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.<\/p>\n
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.<\/p>","protected":false},"excerpt":{"rendered":"
Csaba was born on October 6, 2020, as a seemingly healthy baby. However, at the age of two months, he was noticed to be weak and had a drooping head, so he was taken to a neurologist, who initially attributed the symptoms to laziness. Later tests revealed that Csaba has SMA type 1, a genetic disease, which is a rare inherited muscular dystrophy. The family immediately consulted doctors and managed to get the child the necessary medication.<\/p>","protected":false},"author":1,"featured_media":1894,"comment_status":"closed","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[36],"tags":[],"class_list":["post-1891","post","type-post","status-publish","format-standard","has-post-thumbnail","hentry","category-kategoria-nelkuli-hu"],"yoast_head":"\n