Living with EGPA: a patient’s view

1 Aug 2025

Mary McCarthy was diagnosed with eosinophilic granulomatosis with polyangiitis (EGPA) over 30 years ago. Today, she is a passionate advocate for EGPA patients, through her work with the EGPA/Churg Strauss International Friends support group.

Mary shares her experiences to mark the occasion of the 11th National Eosinophilic Week 2025, and asks Australian specialists to please consider learning more about this rare, but potentially devastating condition. An education program on EGPA is coming soon to the limbic – enter your details below to be notified when it is available.

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EGPA education on the limbic

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Thank you to AstraZeneca for providing an unrestricted educational grant that made it possible.

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