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Fatigue is the most prevalent and incapacitating symptom experienced by about 85 to 92% of people with #lupus, resulting in decreased physical and mental function, and 50% of patients rated it as the most disabling symptom. #LupusAwarenessMonth #LupusAwareness #LupusChat

Intriguing to hear from Dr. Lipsky yesterday that there is some hope that AI can improve the way we approach patient care. There are some roadblocks of course but the prospective looks somewhat promising. #LUPUS25 #LADAOrg #LupusChat

#LADAORG Pediatric Scientific Session: Outcomes and Targets in Children with SLE Andrea M Knight: Targets for the Management of NPSLE (Including Mental Health) #LUPUS2025 #LupusChat #Lupus

In this photo the happiness of being part of this wonderful Congress with people who speak the same language (lupus, not Italian 🤣) and our contribution in studying #cognitivedysfunction in #lupus #brainfog #lupus2025 Matteo Piga

Thank you to everyone who joined us for an incredible Day 2 of #LUPUS2025! 🌟 Your passion, insights & energy made it unforgettable. We can’t wait to welcome you back tomorrow for another inspiring day filled with innovation, learning & connection. 💜 See you in the morning!

💜May is #lupusawarenessmonth. Did you know that Lupus in children is often more severe than in adults? #Lupus can impair growth, delay puberty, and shorten life expectancy—disrupting a child’s development, education, and mental health.

Why follow antiDNA and complements in #lupus #nephritis #LN #LUPUS2025 panel said To detect flare ?to consider after 3 to 5 yrs of remission to taper Rx ?but not for early response to Rx Just info from the panel with my opinion salted in Dr. John Cush

#LADAorg Poster 145 THE UNMET NEEDS OF LUPUS PATIENTS: CREATING VISIBILITY AND SUPPORTING PATIENTS AND FAMILIES IN THEIR JOURNEY "Ghana has three Rheumatologists to a population of over 33 million" Oyemamautoimmune Donald Thomas, MD #Lupus2025 #Lupuschat #Lupus

Patient session #LUPUS2025

🚨 ERN ReCONNET - SLICC - SLEuro expert #consensus on the therapeutic management of RARE systemic #lupus erythematosus manifestations ⬇️ CHECK LINK: doi.org/10.1016/S2665-…

#LADAorg Lupus Nephritis #Lupus2025 #LupusChat #Lupus

Couldn’t miss Laurent ARNAUD’s session on Rare SLE Manifestations! 🔹final list of 45 rare SLE manifestations 🔹21 selected for potential treatment strategies 🔹strategies include treatment for both severe & non-severe cases Read more here thelancet.com/journals/lanrh… #LUPUS2025

Up to 95% of #SLE patients have joint involvement. Lupus arthritis remains challenging to assess due to its fleeting nature. Updated classifications (1998 vs 2019) include imaging-based forms: RA-like, Jaccoud’s, NDNE, and even psoriatic-like. #LUPUS2025

🚨🚨🚨 AHHH we have just been granted a 🔓 FREE 50-DAY ACCESS LINK to the expert #consensus on the therapeutic management of RARE systemic #lupus erythematosus manifestations Can you please re-tweet the link so that a MAXIMUM have access for free 🔄 LINK: authors.elsevier.com/a/1l8og9UBHvvg…

It’s so great meeting new people at conferences, but running into people you met at previous conferences is special 💜 #LADAorg

It is estimated that as many as one in every 250 African American women in America has #lupus and huge health disparities exist. There is a critical need for #socialdeterminants of health (SDOH) to be addressed as well. #LupusAwarenessMonth #LupusAwareness #LupusChat CoLN

Lupus 2025 Thank you for an amazing and informative experience! Our Lupus Association Team found it to be very rewarding! #LupusChat Caring For Lupus CoLN Tiffany ⁷ Whitney Carter LaBar🎗👊, Chronically Awesome Kaamilah Gilyard Autumn Austin (Lupus Guru) Zahi Touma, MD, PhD

The annual per patient cost to employers, including medical care, work absence, and shortterm disability, is higher than for other chronic diseases such as diabetes, chronic obstructive pulmonary disease, and heart disease. #LupusAwarenessMonth #LupusChat Caring For Lupus

💚 May is Arthritis Awareness Month. Many people don't realize that arthritis affects children - causing pain and other problems, limiting physical activity, and resulting in frequent doctors' appointments. Juvenile Idiopathic Arthritis is an autoimmune disease that has no cure.

#LupusAwarenessMonth 2025 ends today but we must continue to promote #LupusAwareness in order to gain support for critical #Lupus Education, Advocacy and Research Programs to improve lives. Thank you to all who liked and shared our 31 Days of Lupus Facts, we appreciate you! 💜🦋