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Hereditary Angioedema Financial Assistance Program

The Assistance Fund

OpenVerified·Mar 20, 2026

The Hereditary Angioedema Financial Assistance Program provides financial assistance for out-of-pocket costs including prescription drug copays, deductibles, coinsurance, health insurance premiums, therapy administration costs, and travel expenses (ground, air, meals, hotel) to treatment centers or prescribing physicians. To qualify, patients must be U.S. citizens or permanent residents, diagnosed with Hereditary Angioedema, prescribed an FDA-approved treatment with prescription coverage, and meet financial eligibility criteria based on household income and size.

Covers
financial assistance
Enrollment cycle
unknown

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: