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Hereditary Angioedema Financial Assistance Program

The Assistance Fund

UnknownUnder review·Mar 20, 2026

The Hereditary Angioedema Financial Assistance Program provides financial assistance for out-of-pocket costs including prescription drugs, health insurance premiums, therapy administration, and travel expenses (ground transportation, air travel, meals, hotel stay) to treatment centers or specialists, as well as genetic testing. It is open to U.S. citizens or permanent residents diagnosed with Hereditary Angioedema, who are prescribed an FDA-approved treatment, have prescription coverage, and meet financial eligibility criteria based on household income and size.

Covers
financial assistance
Enrollment cycle
unknown

Status source

Covered Diseases

Rare-disease support beyond financial help

This grant covers a rare condition. For specialists, clinical trials, and patient communities, our sister site UniteRare.org has in-depth pages: