Are you an early-career scientist or junior investigator committed to a career in rheumatology and #lupusresearch?
The LRA/ @RheumResearch Empowering Lupus Research Partnership is now accepting applications for funding that supports innovative, transformative #lupus research.
This is your opportunity to:
🟣 Investigate novel pathways in lupus biology
🟣 Drive breakthroughs in autoimmune disease
🟣 Bridge the gap from bench to bedside
Two award mechanisms are available:
~ Scientific Development Award - up to $225,000 over 2-3 years
~ Investigator Award - up to $500,000 over 3-4 years
LOI Due: July 1, 2026
Learn more and apply at https://t.co/Y45WIta1lL
The LRA is pleased to share the recipients of the 2026 Lupus Insight Prize: Gregory Barton, PhD, @UCBerkeley and Olivia Majer, PhD, @CincyChildrens for groundbreaking discoveries revealing how a key regulator of the immune sensor TLR7 keeps immune responses in check—and how changes in this pathway can contribute to lupus. Their work is opening new paths for more precise, targeted therapies.
The Prize will be awarded at @ACRheum #ACRConvergence2026 during the Lupus Research Alliance Lupus Insight Prize Lectureship. Save the date!
📅 November 10, 2026
🕛 3:30-4:30 PM ET
#LupusResearch #Lupus #LupusInsightPrize
💜 🦋 FUNDRAISING FRIDAY 🦋 💜
Donate any amount.
No gift is too small.
Every dollar helps @LupusOrg
fund research, education, advocacy, and the search for a cure for #lupus.
#ReneesButterflies 🦋
#WalkToEndLupusNow 👟
#CrushLupus
https://t.co/Xve4TqRlII
Have you ever wondered why there aren't treatments tailored to your specific #lupus symptoms? 💜 Your experience could help change that.
Join RAY®, the LFA's free, secure online registry, and help drive research breakthroughs: https://t.co/N8PkFMue3M
#LupusAwarenessMonth
Check out the Lupus Voices Council (LVC) Guide to Lupus Resources! 💜
Created by the #lupus community, this guide provides information, tools, and programs to strengthen clinical trial education and support people living with lupus.
The guide features information on:
✔ Community-driven projects
✔ Guidance on participating in clinical research
✔ Resources for people with lupus, caregivers, and advocates
Whether you’re a person living with lupus, caregiver, researcher, or advocate, this guide offers ways to learn, connect, and take action.
Explore the full guide here: https://t.co/BTCxPUNrER
#LupusABC #LupusResearch #LupusVoices
💜 Misdiagnosed for 19 years — multiple sclerosis, leukemia, and more, LFA Ambassador Nyobie always knew something was wrong.
She's sharing her #lupus journey so no one else has to wait long for answers. Read her story in @People: https://t.co/MPXDELQmac
#LupusAwarenessMonth
💜 Getting the most out of your doctor visits when you have #lupus isn't always easy — but our free SELF app was built to help. Hear from lupus warriors using SELF to communicate with their care team.
Download the SELF app today: https://t.co/7eJpofPhHw
#LupusAwarenessMonth
Our #KnowLupus Quiz is live—are you up for the challenge? It’s time to test what you REALLY KNOW about #lupus.
💜 Take the quiz, post your score, tag us, and we'll reshare! Let’s #MakeLupusVisible!
Play now: https://t.co/MVL6Yt0KwE
May is #LupusAwarenessMonth 💜
Although Lupus is a chronic autoimmune disease, it is also an invisible illness. This May, Marlene’s Kaleidoscope is committed to spreading awareness & support for the lupus community. Together, we can make a change! 💜🦋
#LupusWarriors#MK4LUPUS