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 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

Become an organ donor

Children's book

"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!

Get the book for free

Helpline
"Unlimited 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: 14.00-18.00 (EET), Wednesday & Thursday: 16.00-19.00 (EET) or email us at helpline@cysticfibrosis.gr or chat with us live in the website chatbox and on social media.

We provide patients with

Atomic spirometers,
nebulizers
& portable
condenser

psychotherapy groups for

CF patients and

caregivers

Online

support meetings

meetings

(coffee breaks)

Carriers of the disease in Greece

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Mutations in the Cystic Fibrosis gene

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Patients with Cystic Fibrosis in Greece

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Children are born with Cystic Fibrosis every year in Greece

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Patients in Europe

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?

Send us your story

Our news

Our News
February 21, 2025 February 22, 2025New Year’s Cake Cutting & Coffee Break
Dear members, We invite you to the online cutting of the New Year's cake of our Association, which...
Our News
February 15, 2025 February 22, 2025Unlimited Breath: free exercise programme for patients with Cystic Fibrosis starts
We are very pleased to announce that the Panhellenic Cystic Fibrosis Association in collaboration with the DanceNikol dance...
Our News
January 4, 2025 January 24, 2025In Memory of Marianna – We become Organ Donors
The new year finds us with sad news, as we are deeply saddened to announce the loss of...