Total raised
BYN 4 342,61
Total raised (%)
100%
Meet the child
Stanislav suffers from a rare genetic condition. Symptoms started appearing at the age of 6 and included headaches and vomiting attacks. There was a need for hospitalization. In the future, headaches will be combined with abdominal pain. Numerous studies have been performed that have revealed signs of demyelinating disease and metabolic disorders in the spectrum of organic aciduria. Complete exome sequencing is the recommended way to clarify the diagnosis.
