Welcome to
Our Lupus Community

Welcome to the Lupus Community, where we provide support, resources and a community for those affected by lupus. Whether you're a patient, caregiver, or advocate, you're not alone in this journey. Join us today to connect with others, share experiences, and access valuable information.

Lupus 100

Learn how Lupus 100 is making a difference in the fight against lupus. Support our mission to raise awareness and funds for lupus research. Click here to visit Lupus 100 and join the cause.

Lupus Europe

Discover how Lupus Europe empowers patients and advocates for better healthcare. Join us in supporting lupus patients across Europe. Visit our page to learn more and get involved.

NATIONAL LUPUS GROUP MEETING

Lupus UK

Join us for our weekly Lupus UK meetings in London. These meetings provide a supportive environment where you can connect with others, learn more about managing lupus, and access valuable resources. Whether you’re newly diagnosed or have been living with lupus for years, everyone is welcome.

2024 National Lupus Advocacy Summit

London, UK
March 13, 2024, Wednesday,
6:00 PM – 8:00 PM

2024 National Lupus Advocacy Summit

London, UK
March 13, 2024, Wednesday,
6:00 PM – 8:00 PM

2024 National Lupus Advocacy Summit

London, UK
March 13, 2024, Wednesday,
6:00 PM – 8:00 PM

JOIN OUR LUPUS COMMUNITY

Join our community to connect with others, share your story, and access resources.
Whether you’re seeking support or looking to support others, you’ll find a welcoming community here.

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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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