The US Hereditary Angioedema Association (HAEA) is a non-profit organization dedicated to advocating for and conducting research on hereditary angioedema (HAE). They actively engage the HAE community through grassroots activities, providing personalized services to address the unique needs of individuals and their families affected by HAE. The HAEA works closely with expert physicians to improve diagnosis, knowledge, and treatment options for HAE, while supporting drug discovery research for future therapies.
The HAEA is committed to enhancing the quality of life for those with HAE by securing access to and reimbursement for modern HAE medicines. Their success in supporting clinical research has led to FDA-approved therapeutic options, and they continue to promote HAE education and awareness through a variety of initiatives. As a product and company neutral organization, the HAEA remains dedicated to advancing the field of HAE and supporting the development of innovative treatments for the condition.
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