HEREDITARY ANGIOEDEMA ASSOCIATION INC
- HAEA
251852548
2005
Fairfax, VA 22030 USA
haea.org
US_HAEA
hereditaryangioedema
2200421
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News
Did you know? … There are more than 133 million Americans diagnosed with at least one chronic illness. 💭 Join the HAEA on July 10th as we celebrate Chronic Disease Day. This year, we’re asking you to advocate for change by: Joining our HAEA Grassroots Advocacy Network using the link here: https://bit.ly/3IQMFFU Registering for the 2025 HAEA Virtual Capitol Hill Day taking place on September 25th, 2025! Registration Link: https://bit.ly/43DzOkK #ChronicDiseaseDay2025 #DidYouKnow #HAEAdvocate (fb)
🎉 We have an exciting Youth Leadership Program planned for our 2025 US HAEA National Summit! Here’s a sneak peek into what our youth members will be doing at the 2025 Summit! Do you have any guesses about what fun activity we have planned? 👀 What are you most excited for? #HAEASummit2025 #HAECommunity #HAEAwareness #beyondhae #HereditaryAngioedema (fb)
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About the organization
- 513, E60, P99, H90 -
To lead a nationwide advocacy movement that focuses on increasing HAE awareness and education empowering access to suitable treatment and fostering groundbreaking research that includes searching for a cure. Unrestricted access to therapy so people affected by HAE are unburdened by symptoms and able to experience life to the fullest. To fulfill our communitys highest priority needs with innovative programs services and activities that are delivered with an extraordinary level of empathy kindness and compassion. TAKE ACTION Your contribution helps fund our many programs and resources for people living with HAE and their loved ones Join our efforts to maintain a strong political advocacy presence on Capitol Hill Get involved and help serve our community Participate in one of our many ongoing initiatives or create your own.
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