Welcome to EGPA.info, a site dedicated to those diagnosed with this rare and challenging autoimmune condition. EGPA occurs in 2-3 new cases per year per million people, which means you are selected with almost impossible odds to belong to this unique group! OK, not what you had in mind but we hope that somewhere in these pages you can find a way to make sense of it all.

Plato says that the unexamined life is not worth living. But what if the examined life turns out to be a clunker as well? Kurt Vonnegut

Walk through the process.

What is on this site?

EGPA can arrive and present itself in many ways but there is generally a point at which the diagnosis is confirmed, which we address in the 'Crash' section. The 'Recover' and 'Live' sections are there to help with how to get your life back into some kind of new normality. You are in charge!


We ask questions like 'Is this really happening?', 'Why ME?' and talk through what might happen next.


Recovery is obviously hugely important and there must be close collaboration between you, your medical team and those around you. We talk through the issues and compare it to climbing a mountain. Mountain air is good, right?


There are many challenges and we could easily be dragged down into the negatives but there is absolutely no reason why life after EGPA should be worse than before. So we look through the issues and hope that you will give feedback on what has kept you motivated to defeat this barefaced attempt to steal your life!


There is still much to do in this section, so please keep coming back. You will find a mixture of easy reading and highly technical including a glossary of medical terms that often come up in the context of EGPA.

Friends and family.

If you are a friend or family of a newly diagnosed sufferer then stop off here.

Friends and family

Recently Diagnosed?

Finding out more.

We hope these pages will help as you work your way through the many issues and questions. Moving along the menu above, from left to right, will help order things for you, particularly if you have been recently diagnosed.

Feeling alone?

You are not going to be left alone with these medical tongue twisters. There are new drugs, better treatments and many who have been there before you and are ready to help.

Keep learning.

Once you have got to grips with your condition and you feel ready to learn more, have a look at our resources section to find out what is happening in research, or just to read some of the interesting commentary, blogs, FAQs etc. Tip, dont get into medical papers too quickly, the language is difficult and older papers can reflect an outdated prognosis.

What is the acronym?

EGPA stands for "Eosinophilic Granulomatosis with Polyangiitis!"

Churg-Strauss Syndrome (CSS) is the old name, still used by many, but this is slowly changing, particularly in medical documentation.


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contact us at admin@egpa.info

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Latest News

Camille Pagán writes a personal message to EGPA sufferers.

Camille Pagán, Author, with a passion for health and nutrition has sent a personal message to EGPA sufferers.
"I don't know how it feels to have EGPA, but as a health writer and editor who has spoken with hundreds of people coping with difficult diagnoses, I've been told that laughter and hope make the day-to-day more bearable. I hope that my book will bring you a little levity and light."
She was thrilled that her book 'Life and Other Near-Death Experiences' has been listed in our Good Reads and wishes us all the best.

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