Already in two years Albina's kidneys failed due to genetic disease - hemalytic uremic syndrome. Now Albina lives thanks to a daily procedure of peritoneal dialysis: in the abdominal cavity there is a catheter, through which the medical device pumps, and then pumps out a special solution. At the same time, this solution removes not only the toxins, which should have been removed by the kidneys, but also all the necessary substances. It is impossible to live on dialysis for a long time. Albina needs kidney transplantation.
According to doctors, the operation should have been performed on a girl long time ago. Albina was prepared for her, all the tests and preoperative vaccination were carried out, which was very difficult to do in conditions of covide spread. They even brought her to Moscow from Vladivostok. But such little children were not taken for a transplant according to a standard treatment protocol, and the child would not be able to grow up and gain weight without kidneys.
Albina can be saved by transplantation using an international protocol, but only surgery is free of charge, but the drug used in its framework Alemtuzumab is not part of the Russian standards of treatment and his family can not get. Although it is the drug that ensures the survival of the donor organ and helps the young child to survive the surgery.
Parents have no money - one bottle of the drug costs 277,965 rubles, and three bottles are needed to take Albina to the surgery. Mom gives her kidney to her daughter.
We will help to pay for the medicine!
