natalya kravtsova turned upside down when her two-year-old daughter was one year and 4 months old; little vika was diagnosed with a rare genetic disease. spinal-muscular trophy. the second, like a couple of days ago, the child was injected with the drug zol, gensma pregnancy, everything was going well. and here we are a year old we celebrated vikulya, too, everything was fine, but over time i began to notice that she was losing our skills and, as if at first, no matter how much she betrayed this meaning. well , you never know, the kids administered this drug to two more boys at the same time. everything is now under the supervision of doctors so that the body does not reject the medicine for the first eight days. an hour closely in the department about intravenously , the procedure is far from simple, therefore, in general , specialists have been trained in this therapy , it is on and with the maximum probability it will be give an effect in cases where spinal muscular atrophy is not yet strongly manifested. that is, in the child’s spinal cord there is still a preserved part of the cells