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Lupus Association Profile
Lupus Association

@LADAOrg

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Following
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Statuses
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Improving access to care & quality of life by wielding the patient voice as a catalyst to advance advocacy, education, awareness & research efforts.

Verona, NY
Joined October 2016
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@LADAOrg
Lupus Association
2 months
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.
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@CAChronicCare
CA Chronic Care Coalition
6 days
TY, Governor @GavinNewsom, for signing #SB41 (@Scott_Wiener)!👏This bill protects patients & pharmacies by holding PBMs accountable. This is a huge win for everyone who cares about fair access to medicine and better healthcare. @SFAIDSFound @LALGBTCenter https://t.co/y5RabwpJU6
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gov.ca.gov
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@CAChronicCare
CA Chronic Care Coalition
4 days
🎉 Huge win! We are thrilled @CAgovernor has signed #SB41(@Scott_Wiener) into law! This imp bill is a big step toward lowering meds costs by regulating the practices of pharmacy benefit managers (PBMs) TY to everyone who stood with us to make this happen!  https://t.co/y5RabwpJU6
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@DFA2025
David F. Alfonso
4 hours
@Smith1988101 @PM_ViktorOrban It needs to end already and there will be no winners. It should have never started to begin with. At this point, Peace and compromise out ways picking sides. The senseless killing needs to end immediately. President Trump will get this conflict resolved! The EU has proven itself
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@LADAOrg
Lupus Association
10 days
3No one should pay twice for their meds! States must require cash payments count toward deductibles and OOP max. Thanks @mcubanfor leading the charge. Ohio can take action now! @Rob_McColley@BillReineke @SteveWilsonOH@LangforOhio @manningforOhiod#OHSB207 #AllCopaysCount
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@LADAOrg
Lupus Association
10 days
We’re calling on every senator: Do the right thing for Wisconsin families. Pass #SB203 today. @WisSenGOP @SenateDemsWI
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@Lupusreference
Laurent ARNAUD
13 days
✅ Happy to discuss with the #Rheumatology colleagues of Bulgaria that no dose of glucocorticoids is safe or innocent in #Lupus. In our recent nation-wide study in France (~30 000 patients with #SLE) we detected that even mean GC doses 1-5mg/day were associated with complications
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@CelsiusOfficial
CELSIUS Energy Drink
2 months
This is more than just four quarters. It’s every tailgate, every chant, every moment. It’s fuel that goes beyond the field. This is CELSIUS! LIVE. FIT. GO.
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@CaringForLupus
Caring For Lupus
13 days
Purple 💜 💪 Power Hispanic Heritage Month Every day, we see the strength Every week, we see Hope Every month, we need to make #Lupus visible #LupusAwareness is a continuous journey of compassion and support. Thank you Washington School #Lupuschat
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@LADAOrg
Lupus Association
22 days
•Dr. Maria Lopez exposes PBMs’ unregulated control, profiting off the backs of patients. @CAgovernor, #SB41 will bring accountability to California’s prescription drug market and ensure better access for underserved communities.
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capitolweekly.net
OPINION - To my fellow Californians, and Latino families: don’t be fooled. PBMs are not protecting you. They are profiting from you.
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@LADAOrg
Lupus Association
23 days
Thanks to action in @WaysandMeansGOP @WaysMeansCmte and @HouseCommerce @EnergyCommerce, the #MCEDAct is moving forward. The Senate must take the next step for patients everywhere. @gillibrandny @SenSchumer
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@LADAOrg
Lupus Association
1 month
We’ve reached the biggest milestone yet: the #MCEDAct has 2/3rds support in both chambers. With @WaysMeansCmte markup + @HouseCommerce hearing this week, Congress must finish the job. Thank you @RepTomSuozzi @RepNicole @RepTenney @RepAOC @RepLangworthy for leading the charge!
