Eroski Baleares launches a new #Midesonrisas campaign to collaborate with 14 non-profit entities that work with children. You join?
The Cystic Fibrosis Association of the Balearics has created the challenge “Pass the salt” for children with Cystic Fibrosis to to give visibility to Cystic Fibrosis, to demand an agreement between the Ministry of Health and Vertex Pharmaceuticals so that doctors can have at their disposal the medicine Orkambi and raise funds on the platform […]
The Respiralia Foundation and the Cystic Fibrosis Association of the Balearics carry out the program “Educate equals Health in Cystic Fibrosis”. One of the pillars is to make known the Cystic Fibrosis to the youngest through the tale “Respiralio and the Big Blue Bear”.
Thanks to a project of the Cystic Fibrosis Spanish Federation, the Cystic Fibrosis Association of the Balearics will opt in 2019 to a seal of “Recognition of management and Social Commitment” created by the Develop Group and certified by Bureau Veritas. Several professionals and other interest groups are working hard to improve our entity. On […]
The Welfare Institute of Mallorca (IMAS) of the Consell de Mallorca approves a € 10,000.00 subsidy to the comprehensive care for children and young people with Cystic Fibrosis of Mallorca carried out in 2017. This project includes the program of welcome, orientation and follow-up; the training program in the technique of autogenic drainage, inhaled therapy […]
The Balearic Association of Cystic Fibrosis and the Health Service of the Balearic Islands (Ib-Salut) have signed an agreement of € 34,560.00 for the years 2018 and 2019, by which the Association is responsible for providing training in the technique of autogenous drainage, inhaled therapy protocols and hygiene measures for children and young people with […]