Khadija has a genetic disease, she needs to come to the hospital to adjust her treatment.

Since birth, Khadija has been diagnosed with congenital heart disease and a rare genetic skin disease – epidermolysis bullosa. The girl's toenails became deformed, her gums began to bleed, and her esophagus narrowed, causing problems with swallowing food - all these are typical complications of epidermolysis bullosa. Despite the difficulties, Khadija tries to lead a full-fledged lifestyle: she goes to school and loves to draw very much. Khadija is the only child in the family, she is raised only by her mother. The Butterfly Children Charity Foundation helps the girl with the purchase of necessary dressings and skin creams, as well as with the organization of hospitalization and rehabilitation. In order to stabilize the girl's condition and prevent further complications, she needs to be hospitalized. Now Khadija and another ward with the same diagnosis are waiting for doctors in Moscow. The guys need help in purchasing tickets to the capital and on the way back home. Let's help the children and their escorts get to the place of hospitalization!