One in a million

Children with this diagnosis do not live - the mother was told in the hospital. And my daughter will live! - the mother of little Diana claimed to the entire world. Here you have the opportunity to help fulfill the promise of a courageous woman, and prove that love, compassion, faith make wonders! The only chance for the baby to survive is the bone marrow transplantation abroad, the money to pay for which the family would nether gather themself!

Dianochka was as an expected and so beloved even before birth kid! All of the family, the father and mother, and little sister Bogdanochka really wanted another baby in the family. Diana was the gift for the daddy 's birthday. With the birth of Diana the Chobans lived a simple life, enjoying every day. And after six weeks the baby got health problems that first looked trivial but ended with sepsis. And only when it happened again with high fever, doctors were able to establish a diagnosis - congenital neytropiniya. It is a rare disease. Diana is at that time the only one child in the entire Khmelnytska oblast that was unlucky enough to suffer from this disease.

Parents still can not believe that their child is sick because it is growing, gaining weight, develops as she should, laugh, stretches her little hands to her mother, understands everything... But the bone marrow does won’t operate properly. Along of the disease came the horrors: the temperature of 39, hospitals, thousands of surveys, up to 15 hours on a drip. How to overcome this? How to help save the child?

Since her 2 months the girl is constantly fighting for her little life. Diana is now less than a year old. Each month she suffers, especially of the skin problems. But without any immunity, her body won’t fight these problems. Therefore she has to take immunoglobulin and antibiotic therapy. The pure creature should constantly take an expensive drug Granocyte, which stimulates the production of neutrophils.

Ludmila, Diana’s mother: "I can not convey to you the words that I thought and what felt that moment. My heart and soul torn apart, but I knew I must be strong, not cry, not scream. That moment when I was told the diagnosis, I realized that whatever it is difficult and hard, I never give up! My daughter will live! Period! Good people, help my daughter cope with the terrible disease, as she has every chance to live. She is so small, but has undergone such terrible trial, and that it still lies ahead - is unknown. But one thing I know for sure - my child will live, I believe in it! ".

The only salvation for Diana - a bone marrow transplantation from non-relative donors abroad. However, this procedure cost (search for treatment and non-relative donor transplantation, including HLA- typing) is enormously high for the family. Of course, they’ve tried hard and were able to collect a certain amount already, but it is - a drop in the ocean. The purpose of this project - to collect the remaining funds for the operation to save the child's life.

Name: Diana Choban, born 4/29/13

City: Khmelnitsky oblast., Khmelnitsky region., S.Ruzhychanka

Diagnosis: congenital neytropiniya, Kostman’s syndrome