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Hereditary Angioedema

Up to $9,500 available in assistance for Private/Uninsured & Public

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Hereditary Angioedema - Privately Insured

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Check Eligibility & Apply for Hereditary Angioedema - Privately Insured (opens in a new tab)

Privately insured programs are designed for individuals with Group, COBRA, Individual, or Marketplace insurance, or are uninsured.

Am I likely eligible?

This is a guide, not a decision. Checking your eligibility takes a few questions and gives you an answer.

What assistance is available?

$9,500 total assistance available, shared across all types below

Uninsured

  • Copay
  • Medical Expenses
  • Travel Expense up to $500

Private Insurance

  • Copay
  • Medical Expenses
  • Premium
  • Travel Expense up to $500

Hereditary Angioedema (HAE) is a very rare and potentially life-threatening genetic condition.  It is caused by a low level or improper function of a protein called C1 inhibitor. HAE occurs in about 1 in 10,000 to 1 in 50,000 people. Symptoms may include swelling in various parts of the body including hands, feet, face, intestinal tract, limbs, and airway (throat). 

Resources

These organizations offer information and support for this condition. They are independent of Accessia Health, and may not currently have assistance available for this program.

Hereditary Angioedema - Publicly Insured

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Check Eligibility & Apply for Hereditary Angioedema - Publicly Insured (opens in a new tab)

Programs for those with public or federally sponsored insurance include all forms of Medicare, Medicaid, Tricare, or Veterans.

Am I likely eligible?

This is a guide, not a decision. Checking your eligibility takes a few questions and gives you an answer.

What assistance is available?

$7,500 total assistance available, shared across all types below

  • Copay
  • Medical Expenses
  • Premium
  • Travel Expense up to $500

Hereditary Angioedema (HAE) is a very rare and potentially life-threatening genetic condition.  It is caused by a low level or improper function of a protein called C1 inhibitor. HAE occurs in about 1 in 10,000 to 1 in 50,000 people. Symptoms may include swelling in various parts of the body including hands, feet, face, intestinal tract, limbs, and airway (throat). 

Resources

These organizations offer information and support for this condition. They are independent of Accessia Health, and may not currently have assistance available for this program.

Diagnosis codes

Your provider uses one of these codes when confirming your diagnosis. You do not need to know your code to apply.

  • D84.1 Defects in the complement system
  • T78.4 Other and unspecified allergy
  • T78.40 Allergy, unspecified

Covered medications

22 medications are covered by this program. Assistance is not limited to medication costs.

  • Andembry
  • Berinert
  • Berotralstat HCl
  • C1 Esterase Inhibitor (Human)
  • C1 Esterase Inhibitor (Recomb)
  • Cinryze
  • Danazol
  • Dawnzera
  • Donidalorsen Sodium
  • Ecallantide
  • Ekterly
  • Firazyr
  • Garadacimab-gxii
  • Haegarda
  • Icatibant Acetate
  • Kalbitor
  • Lanadelumab-flyo
  • Orladeyo
  • Ruconest
  • Sajazir
  • Sebetralstat
  • Takhzyro

Ready to find out if you qualify?

Checking your eligibility takes a few questions and gives you an answer. If this program is at capacity you can join the waitlist and we will contact you when it reopens.

Check Eligibility & Apply (opens in a new tab)