Hereditary Angioedema (HAE) Awareness Day took place on the 16th of May

CSL is delighted to announce the appointment of Mary Oates as the new Chief Operating Officer. In this pivotal role, Mary will lead CSL’s enterprise Operations organization, encompassing manufacturing, quality, supply chain, technical operations, and network strategy. Mary brings a wealth of leadership expertise spanning more than 25 years in the biopharmaceutical industry. We extend our warmest welcome to Mary and look forward to the impact she will make. Click here to learn more about our leadership: https://bit.ly/3SeDdkF #CSL #Leadership #DrivenByOurPromise

On #HAEDay , we’re proud to unite with the hereditary angioedema \(#HAE \) community in raising awareness of this rare and debilitating genetic disease. Our commitment to advancing treatments for HAE remains steadfast. Our ultimate goal is to improve the quality of life for people like Arianna, who courageously navigate the day-to-day fear of experiencing a painful and potentially life-threatening swelling attack. Together, we can drive innovation and work towards a future where those affected by HAE can live without fear of attacks. Read more of Arianna’s experience with HAE and her hopes for the future of HAE treatment: https://lnkd.in/eT9XUEjU #CSL

🌎 Today, on International Vasculitis Day \(IVD\), we are happy to celebrate a major step forward in raising global awareness for vasculitis: the introduction of the first-ever official logo for IVD. This new visual identity, developed by Vasculitis International and chosen by the global patient community, marks a significant milestone in amplifying the visibility of this rare and complex group of diseases — and we are proud to have supported this important initiative. See the logo here https://lnkd.in/eVus29X3 At CSL, we understand that living with ANCA-Associated Vasculitis \(AAV\), a type of rare and severe vasculitis, is about far more than managing a medical condition. It’s about navigating a journey marked by uncertainty and challenges — many of which remain invisible. That’s why our commitment goes beyond developing treatments. We believe true innovation is only possible when we walk alongside patients and truly listen to their voices. Through initiatives like the Vasculitis Together, and hand-in-hand with patients, advocates, and partners worldwide, we are driving forward progress — because behind every innovation, there is a human story that matters. On this important day, we invite you to hear directly from AAV patients Catherine and Shanali — voices that inspire all of us in CSL to push forward. Today, we reaffirm our promise: We see you. We hear you. We stand with you. Learn more on AAV https://lnkd.in/eM5Tn-8C #VasculitisDay #AAVAwareness #HolisticCare #LifeWithAAV #IVD2025

Today, on IgAN Awareness Day, we stand with everyone affected by IgA nephropathy — a rare, chronic kidney disease that can ultimately lead to kidney failure. Also known as Berger’s disease, IgAN impacts approximately 2.5 in 100,000 people per year worldwide. Its early symptoms are often subtle or absent, which means many live with the condition for years before receiving a diagnosis. While it can affect anyone, IgAN is most commonly diagnosed in young adults between their teens and late 30s — often just as they're planning their futures. At CSL, we are deeply committed to making a meaningful difference for people living with IgAN. We are proud our innovative treatment for IgAN has been converted from conditional to standard marketing approval in the European Union — a major step forward that will offer new hope to more patients and their families across Europe. But innovation doesn’t stop at treatment. Through initiatives like My Kidney House https://bit.ly/3GSDkjv, we provide patients and caregivers with reliable, easy-to-understand resources to help them better navigate their healthcare journey. Awareness matters. Early diagnosis matters. Innovation matters. And at CSL, we’ll continue to advance science and amplify support — because every person living with IgAN deserves to be seen, heard, and helped. Learn more about how IgAN impacts the kidneys by watching our short explainer video here https://bit.ly/44C34ug? #IgANAwarenessDay #KidneyHealth #KidneyDisease #MyKidneyHouse #CSL

Tomorrow’s medical breakthroughs start today. At CSL, research is about making discoveries that lead to impact. Join a team dedicated to shaping the future of medicine. #PromisingFutures #CSL Explore opportunities: https://bit.ly/44w86bC

On International Nurses Day, we recognize the dedication, compassion and expertise of nurses around the world. Their role in patient care is invaluable, especially for those managing rare and serious conditions. At CSL, we see firsthand how nurses provide critical support to patients, from guiding treatment journeys to advocating for better health care access. Today, we thank them for their tireless commitment to improving lives. #InternationalNursesDay

Living with ANCA-Associated Vasculitis \(AAV\) changes everything — even when you already know the disease inside out. Shanali, a rheumatologist and an AAV patient herself, shares her powerful story of resilience. For two years, she pushed forward, balancing her medical career and the daily weight of symptoms. But AAV eventually forced her to pause — not just her work, but her life as she knew it. Letting go of control became her turning point. Instead of fighting her symptoms every moment, she focused on what she could create. Through art, she found a way to transform invisible struggles into colors, shapes, and new energy. Today, Shanali reminds us that resilience isn't about never falling — it's about finding new ways to stand back up. Whether through painting, music, cooking, or gardening, having a creative outlet can be a lifeline. Hear her full story here https://bit.ly/4jRkPdW 💙 Thank you, Shanali, for showing what true strength looks like — and for inspiring others to find beauty even in the hardest days. What does resilience mean to you? Share your thoughts with us in the comments below. 👇 #VasculitisDay #AAVAwareness #PatientsVoices #Resilience #LifeWithAAV

Did you know? The rare condition hereditary angioedema \(HAE\) causes unpredictable, potentially fatal swelling episodes. Watch this one-minute video to understand what 17-year-old Jack experienced when his throat began to swell. CSL is proud to be an innovator in treatments for HAE and we celebrate #HAEDay \(May 16\) with the entire community of patients and patient families.