The “Respiralia Ambassador” Program of the Respiralia Group is an initiative to recognize those people or companies that support our cause. We are proud of all the people who support our cause and help us in the fight against Cystic Fibrosis. At the request of all the people who often ask us how they can […]
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Normalising Cystic Fibrosis in schools from the common sense
In this informative capsule, Miki Mayans explains how Cystic Fibrosis should be normalized in schools from the common sense, after his experience with students with CF. The beginning of the school year for a child with Cystic Fibrosis September is starting and, with it, a new school year. For many families with children with Cystic […]
Update on the HIT-CF Europe research project
The European CF Association (CF Europe) has published new information on the HIT-CF Europe research project for people with CF and rare mutations. People with CF with rare mutations This project aims to evaluate the efficacy and safety of different drugs (CFTR modulators and others) in people with CF and rare mutations based on intestinal […]
