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Latest blogs

Charles Bridge in Prague at sunset with historic towers and colourful buildings under a dramatic sky.
National Member News – Hello from the Czech Republic
October 29, 2024
Lupus patient holding a medal for the 5km Run Limassol 2024 race.
My Dream to Run– A lupus Patient’s Dream Come True!
May 20, 2024
Join the Conversation: Lupus Europe’s Youth Webinar for World Lupus Day
May 6, 2024
Sunset view of the Motlawa River embankment with historical buildings in Gdansk, Poland.
National Member News – Hello from Poland
March 18, 2024
Rare Disease Day 2024 banner with people from diverse backgrounds and colourful handprints symbolising global unity and awareness for rare diseases
Rare Disease Day 2024!
February 29, 2024
Detailed close-up of skin texture, representative of the dermatological focus in skin lupus studies
Stepping Up for Skin Lupus: An ePAG in ERN Skin
January 8, 2024

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Latest Videos

Mitochondria in Systemic Lupus Erythematosus (SLE)
Mitochondria in Systemic Lupus Erythematosus (SLE)
Oct 24, 2022
Sjögren's Syndrome in Lupus: Does it Change Anything?
Sjögren's Syndrome in Lupus: Does it Change Anything?
Oct 24, 2022
Non-Atherosclerotic Cardiovascular Disease in SLE and APS
Non-Atherosclerotic Cardiovascular Disease in SLE and APS
Oct 24, 2022
70 Years Learning to Use Glucocorticoids
70 Years Learning to Use Glucocorticoids
Oct 24, 2022
Refractory Skin Manifestations in Lupus
Refractory Skin Manifestations in Lupus
Oct 24, 2022
Risk Gene Linked to Cardiovascular Disease
Risk Gene Linked to Cardiovascular Disease
Oct 24, 2022

Lupus Europe Follow 6,770 4,076

Lupus Europe is the umbrella association of currently 32 national lupus self-help organisations throughout Europe, and supports people with lupus in Europe.

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LUPUS EUROPE
2 days ago
LUPUS EUROPE

🦋 #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. ... See MoreSee Less

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LUPUS EUROPE
2 days ago
LUPUS EUROPE

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

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

#WorldLupusDay
#Lupus100 ... See MoreSee Less

‼️ It is estimated that about 50% of #SLE patients will suffer from #lupus nephritis, one of SLEs most dangerous & frequent complications. 💊 Routine checkups and available treatments make it possible for 60–70% of patients to achieve complete or partial remission. #WorldLupusDay #Lupus100
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LUPUS EUROPE
2 days ago
LUPUS EUROPE

🔴 Despite significant improvements in diagnosis delay & treatment strategies, the burden of #SLE remains high.

Learn more on the association between diagnosis delay, disease activity and burden on daily life in patients with #lupus in this study: lupus.bmj.com/content/8/1/e000469

And get to better understand how to live with #lupus thanks to #Lupus100! A website written by doctors and patients to make it possible for people with lupus to have easy-to-understand and high-quality information about lupus!

lupus100.org/en/100-questions#Challenges

Need more? Check out #LupusGPT! lupusgpt.org/

#WorldLupusDay
#Lupus100 ... See MoreSee Less

🔴 Despite significant improvements in diagnosis delay & treatment strategies, the burden of #SLE remains high. Learn more on the association between diagnosis delay, disease activity and burden on daily life in patients with #lupus in this study: https://lupus.bmj.com/content/8/1/e000469 And get to better understand how to live with #lupus thanks to #Lupus100! A website written by doctors and patients to make it possible for people with lupus to have easy-to-understand and high-quality information about lupus! https://lupus100.org/en/100-questions#Challenges Need more? Check out #LupusGPT! https://lupusgpt.org/ #WorldLupusDay #Lupus100
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LUPUS EUROPE
2 days ago
LUPUS EUROPE

🚨 #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.

Do you want to know what the first symptoms of #lupus are?

Visit #Lupus100 and #lupusgpt and find out!

Getting to know the disease is key for an early diagnosis.

lupus100.org/en/questions/what-are-the-first-signs-of-lupus

lupusgpt.org/

#WorldLupusDay
#MakeLupusVisible ... See MoreSee Less

🚨 #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. Do you want to know what the first symptoms of #lupus are? Visit #Lupus100 and #LupusGPT and find out! Getting to know the disease is key for an early diagnosis. https://lupus100.org/en/questions/what-are-the-first-signs-of-lupus https://lupusgpt.org/ #WorldLupusDay #MakeLupusVisible
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3 CommentsComment on Facebook