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

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 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

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"

Panhellenic Line

Our team is at your side to answer any question you may have about the most common hereditary disease.
Call us at 2110-137700 every Tuesday: 14.00-18.00, Wednesday & Thursday: 16.00-19.00 or email us at helpline@cysticfibrosis.gr or chat with us live in the website chatbox and on social media.

Next to every person with Cystic Fibrosis

🤝 Support & Counselling

Helpline

Psychotherapy groups

Community support

💪 Health & Wellbeing
Pilates Exercise Programme
Respiratory Rehabilitation
Respiratory Equipment Provision

📚 Knowledge & Rights
Information tools
Guide to benefits
Online community

carriers of the disease in Greece

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mutations in the cystic fibrosis gene

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Cystic Fibrosis patients 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

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?

Send us your story

Our news

Our News
April 15, 2025 April 15, 2025Happy Easter with Unlimited Breath for all!
The Panhellenic Cystic Fibrosis Association wishes you a Happy Resurrection and a Happy Easter with Unlimited Breath for...
Our News
April 15, 2025 April 15, 2025Interview with our President in Health Today magazine, March 2025 issue
Under the title "With a vision of Unlimited Breath for 2025", Health Today magazine hosts in its March...
Our News
April 10, 2025 April 14, 2025Our President Anna Spinou joins ERN-LUNG – Stable European participation in the EURORDIS Board
A strong European voice for Cystic Fibrosis We are very pleased to announce that as of January 2025,...