🏆 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
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
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.
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
✅ 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 🌍🌎🌏
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 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 💜🦋!
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.
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
#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!
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