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.
From July 1 to 3 you will be able to live a new edition of the Swimming tour around Formentera against Cystic Fibrosis. It will be its 17th edition. From now, you have activated the link to the inscription form, but remember that you can’t use until May 1, at 00:00 a.m. You dare? If you have Cystic Fibrosis, you have the inscription for free and you and your team have reservation priority from April 15 to 29. If that is your case, send us an email to email@example.com. More information here.
Today, Wednesday April 27, we commemorate the National Day of Cystic Fibrosis
The Cystic Fibrosis Association of the Balearics is a non-profit organization that works to improve the quality of life of children with Cystic Fibrosis and to raise awareness about this disease.
We recently received as a gift a 2015-16 Chelsea’s signed T-shirt with its authenticity certificate, and we would like to raffle it to raise money for the treatment of these children.
The T-shirt is framed to preserve it from damage, and it has the signatures of the 2015-16 team players.
The Balearic Hotel School and the Respiralia Foundation organized the annual high-calorie workshop for children with Cystic Fibrosis
Obra Social La Caixa donates € 5,000.00 for the improvement of quality of life of children and young people with Cystic Fibrosis. Read more