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

Last news

25 September, 2016

Alberto Soler achieves his challenge “Solidary Ironman for Cystic Fibrosis”

Our friend Alberto Soler Martínez has far exceeded its challenge of ‪#SolidaryIronmanforCysticFibrosis‬, reducing its forecast in two hours and has also raised the amount of € 1,623.00 for […]
20 September, 2016

Course of Autogenic Drainage level I

The Respiralia Foundation and the Cystic Fibrosis Balearic Association organized the course Autogenic Drainage Level I from 16 to 18 September 2016.
30 August, 2016

A very supportive anniversary

Who says that society is losing values? Our friend Luis De la Fuente and his friends show us that it is not true. Luis celebrated his […]
1 August, 2016

June-July 2016 Bulletin

You can check all the news regarding the people with Cystic Fibrosis of the Balearics in our monthly bulletin. Here you have the June-July 2016 bulletin.
8 July, 2016

Course of Autogenic Drainage Level II

The Respiralia Foundation and the Cystic Fibrosis Balearic Association organize the course of Autogenic Drainage Level I from 28 to 29 October 2016.
5 July, 2016

Success at the XVII Swimming Tour around Formentera against Cystic Fibrosis

240 swimmers enjoyed the crystal clear waters of Formentera in an atmosphere of solidarity and companionship from 1 to 3 July.
27 June, 2016

Bellver Leo Club helps children with Cystic Fibrosis

The Leo Club of Bellver International College gives € 1,000.00 to the fight against Cystic Fibrosis, thanks to a new solidarity campaign.
21 June, 2016

The spot of the Respiralia Foundation about its 10th anniversary awarded at Publifestival Social 2016

The spot “When I grow up” commemorating the 10th anniversary of the Respiralia Foundation, altruistically produced by Películas Suecas, has received the Award for best creativity […]
13 June, 2016

Carlos, a very supportive boy

Our friend Carlos celebrated his communion in a very supportive way. Thanks to his initiative, Carlos and his family donated € 100.00 to improve the quality of […]
3 June, 2016

Cystic Fibrosis vs. Medicine, by Alba

Alba Pérez-Aragón tells us in this article published at the Cystic Fibrosis Spanish Federation magazine what means for her to face the situation of being doctor and patient with […]

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