🔬 #NewsFromTheLab Alert! 📣 Discover the LuGENE® Blood Test on April 16th, 4pm PST - a game-changer in predicting lupus flares & drug targets. Hear from Dr. Grammer, Dr. Lipsky & celebrity rheumatologist Dr. Wallace. Tap the live video on 4/16 at 4pm PST on Facebook to join!

✍🏻Completează sondajul.

🔊Împărtășește cu comunitatea ta.

👨🏼⚕Dacă ești un profesionist în sănătate și tratezi pacienți cu lupus în Europa, am aprecia foarte mult dacă i-ai informa pe pacienții tăi.

s.surveylegend.com/-NrUOqKxZuU6V6…

Un 10 de Mayo lleno de actividades❗️
Aprovecha la oportunidad ➡️ Ya puedes agendar este evento de las compañeras de Asociación Catalana Lupus E.G. con el Dr. gerard espinosa 🙌
Envía tu pregunta antes del 21 de Abril en el siguiente enlace y será contestada ⬇️⬇️⬇️ docs.google.com/forms/d/e/1FAI…

In celebration of #Lupus Awareness Month, the HSS Department of Social Work Programs, in collaboration with the Lupus & APS Center of Excellence & Department of Nursing, will be hosting free virtual & in person educational programs. To register, visit brnw.ch/21wIE9K.

NOW LIVE! Watch S3EP13 of the #YourStoryOurFight podcast to hear from Artist, Mother & Lupus Advocate, Donna Jordan! Tap to watch this inspiring Full Episode on #LupusLA ’s YouTube: youtube.com/watch?v=8ESTkk…

✅ En route to #PANLAR2024 🌎
I have 5 talks there, and many MORE amazing friends & colleagues 👍 I will talk about:
- Hot controversies in #SLE 🔥
- Can we stop #HCQ in #Lupus ?
- New EULAR guidelines for #SLE
- Management of refractory #Lupus
- Relapsing #polychondritis 👂

For #LivingWith , I spoke to Tiffany ⁷ about the years before she got a lupus diagnosis, and how she’s been able to build an international online patient community since: statnews.com/2024/04/09/lup…

✅ I'm very happy to announce that after 1 year of intense labor ⏱️ our #RECOMMENDATIONS 🧑‍🎓 for PHYSICAL ACTIVITY & EXERCISE 🏃🏋️⛹️🤸 for persons living with #LUPUS 🦋 are now ONLINE! For FREE, for all 👍
DIRECT DOWNLOAD LINK 📥rmdopen.bmj.com/content/rmdope…

🇵🇹 Viver com Lúpus em 2024 já está disponível em Português!

✍️ Responda à pesquisa, compartilhe com sua comunidade e ajude-nos a conhecer as diferentes facetas do lúpus 🦋

buff.ly/4cKKy4s

🦋El diagnóstico del #lupus neuropsiquiátrico es un reto ya q las manifestaciones neuropsiquiátricas no siempre tienen su origen en el #LES .

Otras posibles causas son:

- Infecciones
- Efecto adverso d medicación
- Anticuerpos antifosfolípido

El tratamiento dependerá d la causa

En el #DíaMundialDeLaSalud como Ministerio de Salud nos adherimos, y trabajamos juntas y juntos por el lema que la OPS/OMS promueve este 2024 #MiSaludMiDerecho .

Saludamos y agradecemos el trabajo de todas las funcionarias y funcionarios de la red asistencial. que a diario…

💙 Check out this inspiring conversation between two teens with rare autoimmune diseases. Hear how Spencer's unexpected journey taught him how to embrace life with new challenges. #autoimmune #raredisease #patientengagement
🎧 Listen here podcasts.apple.com/us/podcast/the…

🔥FREE CME:

😍Learn about how #Sjogrens affects major organs in a large percentage of patients; how to diagnose; how to treat:

👉 CLICK: pri-med.com/online-cme-ce/…

Brought to you by Sjögren's Foundation and Pri-Med CME

🦋 Dermatología juega un papel clave en el manejo del #lupus .

Aunque las manifestaciones cutáneas del #LES no suelen ser graves, sí q pueden afectar profundamente a la salud emocional y mental del paciente.

🥰 ¡Gracias a Fundación Piel Sana de la AEDV de Academia Española de Dermatología y Venereología por contar con nosotros!

🌍The right to health is a basic human right.

🏥Everyone must have access to the health services they need when & where they need them without 💶 hardship.

🚨30% of the global population is not able to access essential health services

#MyHealthMyRight #WorldHealthDay #WHD2024

Agradecer invitación y atención de Fundación Piel Sana de la AEDV en la I Jornada de la Fundación de Piel Sana de la @aedv en Madrid, donde confluyen especialistas y entidades de pacientes, charlas formativas, #ActividadesEducativas #SaludYpiel #PielyNiños #EtapasDeLaPiel
Con ganas de repetir❗️

It’s #NationalVolunteerMonth ! We are so grateful for our community and every individual that volunteers with the LRA. Your support is extremely valued and makes a difference. Thank you! 💜

No individual can do it alone, but together #ManyOneCan !

The Sjögren's Foundation began with story sharing and now, 40 years later, they are still working to keep the spirit of national awareness alive with their #ThisIsSjögrens campaign, highlighting individuals living with #Sjögren ’s every day in April. Lupus Association #LupusChat Caring For Lupus

Today, I participated in a fireside chat at an offsite for a team of immunology & rare disease researchers in Cambridge, MA. Still walking on clouds with the immense interest in this patient’s long journey living with #lupus & their commitment to push forward with research. 💜💁🏻‍♀️

We're wishing everyone a Happy Easter Sunday. May today be filled with lots of laughter, joy, love, and peace. 💜💙💛💚❤

~The #LupusChat Team