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.
Our 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 C.F."
The first interactive children’s book about Cystic Fibrosis in Greece for children and adults. Distributed free of charge
Let’s discover how we can face every difficulty in life and turn all the “NO’s” that make it difficult for us into those “YES’s” that bring us joy!
Helpline
"Unlimited Breath"
Panhellenic Support Line
Our team is at your side to answer any question you may have about the most common inherited disease.
Call us at 2110-137700 Every Wednesday & 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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December 8, 2025 Podcast about Cystic Fibrosis and the “Secret Mission: CF.”A special podcast dedicated to Cystic Fibrosis and the "Secret Mission: CF", featuring the children's book author-illustrator, president...
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December 8, 2025 Interview with ERT. Despina Gini, Deputy Treasurer of the Association, talks about life with Cystic FibrosisA human and moving interview with Despina Gini, Rev. Treasurer of the Panhellenic Cystic Fibrosis Association, and member...
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December 5, 2025 Establishment and 1st meeting of the Lung Transplant Working GroupAs it has been announced, the Panhellenic Cystic Fibrosis Association, in the context of continuous patient support and...
Membership in International Bodies
Supporters
The website was rebuilt in 2022 with the kind support of Vertex Pharmaceuticals and Chiesi Hellas
