Welcome to the Respiralia Foundation and Cystic Fibrosis Association of the Balearics

Last news

13 November, 2017

Más muestras de solidaridad con el Desafío Respiralia

The members of the Royal Spanish Rock Climbing Society Peñalara continue to help publicize Cystic Fibrosis with the deployment of the Respiralia Challenge banner in their […]
7 November, 2017

October 2017 Bulletin

Check all the news about us in our monthly bulletin. Here you have the October 2017 bulletin (Spanish version).
6 November, 2017

2017 Rose of the Sea Fiesta against Cystic Fibrosis

For the eighth consecutive year, the Respiralia Foundation and the Cystic Fibrosis Association of the Balearics organized a new edition of the Rose of the Sea Fiesta […]
2 November, 2017

The IMAS helps the Cystic Fibrosis Association of the Balearics

The Consell de Mallorca, through the IMAS, has awarded a grant of € 5,400.00 to the Cystic Fibrosis Association of the Balearics for its project of […]
31 October, 2017

7th Solidarity walk against Cystic Fibrosis held in Ciudadela

210 people joined the 7th edition of the Solidarity walk held in Ciudadela on Saturday October 28, thanks to the initiative of Mollie-Ann and Becky Borràs.
31 October, 2017

2017 Christmas Lottery

One more year, the Cystic Fibrosis Association of the Balearics offers its lucky number in the draw for the Christmas Lottery on December 22, 2017: #79,133
23 October, 2017

Continued training with ProfessorJean Chevaillier

Continuing with our program “Educate equals Health in Cystic Fibrosis”, the Respiralia Foundation and the Cystic Fibrosis Association of the Balearics have organized a clinic on […]
11 October, 2017

Lecture about Autogenic Drainage and Cystic Fibrosis at Manacor Hospital

Invited by the Nursing Department of the Manacor Hospital, the Respiralia Foundation and the Balearic Association of Cystic Fibrosis gave a lecture on Autogenic Drainage and […]
10 October, 2017

Bankia helps the Respiralia Foundation

The campaign “En acción” of Bankia, within its Solidarity Network 2017, collaborates in projects to improve the quality of life of children and young people with […]
10 October, 2017

First meeting among adults and adolescents with Cystic Fibrosis

This meeting is due to the fact that the parents of the adolescents saw the need for their children to hear experiences of other people with […]

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