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Maria Dietrich 22.09.2017
MOOCI helps people affected by mucoviscidosis with reconstructive surgery
Restoring a piece of normality – this is what the MOOCI CEO Janis Jung would like for those affected by CF. His network makes it possible to have certified aesthetic and reconstructive surgeons perform corrections on mucoviscidosis patients, for example by treating scars after a lung transplant. -
Maria Dietrich 14.02.2017
Media groundbreaking for ATMOS
Daring the greatest feat possible: stamping out the hereditary disease mucoviscidosis and establishing a place of creativity in a large-scale European effort. And already a close alliance is forming: Supporters in the cultural, construction and creative industries as well as medical and health care services are standing together for the media groundbreaking of ATMOS at the Coop Himmelb(l)au studio. -
Chris Müller 13.02.2017
My child has an incurable disease – but I will never give up
The diagnosis came out of the blue. Shortly after our child was born six years ago, doctors found that our baby had mucoviscidosis – a metabolic disease that is still incurable. -
Maria Dietrich 02.02.2017
Benefit kick on may 19, 2017
Eleven years ago, Michael Kosch and Walter Fleischhacker organized the first Benefit Kick for children with mucoviscidosis. As a result, Kick for Kids already raised donations of about € 150,000. The next kick-off for a benefit game is at ASKÖ Donau Linz/Linz AG Arena on May 19, 2017.
