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
Second chance for life
We support organ donation
"Secret Mission C.F."
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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December 20, 2024 Gold Award for the campaign “Breathe Unlimited Breath – Be a Life Donor”: for Marianna and every patientThe Gold Healthcare Business Award 2024 was won by the Panhellenic Cystic Fibrosis Association for the innovative campaign...
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December 17, 2024 Panhellenic Cystic Fibrosis Conference 2024 “Discovering the Path to Unlimited Breath”Conclusions from the Panhellenic Congress of Cystic Fibrosis 2024 The Panhellenic Cystic Fibrosis Conference "Discovering the Path to...
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December 12, 2024 4th cycle of psychological support groups startsFollowing the excellent results of previous years, the free psychological support groups for Cystic Fibrosis patients and caregivers...