Who we are HCFA TEAM February 15, 2023

The Hellenic Cystic Fibrosis Association (HCFA) is a non-profit association of patients. It was founded in 1983 in Athens and represents Cystic Fibrosis patients and their families nationwide.

The Association plays a leading role in the support of patients with Cystic Fibrosis in every corner of the country, aiming at the unified and dynamic representation of all patients with Cystic Fibrosis at a national level. The Board of Directors is composed of patients and parent-caregivers from the Cystic Fibrosis Centers at the Children’s Hospitals-Agia Sophia, Sismanoglio, Hippocrates Hospital of Thessaloniki, Papanikolaou Hospital, as well as the Lung Transplant Monitoring Center at Attica Hospital.

It is one of the oldest patient associations in Greece. During its 41 years of operation, it has managed to change the “map” of the disease in Greece. Through the collective effort of all its members, it improves the quality of life of patients and ensures their active participation in decisions and actions concerning their health and rights.

The Association is registered in the Greek National Registry of Non- Profit Private Sector Social Care Agency and in the Greek Registry of Voluntary Non- Governmental Organizations (NGOs).

The Association is a founding member of the Greek Patients Association and the Rare Diseases Greece (RDG) and it’s a member and representative of Greek CF community in European organizations.

Members of the Board of Directors

Anna Spinou
President
Constantina Giannaki
Vice President
George Plala
Secretary General
Nadia Proga
Treasurer
Christos Bakodimos
Rev. Secretary
Despina Gini
Rev. Treasurer
Marilena Tsentidou
Member of the Board

Alternate Board Members

Melina Tiglianidou
Rev. Board Member
Stella Georgaki
Rev. Board Member
Maria Paliou
Rev. Member of the Board.

Our Partners

Stavroula Rakitzi
Volunteer Psychotherapy Group Coordinator
Eleni Saltouridou
Cystic Fibrosis Helpline Manager
Rena Pavlidi
Cystic Fibrosis Hotline volunteer
Dionysis Chionis
Legal Advisor

Scientific Committee

The Panhellenic Cystic Fibrosis Association is supported by a Scientific Committee, which consists of scientists specialized in Cystic Fibrosis from all hospitals in Greece, where patients are monitored and treated.

The mission of the Scientific Committee is to support and advise the Board of Directors on medical and other related issues, aiming at the scientific establishment and medical documentation of the positions and actions of the Association.