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 community’s quality of life through improving diagnosis and knowledge of the condition, and encourage an individualized approach to selecting an optimal treatment. The HAEA is product and company neutral, and continues to enthusiastically support drug discovery research aimed at the next generation of HAE therapies.
Our Mission:
To lead a nationwide advocacy movement that focuses on increasing HAE awareness and education, empowering access to suitable treatment, and fostering ground-breaking research that includes searching for a cure.
Our Vision:
Unrestricted access to therapy so people affected by HAE are unburdened by symptoms and able to experience life to the fullest.
Our Values:
To fulfill our community's highest priority needs with innovative programs, services, and activities that are delivered with an extraordinary level of empathy, kindness, and compassion.
Follow us on Social Media!
Facebook: @hereditaryangioedema
Twitter & Instagram: @us_haea
YouTube & Vimeo: @ushaea
Company Details
- Employees
- 31
- Founded
- -
- Address
- 10560 Main St, Fairfax,virginia 22030,united States
- Phone
- (866) 798-5598
- Industry
- Non-Profit Organizations
- Website
- haea.org
- Keywords
- hae, scientific research, advocacy, non profit, patient association, advance hae, patient support group, rare disease, hereditary angioedema, patient advocate.
- HQ
- Fairfax, Virginia
Hereditary Angioedema Association - Haea Questions
Hereditary Angioedema Association - Haea's helpline number is (866) 798-5598
Hereditary Angioedema Association - Haea's website is haea.org
Hereditary Angioedema Association - Haea's LinkedIn profile is https://www.linkedin.com/company/hereditary-angioedema-association-haea
Hereditary Angioedema Association - Haea has
31 employees.
View email and phone details for 31
employees at Hereditary Angioedema Association - Haea.
Hereditary Angioedema Association - Haea's industry is
Non-profit Organizations
Hereditary Angioedema Association - Haea's top competitors are
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Hae International (Haei),
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Hereditary Angioedema Association - Haea's categories are Non-profit Organizations
Hereditary Angioedema Association - Haea's founding year is 1999
