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Hereditary Angioedema Financial Assistance Program

The Assistance Fund

OpenVerified·Mar 20, 2026

The Hereditary Angioedema Financial Assistance Program by The Assistance Fund provides financial assistance for out-of-pocket medical costs related to Hereditary Angioedema, including prescription drug copays, deductibles, coinsurance, health insurance premiums, therapy administration, genetic testing, and travel expenses (ground transportation, air travel, meals, hotel stay) to treatment centers or physicians. To qualify, patients must be U.S. citizens or permanent residents diagnosed with Hereditary Angioedema, 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

Eligibility

Applicants must be U.S. citizens or permanent residents diagnosed with Hereditary Angioedema and prescribed an FDA-approved treatment with existing prescription coverage. Eligibility also requires meeting financial criteria based on household income and size, though specific thresholds are not listed.

Status source

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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: