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Pompe

Up to $10,000 available in assistance for Private/Uninsured & Public

Check Eligibility & Apply for Pompe (opens in a new tab)

Pompe - Privately Insured

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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?

$8,500 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

According to the U.S. National Library of Medicine, Pompe disease is an inherited disorder caused by the buildup of a complex sugar called glycogen in the body’s cells. The accumulation of glycogen in certain organs and tissues, especially muscles, impairs their ability to function normally. The classic form of infantile-onset Pompe disease begins within a few months of birth. The non-classic form of infantile-onset Pompe disease usually appears by age one and the late-onset type of Pompe disease may not become apparent until later in childhood, adolescence, or adulthood. 

Pompe - Publicly Insured

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Check Eligibility & Apply for Pompe - 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?

$10,000 total assistance available, shared across all types below

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

According to the U.S. National Library of Medicine, Pompe disease is an inherited disorder caused by the buildup of a complex sugar called glycogen in the body’s cells. The accumulation of glycogen in certain organs and tissues, especially muscles, impairs their ability to function normally. The classic form of infantile-onset Pompe disease begins within a few months of birth. The non-classic form of infantile-onset Pompe disease usually appears by age one and the late-onset type of Pompe disease may not become apparent until later in childhood, adolescence, or adulthood. 

Diagnosis codes

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

  • E74.02 Pompe disease

Covered medications

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

  • Alglucosidase Alfa
  • Avalglucosidase Alfa-ngpt
  • Cipaglucosidase Alfa-atga
  • Lumizyme
  • Nexviazyme
  • Opfolda
  • Pombiliti
  • migLUstat (GAA Deficiency)

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.

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)