Rufina has a genetic disease of cystic fibrosis. Because of a breakdown in her genes, her body does not work properly: thick sputum stagnates in her lungs, and her digestive system lacks enzymes, so food is not absorbed. Children with this diagnosis can grow up and live a long and full life, but they need medicine for this. Unfortunately, Russian children are not getting enough medicine; they live less than they could and suffer from frequent and severe exacerbations.
One of the drugs that Rufina constantly needs is the antibiotic Fluimucil: when they have it, the girl comes to life, exacerbations are easier and occur less often. But it is necessary to interrupt the reception, as the fever rises and keeps day and day, the pain in the chest increases, the girl starts to choke. Unfortunately, such breaks in treatment are occurring more and more often: Rufina does not receive the necessary amount of drugs, and there is nothing to buy their family - for the course of treatment you need 193 200 rubles.
Rufina is now 15 years old. She - loves to read and draw, a calm and modest girl who, unfortunately, is very lonely. As long as the exacerbation is not removed and her lungs breathe half, she can not actively live, communicate and learn. And exacerbations occur more and more often, because there is no medicine. Help her to continue to heal and live!
