Cystic Fibrosis:
Unlimited Breath
Cystic fibrosis affects the breath of thousands of people worldwide. 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 strives for a better quality of life for patients and their families, for a life with Breathless Breath! Learn more about Cystic Fibrosis and support our work.
The areas of our actions
Advocating for CF patients & caregivers
Supporting CF community
Supporting CF centers
Access to medicines & treatments
Supporting lung transplants
Informing health professionals
Promotion of research
Collaboration with stakeholders
Prevention & early diagnosis
Public awareness
Prix Galien Greece 2021
We were awarded the Prix Galien Greece 2021 for the start of the early access program to revolutionary treatment for CF patients in Greece.
Second chance for life
We support organ donation
"Secret Mission C.F."
The first interactive children’s book on Cystic Fibrosis in Greece for children and adults
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
"Breathless Breath"
The first national helpline for Cystic Fibrosis in Greece
Our team is at your side to guide you and answer any questions you may have about the most common hereditary disease.
Call us at 2110-137700 every Tuesday: 11.00-15.00, 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
Patients and their families share their experiences, their concerns, their thoughts and the challenges they face in their life with CF, 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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November 26, 2024 41 Years Panhellenic Cystic Fibrosis Association – New Board of DirectorsWe are pleased to announce the formation of the newly elected Board of Directors of our Association, which...
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November 20, 2024 18-24 November 2024- European Cystic Fibrosis WeekA week dedicated to informing and raising awareness about the most common hereditary disease with more than 80,000...
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November 15, 2024 For Marianna and for every patient: The Cystic Fibrosis racing team ran the 41st MarathonThe runners of the racing team of the Panhellenic Cystic Fibrosis Association dedicated their medals to the patients...
We are members of European Organisations
Our supporters
The website has been redesigned with the kind support of Vertex Pharmaceuticals and Chiesi Hellas
