Empower someone today. 💙 Share APFED's free webinar library — real education from trusted experts, designed for the eosinophilic disease community. Visit apfed.org/webinars.

Living with eosinophilic disease takes resilience that most people will never fully understand. We want to know: what keeps you strong? Share your source of strength in the comments and let's

Do you have a favorite photo from an APFED event? A conference moment, a Walk for HOPE memory, a connection that changed everything? 🫶 We want it in our time capsule. APFED is collecting photos, m

1 in 700 people have EoE. Most wait 4 to 6 years for a diagnosis. That has to change, and it starts with advocates like you. Download APFED's EoE Advocacy Toolkit and take action today.

APFED has spent 25 years building resources for patients and the clinicians who care for them. Help us get those resources into the right hands and share apfed.org with your provider today.

Researchers are developing better tools to predict EGPA flares, a new oral treatment for eosinophilic asthma just received FDA Fast Track designation, and early trial results for an EoE injection t

Share. Learn. Give. Advocate. Every action matters, and together, they've built 25 years of impact for the EOS community. What will your next step be? Join the movement at

How long did it take to get your diagnosis? For many in the eosinophilic disease community, the answer is years and years of symptoms, specialists, and searching for answers. Your journey is not ju