Friends AgainstLupus

A new study reviews advancements, including remission and drug therapy discontinuation, in people with #lupus treated with CAR-T therapy. The treatment shows promise in altering disease prognosis. Read the study: buff.ly/kahdrXF

Tiffany was one of the people who helped me with my readathon. I’m so appreciative of you and the work you do! @TiffanyAndLupus 💜🦋

It’s the first day of #LupusAwarenessMonth, & we’re so excited! All month long, we’ll be raising awareness, hosting chats, and making lupus visible. #LupusChat is proud to stand strong, speak loud, & facilitate spaces dedicated to health literacy. Watch this space for updates! 💜

✅ Every year, May is #LUPUSAWARENESS month - a UNIQUE opportunity to raise awareness about this rare #autoimmune disease - and make people understand the diversity, complexity, and for some the MAJOR IMPACT of #Lupus upon daily life 🦋

Proud to support #LupusTherapeutics and the @LupusResearch in advancing #LupusClinicalResearch! Join their Virtual Summit May 5, 4–6pm EST, exploring cell therapy's exciting role in lupus care. 👉 Register: bit.ly/4bZYho4 #LuCINCommunity #CellTherapy #Lupus

#Lupus is a complex chronic inflammatory autoimmune disease in which a triggering agent causes the immune system to dysregulate, attacking any organ system of the body; including the skin, joints, kidney, brain, heart, lungs, blood & blood vessel. #LupusAwarenessMonth

En @LupusAcleg , celebramos el 10 de Mayo #DML a las 18h por ZOOM con una charla de @olgatgn de @MAS_Clinic "Resolviendo dudas sobre la Hidroxicloroquina en el Lupus". @Felupus @GSK_ES y os dejamos el LINK. ⬇️ google.com/url?q=https://…

🌈 Recuerda q se puede ser madre teniendo una enfermedad reumática como el #lupus. 🙏 Habla con tu médico sobre ello porque, como bien dice @SEReumatologia, #HoySíPuedo 🤰Escucha el testimonio d Nuria y no pierdas la esperanza f.mtr.cool/okccrymeem #30DíasLupus #DíaDeLaMadre

#Lupus clinical research has been problematic due to the lack of basic understanding of the disease, reliable biomarkers, and uniform control groups, clinical outcome measure limitations and the heterogeneity of the patient population. #LupusAwarenessMonth #LupusAwareness

✅ Do you have #LUPUS and #BRAINFOG? If so, we would like to INVITE YOU to contribute to our research STUDY for the development of the Lupus Brain Fog Severity Scale - a questionnaire to assess the characteristics and severity of brainfog in lupus 🦋 LINK:lupusresearch.limequery.org/697679?lang=en

Do you have #LUPUS and #BrainFog? Help us develop the Lupus Brain Fog Severity Scale—a validated questionnaire to measure brain fog severity in lupus. Your input is essential. Please participate today & RT to share. More info ⬇️⬇️

🦋Quieres ser madre y tienes #lupus? Planificar el 🤰con tu médico es d vital importancia. Hay q evaluar tu estado d salud, posibles riesgos y revisar la medicación. 👩‍⚕️ Es aconsejable q el lupus esté en remisión al menos 6 meses antes d la concepción #30DíasLupus #DíaDeLaMadre

Fatigue, pain or swelling in joints, skin rashes and fevers could be signs of #lupus. Knowing these symptoms can be helpful in getting diagnosed. This #LupusAwarenessMonth, #ManyOneCan learn more about Lupus Research Alliance and how to educate your community about lupus by visiting: bit.ly/ManyOneCan2025

‼️El lupus afecta a cada paciente d un modo distinto. 🎢Sus 𝐬𝐢́𝐧𝐭𝐨𝐦𝐚𝐬 varían en intensidad y suelen aparecer y desaparecer esporádicamente, haciendo q sea una enfermedad muy impredecible e incomprendida. ¿Cuál te resulta más limitante? #30DíasLupus #LupusAwarenessMonth

ICYMI, the National Lupus Advocacy Summit starts TOMORROW, and you're in luck because it's not too late to register: buff.ly/rV2uhQp

🎥 Did you miss our recent webinar on CAR Cell Therapy, T-Cell Engagers & Beyond? Catch up on the recording and hear from leading #lupus experts and a trial participant about the future of #lupusresearch and treatment breakthroughs. 💜 Watch now: buff.ly/3tU6fSW

We’re just 2 weeks away from the LRA New Jersey Walk with Us to Cure Lupus on Saturday, May 17 at MetLife Stadium, and it’s all happening during #LupusAwarenessMonth! 🙌👟 Let’s come together as one #lupuscommunity, to walk, support, and uplift each other. Enjoy a day of connection, including family-friendly fun like a DJ, Kids’ Zone, and bounce house. 👉 Register now as a team or individual and help raise funds for vital #lupusresearch: bit.ly/WALK25_NJ Together, we can take big steps toward a future free from #lupus. Because when it comes to making a difference, #ManyOneCan!

33% percent of people with lupus in the US are on work disability and the majority of them rely on a government health plan such as Medicare and Medicaid. The patient psychological and societal impacts are high—#LupusResearch to improve qol is the solution. #LupusAwarenessMonth

🎥 Don’t miss this! On May 6 at 8am PST, join Dr. Micah Yu for a Live Expert Session: "Lupus and Lifestyle Medicine" - streaming on our Facebook page. Learn how holistic care can empower #lupus patients. @myautoimmunemd #LupusLA #LupusAwarenessMonth

✅ Check my RED FLAGS for 'syndromic' #LUPUS 🚨🚩 Little details that should raise suspicion that what you see is MORE THAN LUPUS 👀 with a special focus on medication-induced lupus 💊 What would YOU add to this list? What are your personal red flags 🚩