Sandi Frear

[Lupus Europe @LupusEurope]

🏆 Congratulations to all recipients of the @eular_org Awards at #EULAR2026!

👏 A well-deserved recognition of outstanding contribution, commitment and leadership within the rheumatology community.

🦋 Inspiring to see this excellence celebrated today

[Lupus Association @LADAOrg]

High deductibles and hidden fees are driving up costs for healthcare and medications. #TXLege, please stand with patients and hold health insurers and PBMs accountable to improve affordability and access.  #PrioritizePatients #TX4HealthAccess @DanielAldersTX @RepJamesFrank

[Amanda G @LAlupusLady]

What a beautiful day on Capitol Hill.

#RheumAdvocacyConference26

[Trisha @TrishaReads8]

Cheering for @Jeanette_Lupus loudly! @LADAOrg @Lupus_Chat @SandiFrear @LupusNE @UMassLupus

[Lupus Association @LADAOrg]

We are grateful for #Lupus and #Arthritis Patient Experts like you sharing your story.

[Florida Medical Association @FloridaMedical]

On June 17 at noon ET, join us for a free live CME webinar that will help you navigate these difficult discussions with honesty and compassion. https://t.co/5tcq31ds8z

[Gus Bilirakis @RepGusBilirakis]

It was great catching up with Chairman Ken Hagan to discuss the challenges facing our region and the important work underway to position our community for continued growth and future success. I appreciate his leadership and commitment to strengthening our economy, improving infrastructure, and enhancing the quality of life for residents throughout the region.

[Fibromyalgia National Health Organization @FibroHealthOrg]

Migraine & Headache Awareness Month begins today! This month is a crucial opportunity to highlight the real and often invisible challenges faced by people living with headache disorders. Join us in the #PathToBetterDays campaign.

We've teamed up with other organizations to amplify awareness, and ensure that people living with headache diseases feel seen, supported, and understood.

Learn more here: https://t.co/NfwrhdO0UX

Thank you to @CoalitionCHAMP for bringing us all together. 💜

#MigraineAwareness
#HeadacheAwareness

[Laurent ARNAUD @Lupusreference]

✅ and this is the start of the #SLICC group meeting at #EULAR2026. Moving forward ⏩ the care of #lupus patients 👍 We have an incredible panel of international #SLE experts in the room today 🌍🌎🌏

[Amanda G @LAlupusLady]

Grateful to @LADAOrg for supporting me and the @ACRheum #RheumAdvocacyConf26 *amplifying the patient voice” #Rheum matters!

[Trisha @TrishaReads8]

Absolutely thrilled to see Mary McGowan join this important conversation! I am joining 💜 @LADAOrg @LupusMI @LupusNE @Lupus_Chat @CaringForLupus @UMassLupus

[Amanda G @LAlupusLady]

There is strength in numbers…
With @ACRheum & @ACRheumDC -collaborating matters.
@LADAOrg understands the importance of “amplifying the patient voice” together with @CSROAdvocacy @AWIRGROUP & others orgs.
#RheumAdvocacyConference26

[Lupus Association @LADAOrg]

We are honored to have you represent #LADAorg! #LupusWarrior 💜

[Lupus Association @LADAOrg]

Thank you @carrainc for being such a great pediatric research organization and partner! 💜

[Lupus Association @LADAOrg]

We need innovative #lupus research initiatives that include cross-sector collaborations, public-private partnerships and robust basic, clinical and translational projects that will enable scientists to investigate disease pathogenesis and physiology, identify biomarkers, design better clinical trial methodologies, prevent complications, develop precise diagnostic measures and safer, more effective treatments, and ultimately eradicate this devastating disease. #LupusAwarenessMonth #LupusAwareness

[Lupus Association @LADAOrg]

#Lupus is considered a disease of unmet medical need because of the lack of efficient diagnostic tools, effective therapies, and well-designed clinical trials. Only 1 day to go before the end of #LupusAwarenessMonth. Thank you to all who promoted #LupusAwareness 💜🦋!

[Amanda G @LAlupusLady]

Celebrating #LupusAwarenessMonth when you are going to be advocating with @ACRheum representing the “patient voice” on Capitol Hill is fun.

Grateful to @ACRheum and @LADAOrg for the honor to share my experiences living with Rheumatic Diseases with members of Congress.

[Lupus Association @LADAOrg]

We are proud to be one of @CVEEP’s 300 partners working together to share information on #vaccines and help protect communities from infectious diseases. We look forward to furthering this important work alongside CVEEP. Learn more: https://t.co/fqMFp1Hy1U @CVEEPSocial

[Lupus Association @LADAOrg]

#AB2009 passed the California Assembly floor with a unanimous vote! The bill will modernize outdated regulations on source plasma collection, helping increase access to plasma-derived medicines for patients. Thank you, @PhillipChenCA and @AsmSolache, for your leadership!

[Lupus Association @LADAOrg]

The annual per person with #lupus cost to employers, including medical care, work absence, and short-term disability, is higher than for other chronic diseases such as diabetes, chronic obstructive pulmonary disease, and heart disease. #LupusAwarenessMonth #LupusAwareness