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 firstname.lastname@example.org. 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
Clinica Aliviam and Respiralia Foundation signed an agreement for the project “Active Living Without Pain”.
Oris donates € 8,833.00 to the Respiralia Foundation thanks to the draw of the watch that Carlos Coste used to get his Guinness record of horizontal apnea in the Cenote Dos Ojos of the Rivera Maya.