Small Klym is a prisoner of a terrible disease. 2

Klym is 4.5 years old. For more than three years, Klym has been visiting the Institute of Pain Problems clinic for supportive therapy: metameric massage, speech therapy massage and injections. The boy has a rare genetic disease – Werdnig Hoffmann's spinal muscular atrophy.

At first glance, Klym is no different from other children, except that he cannot walk and stand. His legs are his "mom and dad", he asks them to take him on their arms, as if he is walking on his own. Klym speaks well, loves to collect Lego, draws and plays computer games. Parents give the baby massages every day. They bought the device called a verticalizer so that Klym understood how to stand upright. Once a month, the family pays for classes with a rehabilitation therapist, and also buys vitamins abroad to support Klym's body.

Of course, this is not a full-fledged treatment, but the parents support Klym with all their might while they have been waiting for full treatment. Unfortunately, the parents do not have enough funds for all this, so they are forced to ask for help from caring people.

Let's help this kid get treatment to the clinic together!