[ad_1]
Serbian President Aleksandar Vučić said the state is looking for someone to help treat Anika Manić, who suffers from spinal muscular atrophy and for whose therapy the citizens of Serbia are raising funds for therapy in various ways.
– We are seeing how to help the girl Anika Manić and Nikola Selaković spoke with Peter Sijart last night … Hungary will also help, we will also help transfer the little Anika to Hungary with some of the state planes before December 15 – said Vučić.
Anika’s parents raise money for the purchase of Zolgensma gene therapy, for treatment costs, as well as for travel and accommodation expenses.
Spinal muscular atrophy is a rare disease in which the body lacks a gene that makes a protein that motor neurons use for food. Since they have nothing to eat, these neurons, which transmit impulses to the muscles, die.
Responding to the question about treating children with SMS messages, Vučić said that this is how it is done in almost all countries, adding that he was proud that the state has been so committed to children with SMA.
Vučić added that the state fights for the lives of all children, noting that almost everything in our country’s health system is free.
[ad_2]
