The Association HCFA-TEAM February 15, 2023

The most common genetic disease in the caucasian population

40 years Hellenic Cystic Fibrosis Association (HCFA)

We raise awareness for the disease and the prevention

We fight for “Breath Unlimited” for patients with Cystic Fibrosis all over Greece

Our actions areas
Defending patients' rights
Empowering patients and caregivers
Supporting CF Centers
Access to medicines and innovative treatments
Lung transplants support
Informing health professionals
Research programs support
Collaboration with authorities & stakeholders
Disease prevention & early diagnosis
Raising public awareness

We were awarded with Prix Galien Greece 2021 for advocating for the start of early access program to the revolutionary treatment for patients with Cystic Fibrosis in Greece.

A second chance at life
We support organ donation
We provide to our patients
Children's book
Secret mission: CF

The first interactive children’s book for Cystic Fibrosis in Greece

For young and old CF patients, their caregivers, and for anyone who wish to discover the mystery of the disease and unlock its secrets.

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Carriers of the disease in Greece
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possibility for 2 carriers to have a baby with CF
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CF patients in Greece
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Gene mutations of the disease
CF patients in Europe
Living with Cystic Fibrosis

CF patients and their families share their experiences, concerns, thoughts, and challenges living with Cystic Fibrosis, the good days and the difficult times.

Are you a Cystic Fibrosis patient, parent, caregiver, relative or friend who wants to share your story?

Our News
Member of International Organizations
Our Supporters

The website was reconstructed with the kind support of Vertex Pharmaceuticals and Chiesi Hellas