🔥The 9th Round of Easy Loan, Earn $40 Reward is in progress❗️ ⏰ Promotion Period: January 15th - Feburary 15th, 2025 👉 Register now and check more details at gate.io/campaigns/358

Tune in tonite WCVB Chronicle as Nicole Estaphan introduces many to the innovative wk of CAR-T cell therapy by Roberto Caricchio MD UMass Lupus as he forges this treatment path forward. Join his CAR-T cell session on 11/18 at #ACR24. #lupus #patient-champion #hope 💜🦋💁🏻‍♀️

✅ VERY FULL ROOM for the opening of Lupus Research Alliance's FORUM FOR DISCOVERY, where 200+ investigators will discuss top-level #Lupus research 👍 More than 259,000,000 US dollars has been funded so far as research grants. Check the website: lupusresearch.org

La deficiencia de vitamina D es común en pacientes con #Lupus. Debido a que son sensibles a la luz, evitan la exposición al sol ☀, lo que ayuda a crear vitamina D a través de la piel. Confirme con su médico cuál es un buen nivel de vitamina D y cómo puede lograrlo #LupusChat

While at #ACR2024 this weekend, we need to discuss how and *where* we will continue the social media portion of our advocacy and outreach in the #Rheum community. #LupusChat

In honor of #NationalFamilyCaregiversMonth, we spotlight Elizabeth SantaCruz’s story on how her teenage daughter Miah inspires her to be a passionate advocate for children and youth with lupus. She is a driving force in the #LupusABC Lupus Accelerating Advances Consortium, a

For Dr. Ashira Blazer, Assistant Professor of Rheumatology at the University of Maryland, #ACR24 means engaging in critical conversations about lupus care. With 10+ years treating lupus, she's excited about advancements and new options for patients. This is where the future

We are #ACR24 !!!! Ready 💜🦋 Miah will be a speaker at #ACR24 First pediatric Advocate to speak on "Cultural Humility for Pediatric Rheumatologists" 11/17 1-2pm 👈 Grateful for Lupus Association Kathleen Arntsen and Team for unwavering support #patientvoice #LADAorg #LupusChat

Awed by side by side patient poster presenters about the pediatric rheum experience. 膠サポKOSAPO JAPAN/Lupus/Rheumatic Disease/Vasculitis & Whitney Carter LaBar🎗👊, Chronically Awesome teach us pediatric patients need a voice in their own care #ACR24 #StrongerTogether 🦋

I finally met our #lupus research hero Laurent ARNAUD. Not only is he brilliant but he is always #patientfocused. We appreciate you Dr. Arnaud! Lupus Association #LupusChat Trisha Carly by Nature Anne Zablotowicz Caring For Lupus Tiffany ⁷ Kaamilah Gilyard Whitney Carter LaBar🎗👊, Chronically Awesome

Sooo Many people stopped by the Lupus Community booth #2200 this morning 🌞 ☀️ and engaged with patient-led organizations that are doing amazing community work #LupusChat #LADAorg #Lupus #PatientVoice

An emotional moment for our team today as Caring For Lupus & her daughter, Miah, a pediatric #lupus patient recount the obstacles in the journey for Miah’s care. Bravo to this mother/daughter team loved by all in our lupus community #ACR24 💜🦋

Congratulations 🎊 👏 Miah!!! History was made at #ACR24 💜👏🦋 First Pediatric Rheumatology Patient Speaker at American College of Rheumatology Primer Paciente De Reumatología Pediátrica en ACR24 Muchas Gracias a American College of Rheumatology CARRA Lupus Association por todo su apoyo #LupusChat #LADAorg #Lupus

It's Live!!! American College of Rheumatology Article ⤵️ Miah Makes History as the First Pediatric Rheumatology Patient Speaker at #ACR24 Thank you Kathleen Arntsen Lupus Association, American College of Rheumatology, CARRA for your unwavering support 💜🦋 #Lupus #LupusChat #LADAorg #Carepartners the-rheumatologist.org/article/system…

Caring For Lupus American College of Rheumatology Lupus Association CARRA #LupusChat @dawnmgibson.bsky.social @spooniechat.bsky.social UMass Lupus Lady Lupus Bubbsz 🥭💜🇧🇲🖤 Nuria #Lupus RarasNoInvisibles Anne Zablotowicz I encourage everyone to read the article and celebrate that after 20+ years of asking American College of Rheumatology to include more patient focused opportunities, this session highlights that we have finally arrived. Kudos to Miah and Elizabeth, it is a privilege to advocate with you. 💜💜💜🦋

This is an excellent service funding opportunity open to all UMass Chan Medical School students. Proposals are due Jan. 3: direc.to/m4K8 UMass Chan MD/PhD Program UMass Chan – Community & Government Relations Department of Medicine UMass Psychiatry and Behavioral Sciences UMass Chan Department of Neurology UMass Lupus UMass Chan Department of Dermatology Lamar Soutter Library at UMass Chan Medical School

Attention lupus patients and healthy volunteers! Please consider enrolling in our fully remote study of skin and blood. See photo below for study flyer and info (flyer attached)

Check out The Rheumatologist January 2025 issue that includes Miah’s presentation on #culturalhumility Thank you to American College of Rheumatology for including this groundbreaking session and Lupus Association Kathleen Arntsen CARRA & #LupusChat for their support #lupus the-rheumatologist.org/issue/january-…

Today, we reflect upon and honor the legacy of Martin Luther King, Jr. We are inspired by this meaningful quote and take to heart Dr. King’s words about doing good for others. #MondayMotivation #MLKday

In part 1 of this series, “Neuropsychiatric Lupus: 4 Questions with Dr. Meggan Mackay”, Dr. Mackay, rheumatologist and LRA-funded researcher, answers the question “What is Neuropsychiatric Lupus." Watch now to learn more! #InternationalQualityofLifeMonth

Comparative spatial transcriptomics of hair follicle-T cell interactions in mouse, dog and human reveals conserved drivers of primary ... biorxiv.org/cgi/content/sh… #biorxiv_immuno