The DinoSol Foundation, along with Canary Islands musician Iván Torres from the group “Efecto Pasillo” and Benito Mayor, president of the Oliver Mayor Foundation, has launched the initiative “A Small Gesture, A Big Step Against Cystic Fibrosis” on Thursday, 22 October. This programme, which first took place in 2025, aims to raise funds to create an exercise room for the treatment of individuals with cystic fibrosis through contributions collected.
From today, HiperDino is selling 10,000 solidarity bags in its stores for just £2 each, with all proceeds going towards the new exercise facility for cystic fibrosis patients.
Davinia Domínguez, President of the DinoSol Foundation, emphasised her organisation’s commitment to improving the lives of those facing health challenges. She stated, “Our initiative this year reflects our dedication to providing necessary resources that can help enhance the quality of life for patients affected by this condition.”
Iván Torres highlighted the importance of such initiatives in fostering a more cohesive and supportive society. He noted, “This effort will mark a significant change for cystic fibrosis patients, as the creation of a rehabilitation space will greatly improve their wellbeing.”
Cystic fibrosis, also known as mucoviscidosis, is a common genetic condition that causes the body to produce thick, sticky mucus, obstructing the lungs, pancreas, and other organs. In Europe, it affects around 1 in 2,500 newborns, making its incidence approximately 4 in every 10,000 births, and it is the most prevalent hereditary condition among Caucasians.
In the Canary Islands, about 200 individuals are diagnosed with cystic fibrosis. In 2004, there were 51 hospital admissions for this condition, with 29 male and 22 female patients, and an average age of 19. The average age for patients in the eastern islands is 25, compared to 12 in the western islands. Over the past four years, the average age of hospital admissions in Las Palmas has risen from 19 to 25, while in Tenerife, it decreased from 13 to 12.
The Oliver Mayor Foundation for Cystic Fibrosis offers support and guidance to those affected by the disease and their families. Established as an association in November 1991 and later becoming a foundation in 2004, it was founded by parents concerned about the lack of resources for treatment. This foundation is named after the founder’s son and brother, who passed away from cystic fibrosis.
Among its projects, the Oliver Mayor Foundation focuses on the protection and care of individuals disabled by cystic fibrosis, extending support to their families and caregivers. It promotes training in care skills and collaborates with both public and private institutions through various initiatives.
