In 2012, the Prelovskys' family experienced great sorrow - a child died. Four years later, Anechka was born. Happiness entered the house again. Nothing foretold trouble. The girl grew and developed as all children, but at about a year old she began to bleed frequently from the nose, under the eyes appeared bruised, teeth began to crumble. Doctors in Irkutsk attributed all problems to a lack of micronutrients in the body. Once at the doctor's appointment, he found out that the child's liver was enlarged. The biopsy results showed a terrible diagnosis: "cirrhosis". After the examination we found out the cause - Anya has a rare hereditary disease - Tyrosinemia. Usually timely treatment helps to prevent serious complications caused by the disease. But time was missed, the baby's liver was already damaged and she had to have a transplant. More than four years have passed since the surgery, but Anna's condition is still dangerous for doctors and parents. The child literally "does not get out" of hospitals. She has to fight gastrointestinal, pulmonary, neurological and bone fragility problems at the same time. Parents do everything possible to help their child: Anja's father regularly takes her to physical training, and her mother dedicates all her energy to her daughter's intellectual development. But the most important thing for Anja is, of course, the careful medical control of the transplanted organ and the use of medicines and a special diet with low protein content. All medications are given to the child free of charge at his place of residence. But the family cannot afford to buy tickets for trips from Irkutsk to Moscow to the Shumakov Center and expensive medication. This is why Anna's parents asked a charitable foundation for help.
Verified by Tooba
Verified by Tooba
