HEREDITARY ANGIOEDEMA ASSOCIATION INC
The US HAEA is a non-profit advocacy and research organization serving people with HAE. #HereditaryAngioedema The US HAEA is a non-profit advocacy and research organization serving people with HAE. To lead a nationwide advocacy movement that focuses on increasing HAE awareness and education, empowering patient access to suitable treatment, and fostering ground-breaking research that includes searching for a cure.
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2005
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- HAEA 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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