The European Alliance of Associations for Rheumatology (EULAR) Congress 2023 was incredibly interesting, full of groundbreaking research and information about lupus! EULAR 2023 was also very successful for Lupus Europe and its Patient Advisory Network (PAN) members. With unwavering dedication and hard work, PAN members showed their commitment to supporting the lupus community across Europe.

 

Alain Cornet Wins PARE Best Abstract Award:

Lupus Europe submitted six abstracts at EULAR Congress 2023. Five of these abstracts were accepted with two selected for oral presentation, including the acclaimed “Lupus Europe’s Patient Advisory Network – A Huge Double Success.” The main author, Alain Cornett, was honoured with the prestigious PARE Best Abstract Award.

 

 

 

 

 

 

 

 

The oral presentation was skilfully delivered by PAN member and Board member, Amy Somers.

 

 

Empowering Patients through Lupus100.org:

One of the resounding successes was the spotlight on the Lupus100 project. The abstract “Lupus100.org – A Step Change in Access to Quality Information for European Lupus Patients” was chosen for an oral presentation in the Opening Abstract Plenary Session of the scientific programme!

The oral presentation was delivered by Zoe Karakikla-Mitsakou. This acknowledgement in the scientific programme underscores the importance of the Lupus100 project in providing valid and easy to understand information about lupus in, currently, more than 80% of the native languages of the European population so lupus patients can access valid information about lupus in their own language.

 

 

 

 

 

The potential of Lupus100 as a tool for patients, but also for doctors was highlighted by Francesca Marchiori (PAN member), Lena Koskina (PAN member) and Alain Cornet through “Lupus100.org a new tool for doctors to build patients lupus knowledge and fight poor quality web information” in the scientific poster tour.

 

 

 

 

 

 

 

 

 

Exploring Crucial Aspects of Lupus:

Alain Cornet’s poster tour presentation “Patient-doctor communication gap – Results of a speed-shop on “lupus flare” at Lupus2022 meetings” highlighted the difference between physicians’ and patients’ definition of a lupus flare.

 

Dalila Tremaria’s (PAN member and Board Member) scientific poster presentation on the “Association between diagnosis delay and disease activity with burden of the disease in 4150 European patients with Systemic Lupus Erythematosus”  put a spotlight on the association between diagnosis delay and self-perceived disease activity with the burden of the disease on the daily life of people living with lupus.

 

 

 

 

 

 

 

 

Furthermore, Jeanette Andersen (Lupus Europe Chair) shared her inspirational journey to the specialists of her rheumatic disease in a captivating fishbowl session!

 

 

 

 

 

 

 

 

 

The abstract “Recommendations on handling medicine shortage: learning from Hydroxychloroquine 2020 crisis for  SLE patients” was also accepted for publication.

 

Enthusiastic Presence at the Lupus Europe Booth:

The Lupus Europe booth was a hub of energy and enthusiasm, thanks to the devoted PAN members who tirelessly manned the booth. Their passion for spreading awareness about Lupus Europe, the Lupus100 project and many other Lupus Europe projects was clear to all those who passed by.

EULAR 2023 Debrief – For People Living with Lupus” Webinar:

Lupus Europe invites you to watch the joint Lupus Europe / ERN ReCONNET webinar on “EULAR 2023 Debrief – for people living with lupus”. Watch the webinar to learn more about Lupus Europe successes at EULAR Congress 2023, hear first-hand from PAN members who took part in the Congress, but also to discover more about the ground-breaking presentations and initiatives that made EULAR 2023 an extraordinary success.

 

Watch the webinar at the Lupus Europe Website Library or by following this link: https://www.lupus-europe.org/videos-on-demand/#iframe-1 

 

 

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4 days ago

🚨 𝐋𝐚𝐬𝐭 𝐝𝐚𝐲 𝐭𝐨 𝐜𝐨𝐦𝐩𝐥𝐞𝐭𝐞 𝐭𝐡𝐞 𝐬𝐮𝐫𝐯𝐞𝐲❗

📈 In 2020, our "Living with Lupus" survey revealed the significant burden and vast differences in #SLE care across Europe from the patient's perspective.

