On the occasion of World Disability Day on 3 December, we talk openly about the “invisible” disability of Cystic Fibrosis. A chronic and progressive disease that affects the daily lives of thousands of people and families.

In an interview with Queen.gr, the President of the Panhellenic Cystic Fibrosis Association, Anna Spinou, shares her experience as a patient and the daily challenges faced by those living with Cystic Fibrosis, while shedding light on the strength, perseverance and the need for equal access to health and society.

Cystic fibrosis is an invisible disability with very visible needs.
We need continuous support, education, access to new treatments, social understanding and a health system that responds to the real needs of patients.

🔗 Read the interview here:
https://www.queen.gr/well-being/ygeia/story/313807/i-kystiki-inosi-einai-mia-aorati-anapiria-me-poly-orata-provlimata

Together we continue the struggle for a life with Breathless Breath, dignity and equal opportunities for all.