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 distinctive educational campaign for 3rd, 4th, 5th, and 6th grade primary school students. Because the code CF² stands for Cystic Fibrosis and Classified Faculties, the hidden abilities and strengths every child carries within when facing any challenge in life.
Starting from 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 and Discover your Classified Faculties!
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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July 17, 2026 Wish you a great summer with Unlimited BreathHave a great summer from the Panhellenic Cystic Fibrosis Association! 🏖️🌞 It's time to rest, relax, and enjoy...
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July 15, 2026 EURORDIS Mental Health Survey- Cystic Fibrosis Psychological Support GroupsA new European study by EURORDIS—Rare Diseases Europe highlights the significant mental health burden on people with rare...
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July 13, 2026 The Panhellenic Cystic Fibrosis Association at the 49th European Cystic Fibrosis Congress (ECFS 2026)The Panhellenic Cystic Fibrosis Association participated in the 49th European Cystic Fibrosis Congress (ECFS 2026) in Lisbon, sharing...
Membership in International Bodies
Supporters
The website was rebuilt in 2022 with the kind support of Vertex Pharmaceuticals and Chiesi Hellas
