Do not let Vika suffocate

Vika was born in the morning of November 9, 1996. Her mother was still lying on the delivery table when a pediatrician, after examining the child, offered her to abandon the child: "Woman! Your child has shortened upper limbs. She was born with multiple signs of chromosomal abnormalities. Feel free to relinquish your parental rights. Believe me, you will not be condemned”. It only took her five seconds to make the right decision: "I will never give up my girl!"

That first day in the hospital, mother spend sobbing. She held Vika in her arms and asked for forgiveness because she brought her into this world as a sick person. Head full of the same questions: "Why me? Why did I give birth to a sick child? For what God is punishing me? What will people say? "

On the second day, Vicky got intestinal bleeding. Doctors have stated before the fact: "Mommy! Your girl cannot live until morning. We cannot stop the bleeding. Be brave and be ready for anything... "It was the first sleepless night, when her mother cried and prayed. It was the night she accepted her daughter as she was. She would love her and never leave.

In less than 19 years, doctors have not once prepared mother for Vika’s fatal outcome. And when it seemed that when there was no way out – the girl would survive!

Vika has many hard diagnoses. She suffers from a genetic disorder causing her short stature (her height is 1 meter 37 centimeters), delayed sexual development, the absence of the uterus, cannot produce the female hormone that entails destruction of the bone tissue.

At 2 years and 4 months, Vika got measles vaccination and after that, she began having nosebleeds. Even then, she survived, but earned a new disease for a lifetime. It periodically enters into remission but when relapse occurs, Vika gets into intensive care unit with an intestinal or nasal bleeding.

In addition, Vika suffers from kidney problems and diabetes. With all these diseases, mom learned to fight, but recently, a tumor was found in girl’s left lung. Surgery and a new diagnosis: lymphocytic pneumonia, a rare disease in which the lungs are covered with small granules that could degenerate into a tumor. Vika is often cannot get enough air, suffers from asthma attacks and each day may be the last.

In addition, Vika has severe degree of myocardium. At any time, a heart attack can occur. Cardiologists unable to help. It is the result of lung disease, which in Ukraine, unfortunately, cannot be cured. Last hope - examination in Israel. We must have time to help! There is no other way! Children should not die because of the lack of money!

This project was canceled, the amount collected is 2 670 UAH. The funds were disposed of in accordance with the Rules, Principles, and Procedures of the Ukrainian Philanthropic Marketplace (UBB) International Charitable Fund and the decisions of the Project Donors.

Name: Victoria Y. prysiazhna, born 09.11.1996

Location: Poltava region, Kremenchuk

Diagnosis: lymphocytic pneumonia, Turner's syndrome, diabetes mellitus type II, thrombocytopenic purpura, chronic pyelonephritis