Nika is 12 years old. He started 6th grade. Nika leads a perfectly normal teenage life: he plays online games, enjoys socializing with his friends and his elder brother, and spends much time on the internet. Nika takes a blogging and moviemaking course on Sundays. Actually, he doesn’t know yet what he wants to do when he grows up. Nika likes painting cartoon decorations, building Lego models, and sometimes helping his dad with cooking.
He has to write a lot in school that’s why he does arm exercises. They are necessary to maintain dexterity. In contrast to his peers, it’s physically harder for Nika to complete tasks—school assignments and game missions alike.
Nika has spinal muscular atrophy (SMA) type 2. It is the rare genetic disease which causes gradual muscle weakness and loss of movement. He cannot walk so he uses an electric wheelchair. Last year Nika started to take a medicine which slows down the development of his disease. Thanks to injections of the medicine and his usual practice, Nika has become stronger and more resilient.
Now Nika needs a new comfortable wheelchair to use at home because the old one has been in regular use for over 3 years.
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