As #LupusAwarenessMonth comes to a close, we're inspired by the resilience and strength of the #lupus community. At Alumis, we're honored be part of the research community dedicated to advancing effective treatment options for people living with lupus. We recognize the global impact of lupus and will continue to focus on the advancement of our lupus clinical program with the goal of make a difference for the lupus community worldwide! #LupusAwareness #LupusResearch
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Why we're doing what we're doing. #lupus #lupusawareness #digitalhealth #mhealth #patientengagement #patientreportedoutcomes #realworldevidence #realworlddata
What fuels our passion for lupus research? 🔬 Since 2020, our mission has been to better understand the needs of people living with lupus and their clinicians, innovating solutions to enhance the quality of life for those affected by this incredibly difficult condition. But what motivates us on this journey? Find out directly from our brilliant team below 👇 Dr Max Noble, Dr Frances Pearson, Jadie Acklam, Dr Claire Tkacz, Anna Longjaloux #lupusawareness #lupusresearch #lupus #rarediseaseday2024
What motivates VISFO to work in lupus
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LUPUS EUROPE is conducting a survey to gather insights into the experiences of individuals living with #lupus across Europe. 🌍 In 2020, Lupus Europe launched a large “Living with lupus survey”. Thanks to the huge participation from patients around Europe, the insights from this survey are largely used. Time has now come for a new survey, with different topics, to add to our knowledge of what it means to live with lupus in 2024. The survey is anonymous and should take approximately 10 minutes to complete. It is available in 19 different languages. Click the following link to complete the survey: https://lnkd.in/eA8A57sh 🔗 Thank you for sharing your views! #LupusAwareness #LupusResearch #SLE #LupusCommunity #LupusEurope
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We’re sharing the experiences of remarkable individuals like Annemarie Sluijmers, who is living with lupus. Her journey goes beyond a diagnosis; a powerful testament to resilience. Join us in this conversation and help us spread awareness and support for those affected by lupus. Dive into the stories, engage with the facts, and be part of the change. Visit www.Lupus100.org, developed by LUPUS EUROPE to learn more about lupus. #MakeLupusVisible #LupusAwareness #Lupus100
Annemarie Sluijmers
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WORLD LUPUS DAY: The time is now to pursue remission as a key care goal in lupus. Aligned with the latest clinical recommendations, we can aim to reduce reliance on oral corticosteroids and work to build a future where remission is possible for more people living with lupus. This World Lupus Day, learn more about how we’re following the science to help make remission a reality: https://bit.ly/3Wt2QkT #WorldLupusDay #MakeLupusVisible
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Dear Lupus Specialists, Our latest Literature Highlights for October are here! Stay updated with the most significant lupus studies and findings. Access the insights you need to advance your expertise in treating lupus. https://lnkd.in/dDQbCijZ Your dedication to lupus research is making a real impact. Share this resource with your colleagues and let's keep pushing the boundaries of our understanding and care. #LupusResearch #LupusSpecialists #MedicalResearch
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On World Lupus Day, we bring to light the personal battles and triumphs of those living with lupus. It’s a day to share patient stories that inspire and educate, like those of Hronn Stefansdottir and Annemarie Sluijmers, who have faced lupus with incredible bravery and grace. Their narratives are a powerful reminder of the resilience that defines the human spirit. Visit http://ms.spr.ly/6045Yn6a7 to learn more about lupus. Let’s work together to make lupus visible and support the lupus community worldwide. #WorldLupusDay #MakeLupusVisible #AsOneForPatients #PatientDirected #LupusAwareness #Lupus100
World Lupus Day
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🔥 There has been a lot of hype about a lupus discovery that could lead to better treatments and possibly "a cure." Join us next Saturday, July 27, 5PM EST on FaceBook to discuss this topic. (go to the More Than Lupus page at that time, and click on the live video feed) Go to this link and click on "Going": https://lnkd.in/e_rRS-xf 👉 I'll put things in true perspective 👉 I'll give advice that patients can use to better understand news hype like this, which pops up now and then 👉 I'll go over some actual, really exciting new lupus information that patients can put to use immediately (studies that should be hyped up more than it is) Thanks to More Than Lupus
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Have you discovered Inside Lupus Research? It’s your go-to source for the latest and most significant lupus research news. Stay informed with current headlines and subscribe to receive updates directly in your inbox! Check out the latest here: https://lnkd.in/en9zHa4N #lupusresearch #lupus
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Today, on #WorldLupusDay, we shine a spotlight on lupus, a complex #autoimmunedisease affecting millions worldwide. Together, we can advocate for better research, treatments, and support systems. 💜 #LupusAwareness
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The results are in! From our Facebook and Instagram poll, we determined your biggest inquiry is, "Where can I find more information about lupus?" Thankfully, we have THE lupus expert Dr. Don Thomas here to help! He will be joining us in September to respond to each of the most asked questions. More details to come!!!
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