🎥 Have questions about the new systemic lupus erythematosus (SLE) guidelines? Following yesterday's #ACR25 session, Dr. Lisa Sammaritano, rheumatologist at Hospital for Special Surgery and Principal Investigator for the American College of Rheumatology’s SLE Guidelines team, shared insights on what’s new, what’s changed, and how these updates will shape #lupus care moving forward. Watch the video and read more: https://buff.ly/nxiWOHq | Lupus Foundation of America
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🎥 Have questions about the new systemic lupus erythematosus (SLE) guidelines? Following yesterday's #ACR25 session, Dr. Lisa Sammaritano, rheumatologist at Hospital for Special
Lupus Foundation of America. . 🎥 Have questions about the new systemic lupus erythematosus (SLE) guidelines? Following yesterday's #ACR25 session, Dr. Lisa Sammaritano, rheumatologist at Hospital for Special Surgery and Principal Investigator for the American College of Rheumatology’s SLE Guidelines team, shared insights on what’s new ...
825 views2 weeks ago
Lupus Foundation of America What is Lupus
Following the U.S. Food and Drug Administration’s approval of Gazyva® (obinutuzumab) for the treatment of adults with #lupus nephritis, Dr. Brad Rovin, Chair of the Lupus Foundation of America’s Medical-Scientific Advisory Council and investigator in the REGENCY trial, shares what this milestone means for people with lupus. 🎥 Hear his insights and learn more in our new resource answering what you need to know about Gazyva: https://buff.ly/9CFUWAS | Lupus Foundation of America
Following the U.S. Food and Drug Administration’s approval of Gazyva® (obinutuzumab) for the treatment of adults with #lupus nephritis, Dr. Brad Rovin, Chair of the Lupus Foundation of America’s Medical-Scientific Advisory Council and investigator in the REGENCY trial, shares what this milestone means for people with lupus. 🎥 Hear his insights and learn more in our new resource answering what you need to know about Gazyva: https://buff.ly/9CFUWAS | Lupus Foundation of America
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6K views3 weeks ago
355 reactions · 183 shares | Lupus is a cruel mystery—but together, we can solve it. With RAY: Research Accelerated by You, people with lupus and caregivers can share their experiences on the Lupus Foundation of America's online patient registry and help researchers develop new treatments. Sign up today to be the solution to lupus! | Lupus Foundation of America | Facebook
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355 reactions · 183 shares | Lupus is a cruel mystery—but together, we can solve it. With RAY: Research Accelerated by You, people with lupus and caregivers can share their experiences on the Lupus Foundation of America's online patient registry and help researchers develop new treatments. Sign up today to be the solution to lupus! | Lupus Foundation of America | Facebook
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6K views2 weeks ago
4.1K views · 4.3K reactions | Has lupus touched your life or family? Do you have questions about this cruel & complex disease? We have resources for you! This Lupus Awareness Month, we can all help bring attention to this mysterious disease. Learn more today. | Lupus Foundation of America | Facebook
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4.1K views · 4.3K reactions | Has lupus touched your life or family? Do you have questions about this cruel & complex disease? We have resources for you! This Lupus Awareness Month, we can all help bring attention to this mysterious disease. Learn more today. | Lupus Foundation of America | Facebook
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Hi LupusChick family! Marisa here with some updates. For starters, LupusChick is growing so much and we can't thank you all enough for your constant support and sharing of our content. We are undergoing a full rebrand this summer with a new website that will go along with my memoir coming out next year from Broadleaf Books. We have a ton of new resources and goodies that we cannot wait to share with you. We are also going to have an amazing shop full of items I specifically picked to help us get
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Hi LupusChick family! Marisa here with some updates. For starters, LupusChick is growing so much and we can't thank you all enough for your constant support and sharing of our content. We are undergoing a full rebrand this summer with a new website that will go along with my memoir coming out next year from Broadleaf Books. We have a ton of new resources and goodies that we cannot wait to share with you. We are also going to have an amazing shop full of items I specifically picked to help us get
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🦋 Welcome to Lupus Awareness Month 2024! 🦋 May is Lupus Awareness Month, a time to learn about the struggles faced by those with lupus and work for change. Lupus is a complex chronic autoimmune disease that affects individuals of all ages and backgrounds, yet its cause remains unknown, and a cure is still elusive. Our campaign this May is ‘Raising Awareness, Inspiring Change’, we hope to bring attention to the socioeconomic impacts of living with lupus in Canada, emphasizing the need for equit
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🦋 Welcome to Lupus Awareness Month 2024! 🦋 May is Lupus Awareness Month, a time to learn about the struggles faced by those with lupus and work for change. Lupus is a complex chronic autoimmune disease that affects individuals of all ages and backgrounds, yet its cause remains unknown, and a cure is still elusive. Our campaign this May is ‘Raising Awareness, Inspiring Change’, we hope to bring attention to the socioeconomic impacts of living with lupus in Canada, emphasizing the need for equit
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From the onset of symptoms, it takes an average of six years to get an accurate lupus diagnosis. We’ll be with you every step of the way. Visit the National Resource Center on Lupus for more information about symptoms and treatment options. | Lupus Foundation of America
From the onset of symptoms, it takes an average of six years to get an accurate lupus diagnosis. We’ll be with you every step of the way. Visit the National Resource Center on Lupus for more information about symptoms and treatment options. | Lupus Foundation of America
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March is #AutoimmuneAwarenessMonth. Let's shed light on lupus, an autoimmune disease affecting millions worldwide. Common symptoms include extreme fatigue, joint pain, skin rashes, fever and more. Help us spread awareness this month by watching and sharing our brief video. | Lupus Foundation of America
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March is #AutoimmuneAwarenessMonth. Let's shed light on lupus, an autoimmune disease affecting millions worldwide. Common symptoms include extreme fatigue, joint pain, skin rashes, fever and more. Help us spread awareness this month by watching and sharing our brief video. | Lupus Foundation of America
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Most symptoms of lupus aren’t often visible, but can affect every aspect of someone’s life physically, mentally and emotionally, relationships etc. Just because people can't see the impacts of lupus, doesn't mean they don’t exist - help us Make Lupus Visible this Lupus Awareness Month! | Lupus Foundation of America
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Most symptoms of lupus aren’t often visible, but can affect every aspect of someone’s life physically, mentally and emotionally, relationships etc. Just because people can't see the impacts of lupus, doesn't mean they don’t exist - help us Make Lupus Visible this Lupus Awareness Month! | Lupus Foundation of America
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Hi LupusChick family! Marisa here with some updates. For starters, LupusChick is growing so much and we can't thank you all enough for your constant support and sharing of our content. We are undergoing a full rebrand this summer with a new website that will go along with my memoir coming out next year from Broadleaf Books. We have a ton of new resources and goodies that we cannot wait to share with you. We are also going to have an amazing shop full of items I specifically picked to help us get
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