About Us
APACS APS, the Churg-Strauss Syndrome (or EGPA) Patient Association, is a non-profit organization created by patients, for patients. Our mission is to raise awareness, provide representation, and advocate for people living with EGPA and their families.
Our goal
Our goal is to support those in need by providing clear information about the disease, guidance on how to obtain exemptions, and details about referral centers. At the same time, we aim to engage general practitioners and specialists to build a fast and efficient network across Italy and Europe.
What is EGPA?
Eosinophilic Granulomatosis with Polyangiitis (EGPA), formerly known as Churg-Strauss Syndrome, is a systemic vasculitis that affects small- to medium- sized blood vessels.
Are you a clinician or a researcher?
We are always looking for specialists to join our network of contacts. There are many patients searching for referral centers in their area. Help us meet this growing demand.
We are also trying to engage General Practitioners (GPs) to enable faster diagnoses.
Are you a patient?
APACS APS helps patients and their families by offering practical and emotional support. Visit our website at www.apacs-egpa.org for
useful information, subscribe to our newsletter, become a member and follow us on Facebook, LinkedIn, and Instagram.
Become a Member
Everybody can become a member of APACS APS.
Becoming a member is fast and easy: just follow the instructions on https://apacs-egpa.org/iscrizione- rinnovo/ or scan the following QR code.
