Csaba was born on October 6, 2020, as a seemingly healthy baby. However, at the age of two months, weakness and a drooping head were noticed, so he was taken to a neurologist, who at first attributed the symptoms to laziness. Later tests revealed that Csaba lives with SMA type 1, a genetic disease, which is a rare inherited muscular atrophy disease. The family immediately consulted doctors and managed to get the child the necessary medications. First, he received a treatment called Spinraza, and then, at the age of 9 months, the Zolgensma gene therapy, which was funded by the state.
Csaba's development is supported by intensive physiotherapy and hydrotherapy, as well as special kindergarten support. He has already learned to sit, roll over, talk and stand holding on for a short time, but he still has a long way to go before he can take independent steps. The family supports his development with love and commitment.