European CF Awareness Week, 20-25 November 2023
40 years Hellenic Cystic Fibrosis Association
Unlimited Breath
Visit the reconstructed website of Hellenic Cystic Fibrosis Association www.cysticfibrosis.gr to learn more about the most common genetic in caucasian population. The reconstructed website is bilingual, fully compatible with android, iphone, tablets, etc., with new updated content.
- what is CF, prevention & early diagnosis
- treatments and specialized CF Centers in Greece
- guide of benefits for CF (health, socio-economic, allowances, education, work, retirement, etc.)
- HCFA’s actions (conferences, awareness campaigns, support of patients & CF Centers, HCFA’s awards, etc.)
The reconstructed website will host stories from CF patients, caregivers, members of family and friends, who will share their experience of living with Cystic Fibrosis, their thoughts and the challenges they face, the good days and the difficulties. Are you a CF patient or a caregiver, member of family or friend? Send us your story now to cysticfibrosis.gr@gmail.com
* You can send us a text of your story you wish to share (with your photo optionally) or a video with your story. You can send us your name or remain anonymous.
