In this new informative capsule, Esther tells us about the initiatives that she and her family have had to help the Cystic Fibrosis Balearic Association to achieve its objectives. An up-and-down start Esther is the mother of Leia, a 5-year-old girl. After a false negative, Leia was not diagnosed with Cystic Fibrosis until she was […]
normalización de la FQ
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 […]
