Our friend Alberto Soler Martínez has created a challenge:#IronmanporlaFibrosisQuística. He will swim 3,800 meters, cycle 180 km and run 42 km on September 24 in Mallorca, to raise € 2.500,00 for improving facilities of the Respiralia Foundation and the Balearic Association of Cystic Fibrosis. Read more
240 swimmers enjoyed the crystal clear waters of Formentera in an atmosphere of solidarity and companionship from 1 to 3 July.
The Leo Club of Bellver International College gives € 1,000.00 to the fight against Cystic Fibrosis, thanks to a new solidarity campaign.
The spot of the Respiralia Foundation about its 10th anniversary awarded at Publifestival Social 2016
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 life of children and young people with Cystic Fibrosis from Menorca. With more examples like Carlos our society would be much fairer. Our sincere thanks to him and his family.
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 Cystic Fibrosis at the same time. No doubt, it is a reflexion full of life.
The Rotary Club Calvia invited Carlos Pons, Managing Director of the Respiralia Foundation, to give a talk about Cystic Fibrosis at the weekly meeting of this prestigious Club. Kate Mentik, promoter of this invitation, will be the new President since July.
The Cystic Fibrosis Balearic Association has received a grant from the Menorca Island Council for the Integral Care Service for Persons with Cystic Fibrosis from Menorca. Read more
Películas Suecas, with Adam and Edu at the head, have created this fantastic spot to commemorate the 10th Anniversary of the Respiralia Foundation. With this video we want to convey optimism about the future of the treatment of Cystic Fibrosis. We have come a long way since we started working, but we need to make it to eradicate the disease.