗿𝗼𝗽𝗲, your participation in this survey is essential to help us better understand how lupus affects men.

Your insights can lead to better support and more effective interventions for all men affected by lupus.

🔊 Remember! This anonymous survey is available in 21 languages and will take no more than 10 minutes to complete.

buff.ly/3UMZkAQ
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2 days ago

♦️ Few days left to fill the Living With Lupus in 2024 survey!

✍🏻Weź udział w ankiecie.

🔊Udostępnij w swojej społeczności.

🙏 Help us and Lupus Poland achieve more answers to ensure that the Polish population is represented in the results

s.surveylegend.com/-Nr1vl1sxwISBcDaeOzP
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5 days ago

♦️ Few days left to fill the survey!

✍🏻 Realiza la encuesta.

🔊 Comparte con tu comunidad.

🙏 Help us and Felupus ensure the Spanish population is represented

s.surveylegend.com/-Nudx9pGv-1XtZ6OnYWs
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