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@LADAOrg
Lupus Association
1 month
Join @obesityaction @OMAsocial on 9/23 to learn about the #obesity medicine landscape in 2025. Hear from patients, providers, and policy experts on the challenges facing people with obesity and get ready to advocate for change. Register now!
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us06web.zoom.us
Zoom is the leader in modern enterprise video communications, with an easy, reliable cloud platform for video and audio conferencing, chat, and webinars across mobile, desktop, and room systems. Zoom...
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@SLEuroSociety
SLEuro
1 month
The 7th SLEuro Advanced Workshop on SLE has started today in Tallinn (Estonia)! The 30 selected participants from all over the world and the Speakers are here with us for this interactive 2-day workshop about lupus ✅ #SLEuroWorkshop #lupus
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@Lupusreference
Laurent ARNAUD
1 month
✅ Very happy to be organizing the 7th @SLEuroSociety Advanced #Lupus #Workshop in Tallinn, Estonia, with the amazing Sandra Meisalu and our great #SLEeuro team! We will discuss complex #SLE situations with 30 lucky participants 👍 to improve care & knowledge.
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@LADAOrg
Lupus Association
1 month
States are losing billions in Medicaid savings due to 340B Program loopholes. In 2024 alone, states missed out on $2.3B in rebates, money that could support vulnerable patients.    @SenBillCassidy @SenMullin @SenAshleyMoody it's time to #Fix340B. https://t.co/7LIT0Fbrnq
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@LADAOrg
Lupus Association
1 month
Advocates are celebrating a major milestone: 290+ House and 60 Senate cosponsors for the #MCED Act. But cosponsors don’t save lives—passing the bill does. @SenSchumer @RepJeffries @SpeakerJohnson @SteveScalise. Congress must act now. Let’s get this done in 2025.
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@US_Pain
U.S. Pain Foundation
1 month
Childhood pain is real—and relentless. 53% say it never stops. 1 in 10 say nothing helps. This isn’t “growing pains.” It’s a care crisis. Read their stories: https://t.co/j22gaiwAwN #ThisIsPain #PediatricPain #PainAwarenessMonth #UnmaskingPain
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@LADAOrg
Lupus Association
1 month
Join @obesityaction @OMAsocial on 9/23 to learn about the #obesity medicine landscape in 2025. Hear from patients, providers, and policy experts on the challenges facing people with obesity and get ready to advocate for change. Register now!
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us06web.zoom.us
Zoom is the leader in modern enterprise video communications, with an easy, reliable cloud platform for video and audio conferencing, chat, and webinars across mobile, desktop, and room systems. Zoom...
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@LADAOrg
Lupus Association
1 month
Spot on from @mcuban. The “EHB loophole” is “PBM shenanigans” that the Trump Administration must address. @USDOL @SecretaryLCD we urge you to close the EHB loophole to protect patients from this harmful scheme. #AllCopaysCount
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@US_Pain
U.S. Pain Foundation
2 months
September is Pain Awareness Month—and we’re Unmasking Pain. Behind every chart is a life. Behind every stat, a story. Learn more: https://t.co/Y0ulMcqAde #ThisIsPain #UnmaskingPain #PainAwarenessMonth #USPainFoundation
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@FonziAI
Fonzi AI
1 month
Love wasting hours applying online just to hear nothing back? Yeah, engineers don’t either.
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@LADAOrg
Lupus Association
2 months
Thank you, @RepDavidValadao, for meeting with California advocates to discuss #PBMReform and the #MCEDAct. Your support of these patient-centered policies will help improve access for rare and chronic disease patients throughout the country.
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@GBecerraSD
Gerardo Becerra
2 months
@LADAOrg @Annezab @TurningStone @KathleenArntsen @SandiFrear @MasonicResearch @mkontari @LupusResearch @carrainc @RheumResearch @US_Pain @JessBateman02 Congratulations! So glad of the work you're doing and the generosity of your community. Let's find a Cure or Treatment for lupus in the near future. Gerardo from Lovely San Diego, CA 😍 .
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