#LupusResearch
For me who depends on #SocialSecurity #SharingIsCaring, who can please donate.
💖💖💖
#LupusResearch in the USA will also help me as German, or any other person from any other country who has #SLE.
German experts´re far behind at it anyway... We only have the #RheumaLeague.
www.lupus.org
@lupus.org
October 25, 2026 at 8:15 AM
Lupus Science & Medicine, our open-access journal, has achieved an updated 2025 Journal Impact Factor of 4.3, up from 4.2! This marks the highest current Impact Factor of any #lupus-specific journal.

Explore the latest #lupusresearch: buff.ly/xi5qaLT
October 20, 2026 at 9:37 PM
Have you heard of Inside #Lupus Research? It's your one-stop location for learning about the most important #lupusresearch news that matters to you.

Stay on top of the latest, check out the current headlines and subscribe to get them straight to your email: buff.ly/NEpPVTI
September 15, 2026 at 4:03 PM
Canberra photographer Tyren donated 100% of the proceeds from two exhibition prints to
Garvan, in support of his partner Monique, who lives with lupus. Thank you, Tyren.

🔗Learn more about Garvan's lupus research: https://ow.ly/xxHJ50ZC7Gy

#LupusResearch #CommunityFundraising #LupusAwareness
August 21, 2026 at 1:30 AM
bsky.app/profile/mari...
Who´s not on #SocialSecurity like me, who can afford it, please donate to support #LupusResearch, for me #SharingIsCaring.
Results from the USA will also be published in Europe sooner or later.
💖💖💖👍👍👍
@lupus.org
The #AnnualReport from the @lupus.org is online.
I´m a longtime #SLE survivor since 1992 from SW Germany, diagnosed in 08/2002, who subscribed for their newsletter since we only have the Rheuma League in Germany, for all kinds of rheumatic diseases, but no Lupus org.
www.lupus.org/about-us/ann...
August 20, 2026 at 9:01 AM
August is National Make-A-Will Month!
If you have anything to pass on, which I don´t, you can support #LupusResearch.
💖💖💖
partner.freewill.com/lfalegacygiv...
@lupus.org
August 12, 2026 at 10:02 AM
Reeve Bright Named the Lupus Foundation of America’s Inaugural Men on a Mission™ Top Fundraiser.
Good job. The money helps #LupusResearch a lot.
💖💖💖
www.lupus.org/news/reeve-b...
@lupus.org
July 15, 2026 at 9:52 AM
#SharingIsCaring, who can please donate to support #LupusResearch, I have #SLE myself and am on #SocialSecurity, so I can only post on X & Bluesky.
Longtime survivor here since 1992, my advice: Never give up, believe in yourself.
💖💖💖
lupusuk.org.uk/make-a-donat...
@lupusuk.bsky.social
December 19, 2025 at 1:58 PM
It was a great morning to walk to cure Lupus at @MetLifeStadium with the #ShiaraShow and hundreds of people supporting research to find a cure for Lupus #LupusWarrior #LupusResearch
May 17, 2025 at 8:13 PM
#LADAorg is honored to sponsor a table at the LRA Gala to recognize people with #lupus for their grace, dignity and courage while supporting #lupusresearch.
@lupuschat.bsky.social @annezab.bsky.social @caringforlupus.bsky.social @masonicresearch.bsky.social @lupusresearch.bsky.social
November 25, 2025 at 8:16 AM
We are thrilled to share that our 25th Annual #Lupus Charity Golf Classic raised over $205,000 last week at Shenendoah Golf Course and we donated another $539,724 for #LupusResearch. Thank you to our volunteers, sponsors, golfers and #TurningStone sales, catering and golf staff.
August 23, 2025 at 3:41 PM
33% percent of people with lupus in the US are on work disability and the majority of them rely on a gov’t health plan such as Medicare and Medicaid. The patient psychological and societal impacts are high—#LupusResearch to improve qol is the solution. #LupusAwarenessMonth @lupuschat.bsky.social
May 4, 2025 at 8:15 AM
We are thrilled to support the @LupusResearch Breakingthrough Gala this year by sponsoring a table for passionate #LupusWarriors, #Carepartners, advocates and researchers who amplify the #PatientVoice. #LADAorg @caringforlupus.bsky.social @infusioncenter.bsky.social @lupuschat.bsky.social
December 9, 2024 at 4:34 PM
E.M.E.R.G.E. has been used in multiple trials with leading pharmaceuticals, schedule a demo and see what it can do for your study! E.M.E.R.G.E. is waiting to make your life easier! #ResearchWeek #crisalisllc #emergedatacollection #acrconvergence #Lupus #LupusResearch
www.crisalisllc.com/contact
Get in Touch with CRISALIS | Innovative Research Software for Clinical Trials
Have questions or need a custom software solution? Contact CRISALIS today to discuss your research needs or schedule a demo for one of our products.
www.crisalisllc.com
July 26, 2025 at 12:22 AM
E.M.E.R.G.E. is designed in collaboration with leading clinical trial experts. It includes a query messaging system with automated edit checks, in-depth manuals, and an in-house support team. #ResearchWeek #crisalisllc #lfapoint #emergedatacollection #acrconvergence #MedSky #Lupus #LupusResearch
July 26, 2025 at 12:22 AM
E.M.E.R.G.E. has been audited and validated to ensure complete regulatory compliance! With our 21 CFR Part 11 E-signatures module, HIPAA compliant data entry, and strong documentation practices, this system can help your trial succeed. #crisalisllc #acrconvergence #Lupus #LupusResearch #ResearchWeek
July 26, 2025 at 12:22 AM
Ensure data accuracy with a comprehensive audit trail, unique edit-check technology, and automated & validated assessment scoring. #ResearchWeek #crisalisllc #lfapoint #emergedatacollection #clinros #proforms #acrconvergence #MedSky #Lupus #LupusResearch
July 26, 2025 at 12:22 AM
Our Electronic Medical Evaluation & Research Gathering Engine (E.M.E.R.G.E.) can be adapted for use in different types of disease research that use ClinRos & PROs. #ResearchWeek #crisalisllc #lfapoint #emergedatacollection #clinros #proforms #acrconvergence #MedSky #Lupus #LupusResearch
July 26, 2025 at 12:22 AM
Big win for lupus research! 🦠🔍 Linking EBV to lupus is groundbreaking. Kudos to Stanford for backing EBVio Inc—innovation like this can change lives! 🚀 #Biotech #LupusResearch #EBVio
November 17, 2025 at 1:03 PM
Huge win for lupus research! 🧬 Linking EBV to pathogenesis opens new doors for treatment. Kudos to Stanford & EBVio Inc for pushing boundaries! 🚀 #Innovation #Healthcare #LupusResearch
November 14, 2025 at 9:01 PM
So honored to have been highlighted by the LRA @LupusResearch for my contributions to lupus care and research! Check out the feature: https://www.lupusresearch.org/lupus-gains-a-strong-black-advocate-in-physician-researcher-dr-ashira-blazer/
November 22, 2024 at 3:22 PM
The best way to spend a beautiful Saturday? Walking to end #lupus with team @HSpecialSurgery benefitting the @LupusResearch 💜💜🦄🦄
November 22, 2024 at 11:22 AM
Ending an excellent @LupusResearch meeting with a dinner full of generations of Black Women in rheumatology! Yes please! @DrBB11651372 @AWIRGROUP #WomenInSTEM #RheumTwitter
November 22, 2024 at 11:06 AM