Cystic Fibrosis
Unlimited Breath
Cystic fibrosis affects the breath of thousands of people worldwide from the moment they are born. It is the most common inherited disease,a serious genetic disease that mainly affects the lungs and pancreas, making breathing and digestion difficult.
The Association fights for Unlimited Breath for every person with Cystic Fibrosis! Learn more about Cystic Fibrosis and support our work.
The areas of our actions
Prix Galien Greece 2021
We saved lives and gave Unlimited Breath! Thanks to our efforts, in collaboration with the Ministry of Health and the competent authorities, Greek patients with Cystic Fibrosis gained early access to the revolutionary treatment that “freezes” the disease before it was approved in Europe. A victory for life, awarded with the Prix Galien Greece 2021, the “Nobel Prize of Pharmacy”!
Second chance for life
We support organ donation
"Secret Mission: CF²"
A special educational campaign for students of 3rd, 4th, 5th and 6th grade of elementary school. Because the code CF² means Cystic Fibrosis and Classified Faculties that every child hides inside when faced with any difficulty in life.
On the occasion of an invisible difficulty, Cystic Fibrosis and lung transplantation, we cultivate in all children empathy, acceptance, imagination and inner strength for every “mission” that life brings.
Learn, Feel, Inspire!
Helpline
"Unlimited Breath"
Panhellenic Support Line
Our team is here to answer any questions you may have about Cystic Fibrosis and lung transplantation.
Call us at 2110-137700 Every Tuesday & Thursday: 4pm-7pm or email us at helpline@cysticfibrosis.gr or chat with us live in the website chatbox and on social media.
Living with Cystic Fibrosis
We share our experiences, our concerns, our thoughts and the challenges we face in our daily lives, the good days and the difficult moments.
Are you a Cystic Fibrosis patient, caregiver, relative or friend? You wish to share your story?
Our news
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March 11, 2026 7th Cystic Fibrosis Workshop of the Department of Cystic Fibrosis – Agia SophiaThe 7th Cystic Fibrosis Conference of the Aghia Sophia Children's Hospital will take place on 14 March 2026...
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February 28, 2026 28 February 2026 – World Rare Disease Day28 February is dedicated to World Rare Disease Day. More than 300 million people worldwide live with a...
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February 26, 2026 Good journey to Despina Gkinis, Deputy Treasurer of the Panhellenic Cystic Fibrosis AssociationIt is with deep sadness that we bid farewell to Despina Gini, Deputy Treasurer of the Board of...
Membership in International Bodies
Supporters
The website was rebuilt in 2022 with the kind support of Vertex Pharmaceuticals and Chiesi Hellas
