Hereditary Angioedema - Privately Insured
OpenPrivately insured programs are designed for individuals with Group, COBRA, Individual, or Marketplace insurance, or are uninsured.
Am I likely eligible?
- Diagnosed with Hereditary Angioedema
- A U.S. resident receiving treatment in the U.S.
- Household income at or below 500% of the Federal Poverty Level Learn more about FPL (PDF, opens in a new tab)
- Uninsured
- Private Insurance
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
Private Insurance
- Copay
- Medical Expenses
- Premium
- Travel Expense
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 Association (HAEA)
Caregiver Resources
ARCH National Respite Network and Resource Center
National Alliance for Caregiving
Other Patient Assistance Organizations