Total raised
BYN 4 349,30
Total raised (%)
100%
![Valeriy Karachun](/upload/resize_cache/iblock/173/6tv2lgx6cyn4fatzeupgxwenwi5htsm8/375_375_1/IMG_d01527bf9bb67ea56b55c8259394c219_V.jpg)
Meet the child
Little Valeriy is worried about bouts of weakness in one side of the body, sometimes in all limbs, lasting several days. These attacks occur twice a month. The first symptoms appeared before one year of life. According to the clinical picture, doctors believe that alternating hemiplegia is a genetic condition. The treatment for this disease is specific. To confirm the diagnosis the child needs a genetic study - complete sequencing of the CeGat exam. Valeriy was supported by «Chance» program.