🔊These findings have become invaluable to lupologists worldwide, shaping how this complex disease is understood and managed.

🎯 The insights from this new survey aim to build on the previous data, helping to refine treatment approaches and care strategies.

‼️ Your participation is crucial in providing a comprehensive view of the current challenges and needs faced by those living with lupus.

✅ The results will not only assist physicians but also inform patients and policymakers, playing a key role in advancing lupus care and advocacy efforts. This is your chance to contribute to a better understanding of lupus and to ensure that care strategies are as effective and tailored as possible.

🕒 Complete this anonymous survey before May 15th and help us capture the diverse experiences of individuals affected by lupus across Europe.

🌐 Available in 21 Languages:

🇨🇿 Czech s.surveylegend.com/-NtkhoZPH8WNeA5e2ZCC
🇩🇰 Danish s.surveylegend.com/-NqmjTjyUXHGLMmAu5qS
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🇪🇸 Spanish s.surveylegend.com/-Nudx9pGv-1XtZ6OnYWs
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4 days ago

‼️ #Lupus is more than a disease with physical symptoms such as pain and fatigue; it's an illness that can influence every part of your life.

⚠️ #SLE can potentially affect a wide range of daily activities, from educational pursuits and career development to maintaining family relationships and social activities.

✅ That is one of the reasons why you have to complete the "Living with Lupus in 2024" survey: to understand the real-world impact of lupus to be able to advocate for better support, care, and treatment options.

🌟 Your insights are invaluable in shaping effective interventions and enhancing support systems for everyone affected by this complex condition in Europe.

🙏 Don't miss this unique opportunity to advocate for change and push for advancements in how lupus is managed and treated, ensuring that every individual receives the care they deserve.

🔗 Click on this link and select your language: s.surveylegend.com/-Nr54WsZrcnC-4BwDBrG
... See MoreSee Less

‼️ #Lupus is more than a disease with physical symptoms such as pain and fatigue; its an illness that can influence every part of your life.

⚠️ #SLE can potentially affect a wide range of daily activities, from educational pursuits and career development to maintaining family relationships and social activities.

✅ That is one of the reasons why you have to complete the Living with Lupus in 2024 survey: to understand the real-world impact of lupus to be able to advocate for better support, care, and treatment options.

🌟 Your insights are invaluable in shaping effective interventions and enhancing support systems for everyone affected by this complex condition in Europe.

🙏 Dont miss this unique opportunity to advocate for change and push for advancements in how lupus is managed and treated, ensuring that every individual receives the care they deserve.

🔗 Click on this link and select your language: https://s.surveylegend.com/-Nr54WsZrcnC-4BwDBrGImage attachmentImage attachment+1Image attachment
6 days ago

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

✍🏻 Izpolnite anketo.

🔊 Delite z vašo skupnostjo.

🙏 Help us achieve more answers to ensure the Slovak population is represented in the results

s.surveylegend.com/-Nt-wdNdIqT4v3ptXEM1

#lupusawarenessmonth
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1 week ago

🦋 #WorldLupusDay is coming to an end!

❤️ Thank you all for the support you have shown throughout this important day in which the whole world has raised awareness of the impact that lupus can potentially have 💥.

🌈 However, we at Lupus Europe believe that there is something very important that we also need to show the world: our vitality, our energy, and our will to enjoy life – including our work.

🌟 Our strong vision in a fulfilling life for all people with lupus in Europe, until we have reached a world without lupus.

😃 We always work hard! We all have lupus, though our amazing Lupus Europe family seems to forget about it when we are at an event, a meeting, or are working for the organisation.

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

🌺 Every day, but especially this # WorldLupusDay, we thank all those who stand by our side and show the best face of the 1000 faces lupus has.
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LUPUS EUROPE Uniting people with Lupus throughout Europe
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