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🎉 What an unforgettable experience at the 2025 US HAEA National Summit in Baltimore, MD! 💜 The HAEA Community came together to connect, learn, and inspire.� 🌟 Together, we are Embracing a Brighter Future! #TB #HAEACommunity #2025HAEASummit #EmbracingABrighterFuture #HereditaryAngioedema #HAE | Hereditary Angioedema Association - HAEA
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🔴 📣 Watch this month’s new US HAEA Treatment Education Series Webinar: “Living with HAE: Insights and the HAE Community Survey.” Join us for an inspiring conversation with Dr. William Lumry and Kim, a person with HAE. Together, they’ll share results from the recent HAE Community Survey and provide real-world insights into what it means to live with hereditary angioedema. #HAEA #HAEAwareness #HAEATreatmentSeries #HereditaryAngioedema #HAECommunity | Hereditary Angioedema Association - HAEA
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Join us at the HAEA Round Table, where members of our community discuss how they have dealt with the unique challenges of HAE. This event will feature people with HAE and will showcase their answers to questions related to Factor 12 and HAE. Thank you to this episode's sponsor: CSL Behring. | Hereditary Angioedema Association - HAEA
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