May 16th is hae day :-)! The HAEA invites YOU to TAKE ACTION FOR HAE throughout the entire month of May! Order a newly updated HAE ER Toolkit and receive a FREE limited edition TAKE ACTION FOR HAE t-shirt! Order yours today, and share it with your local first responders, medical emergency rooms, school nurses, dentist, family physician, coaches, and anyone you would like to learn more about HAE. Order your ER Toolkit here: https://fundraise.haea.org/2021-hae-day #haeday #HereditaryAngioedema #HA

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🔴 📣Watch this month’s new US HAEA Treatment Education Series Webinar: The TAKHZYROⓇ Experience and YOUR Family. Join Dr. William Lumry and SynToia, a Patient Ambassador, for an insightful discussion on the real-world experience of using TAKHZYROⓇ. This session will combine medical expertise with a personal perspective, offering practical information for patients and families navigating treatment options. #HAEA #HAEAwareness #HAEATreatmentSeries | Hereditary Angioedema Association - HAEA

🔴📣Watch this month’s new US HAEA Treatment Education Series Webinar: ADX-324 (siRNA): Advancing HAE Care; Next Generation of Treatments. Join us for an engaging discussion featuring Dr. Marc Riedl and Dr. Masako Murai, Vice President of Clinical Development at ADARx Pharmaceuticals, who will provide an overview of ADX-324 (siRNA) and discuss how this investigational next-generation therapy may advance care for people living with hereditary angioedema (HAE). #HAEA #HAEAwareness #HAEATreatmentSe

This HAE Speaks episode re-visits the HAEA National Summit session from HAE Expert and US HAEA Medical Advisory Board Member, Dr. Marc Riedl, as he offers a crucial look at the future of HAE care. 👏 The discussion focuses on the rapidly advancing treatment landscape, covering the latest novel therapies in development, and how these advances aim to improve treatment efficacy, convenience, and quality of life for the HAE community. 🎙️Listen to full episode HERE:🎙️ https://open.spotify.com/episo