The Cystic Fibrosis Spanish Foundation has asked the Congress of Deputies to join the commemoration of World Cystic Fibrosis Day, on September 8, approving an institutional declaration in which the Congress publicly expresses its solidarity with all the people who live with this disease and declare the Chamber’s commitment to the care and protection needs […]
Cystic Fibrosis news
The reconstruction plan of PSOE-Podemos leads to the extinction of patient associations
The Government endangers physical therapy sessions for children with Cystic Fibrosis, with the possible prohibition of aid from pharmaceutical companies to patient associations. Patient associations in Spain may run out of one of their main sources of funding and be doomed to disappearance. This is what the collective fears if the opinion of the Congress […]
The welfare, guidance and monitoring program increases its demand
In recent weeks, demand for the welfare, guidance and monitoring program of the Respiralia Foundation and the Balearic Association of Cystic Fibrosis has increased. Through this program we have carried out various actions before COVID, such as solving doubts about the adaptation of jobs for the coronavirus, issues related to adoption in families with Cystic […]