Do not allow to kill the lungs. 2

Illya is 5 years old. He is a very active and busy child: he likes to play, have walks, and go for a cycle ride. But all these activities have to be postponed because the disease will not wait. First of all, all necessary procedures should be done, and only then he can have a short walk and needs to go back to the apartment because it's time to do inhalation and take medicines. Illya suffers from cystic fibrosis - a severe genetic disease that affects his entire body.

The lungs are being affected by the disease most of all.  They are filled with thick sputum, in which infections settle, so the boy should do inhalations, exercises and take medications several times a day. You can't miss it! The disease doesn't care if the child wants to ride a bike, run in the park, or go to the river with his parents. The family often visits their grandmother in the village, and sometimes there are disruptions of power there, and it becomes impossible to turn on a standard inhaler.

Illya needs to move a lot and be in the open air to cough up sputum better, but he is confined to the apartment due to his illness. The boy cannot relax and enjoy life. The dream of Illya's family is a small portable inhaler. The inhaler that will make it possible to do inhalations in the street and go cycling with the dad immediately and go to the village to gain strength. That it was possible to learn about this world, as all children do.

We kindly ask you to participate in the fundraising for a portable inhaler, sets of consumables for the inhaler, and product certificates that will help Illya eat better and have the strength to prevent cystic fibrosis from killing his lungs.