I believe: you will help!

Unfortunately, you’ll never appreciate life so much, without recognizing a threat of it. Olya, who has cystic fibrosis, and her family ask us for help. To breathe normally, Olya needs to constantly take expensive medicine. 6 months of treatment will cost the sum that parents will never collect by themselves. Olya’s family is unable to pay for the course. Let’s help them!

The laugh of the child is a joy in the family. First steps, first successes. Life is beautiful. But each of us has our own way of life. Fate - at everyone, it makes life tests with which a person has to cope. So the trial, called Cystic Fibrosis, has appeared in Kazakov’s family and it happened when small Olechka was only1 year and 9 months. In 2007, the scheduled examination X-rays showed upper storey sided pneumonia, consequence - sticking the lung tissue, and complete failure of this region of the lung. Improve the child's condition seemed to be able to lung lavage due under general anesthesia, and these procedures were conducted 5 times. In autumn of 2013 after the procedure the situation remained unchanged and unresolved, and Olga was discharged home with atelectasis. Cystic fibrosis was progressing.

Severe illness has put its scope in life: learning at home, but the child's desire to be like her peers, provides an incentive to keep up with them in anything. Olga takes part, as far as possible, in the life of the class. Winter contest of drawing, on a free theme, found its winner, it was Olya, she drew a girl on horseback.

Child’s dreams are to become healthier and breeding horses, the most gracious animals in the world. And so far she has horses in the pictures on the inhaler, on clothes ... Natural, responsive and so adult in thoughts and actions girl - needs daily, expensive and so needed treatment. In raising funds to pay for medicine (Pulmozyme for 6 months) and Kazakov’s family refers to all caring people.

Name: Olga Kazakova, 11-year-old

City: Dnipropetrovsk

Diagnosis: Cystic Fibrosis