Hereditary Angioedema Association - HAEA

The HAEA is an advocacy and research organization committed to actively engaging our community in a wide variety of grassroots activities that promote HAE education and awareness. We provide personalized services to address the unique needs of people with HAE and their families, which includes helping them secure access to and reimbursement for modern HAE medicines. Our great success in supporting clinical research has resulted in a variety of FDA-approved therapeutic options. We work closely with expert physicians to continuously upgrade our communitys quality of life through improving diagnosis and knowledge of the condition, and encourage an individualized approach to...

Hae,scientific research,advocacy,non profit,patient association,advance hae,patient support group,rare disease,hereditary angioedema,and patient advocate

Hereditary angioedema association - haea operates in the Non-profit organizations industry.

Hereditary angioedema association - haea's revenue is 11m - 100m

Hereditary angioedema association - haea has 11 - 50 employees.