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Eosinophilic Granulomatosis with Polyangiitis (EGPA)

Young woman doctor listens to older woman patient's chest with a stethoscope. Young woman doctor listens to older woman patient's chest with a stethoscope.

Eosinophilic granulomatosis with polyangiitis (EGPA) is a rare form of vasculitis, meaning it causes inflammation in small and medium sized blood vessels, which can result in damage to organs throughout the body. In most patients, blood vessels in the lungs are affected, causing breathing and lung issues.

Understanding Your Lung Health: EGPA

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Dr. Mora in a lab coat explains EGPA.

Learn About EPGA

Learn more about this rare condition and what role the immune system plays.

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Symptoms and Diagnosis of EGPA

The symptoms of EGPA vary widely from person to person and can also range from mild to severe. Diagnosis of EGPA is often delayed because the disease is so rare it isn’t top of mind for healthcare providers.

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Treating and Managing EGPA

Treatment for EGPA can vary depending on the presentation of symptoms. Work with a provider who has experience treating EGPA to agree upon a treatment plan that works for you.

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Newly Diagnosed with Eosinophilic Granulomatosis with Polyangiitis (EGPA)

EGPA is a rare disease previously known as Churg-Strauss syndrome. In most patients it affects your lungs, but it can also affect other organs in your body. It is important to know what steps to take when you have been diagnosed.

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Did you know asthma can mask rare lung diseases like aPAP and EGPA?

Learn the symptoms and ways to advocate for your lung health.
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