The association Mukoviszidose eV finances its work for the benefit of those affected mainly from donations. Due to the rarity of the disease, it is difficult to find hearing in public. For this reason, the public campaign "What do I want?" Started on November 8th and will last until shortly before Christmas. Six stories are about people in and about Mukoviszidose eV with their diverse careers, wishes and goals.

You can find more information at  https://blog.muko.info/