Advocacy Partner:
American Partnership For Eosinophilic Disorders (APFED)

The American Partnership for Eosinophilic Disorders (APFED) is a 501c3 nonprofit organization founded in December 2001 by a group of mothers of young children living with eosinophil-associated diseases. We are a patient advocacy group dedicated to improving the lives of those living with eosinophilic disorders.

Contact: Mary Jo Strobel – Executive Director
Phone: (713) 493-7749 Ext. 2
Email: [email protected]

Visit Site ♥ Donate

EoS Support Webinar Series

APFED’s EoS Support Webinar Series offers a virtual forum for patients and families to connect and learn. Join various experts for hour-long webinars on a variety of topics, such as diagnostics, treatments, and daily living with eosinophil-associated diseases, including eosinophilic granulomatosis with polyangiitis (EGPA).

Publishing Schedule: Monthly

Registration Link

EGPA Clinical Trial Data Recording: The 2025 Annual Patient Conference

APFED’s annual patient conference offers an engaging opportunity to connect with experts, hear the latest research updates, and learn practical strategies for living with eosinophil-associated diseases, including EGPA. This year’s program included findings from a recent clinical trial on eosinophilic granulomatosis with polyangiitis (EGPA)—visit apfed.org/conference to register at no cost to access the recordings.

Registration Link

APFED Connect Virtual Support Groups

APFED offers virtual support groups designed to help patients and caregivers connect, share experiences, and find community. This includes groups specifically for individuals living with rare subsets such as EGPA, HES, and EF.

Explore all available support groups and find the one that best fits your needs: https://apfed.org/support.

View All Events

About Advocacy Partners

The information above is provided by our partner. Learn more about our advocacy partners here.