Disponible en / Available in: Español
The Respiralia Foundation and the Cystic Fibrosis Balearic Association present its 2021 Magazine about Cystic Fibrosis, a report of activities carried out in 2020.
Design change
Although the physical format is the same, Juan Roig, from the company Verbigrafía and ambassador of the Respiralia Foundation, has made a design change to make it more attractive.
The content
2020 has been a very special year. We needed to tell how we have adapted to a new situation that, far from intimidating us, has motivated us to improve and to take advantage of tools that we did not use before.
The collaboration of people with Cystic Fibrosis, doctors, epidemiologists and participants of our events has inspired a very participative magazine, in which all our stakeholders have their share of protagonism.
What can we find?
Covid-19, as it could not be otherwise, has its protagonism in a good part of the magazine, but always from a positive point of view. The interview to Dr. Borja Osona, pediatrician specialist in Cystic Fibrosis, or to Dr. Jordi Reina, head of the Virology Unit of the Hospital Son Espases, answer many of the questions asked by the group of people with CF.
But, in the Respiralia Foundation and the Cystic Fibrosis Balearic Association we have the people who have this disease in the center of our activities, so his opinion about the situation we live in 2020 was basic.
Laura, Alba, Jorge, Carlota, Maria and many others tell us about their experiences, both with the pandemic and with new medications they are fortunate enough to be taking.
Great ambassadors of the Respiralia Foundation
Last year we had to go to Formentera virtually through the Corona-Tour. We gave a Tour of Formentera marked by a positive view of the pandemic. The participation of the Respiralia “family” was key to save a complicated year economically, but also to change the negative and depressive trend that had been installed in society.
This participation, translated into photos and videos with positive messages and support to the group of people with Cystic Fibrosis and in the interviews of the presentation of the institucional video produced by Películas Suecas, is transferred to the magazine with spectacular opinion articles, such as the one by Juanjo.