Muhammad is 5 months old, the child's health problems were detected immediately, from the first days of life. After a month spent in hospital, the mother and baby were discharged and the boy's condition was assessed as satisfactory.
Unfortunately, within two months the yellowness of the skin increased and the child's sclera became sluggish and restless. The tests were poor, bilirubin was very elevated.
The family sounded anxious. Doctors at the Republican Hospital sent the child's medical history to Moscow. A week later, Muhammad and his mother were summoned to the NIIC of Children's Health of the Russian Health Ministry for hospitalization, to clarify the diagnosis and determine the treatment method.
The child was thoroughly examined, and doctors found a serious pathology of the boy's biliary tract, as well as signs of beginning cirrhosis of the liver.
In order to determine the cause of the disease, Muhammad urgently needs a genetic analysis to confirm the diagnosis and understand the treatment required for the child. However, at the expense of the OMS, such tests are not carried out. Molecular genetic tests are paid for and often very expensive.
The condition of the child may deteriorate at any time, so no time should be wasted. Delay in providing assistance may lead to irreversible consequences.
The young family is in a difficult financial situation. The income of the family does not allow for urgent collection of the necessary amount and analysis.
At present, Muhammad and his mother are hospitalized at the NIIC of Children's Health of the Russian Ministry of Health on supportive therapy.
Muhammad's parents need your help!
