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The whole nation learned of the true Serbian hero, Miloš Mijailović from Gornji Milanovac, overnight.
This young man, together with his sister Biljana Dragicevic, started an interesting auction of a house in Rudnik, as a kind of contribution to the action already started to raise more than two million euros for the treatment of little Anika Manic abroad to through the humanitarian organization Be Human.
They started with a price of 4,000 euros, but that amount was quickly exceeded.
“The auction lasted until November 18 until 8 pm, and on the first day the man from America who made the largest offer, almost double the initial one, appeared. This house and this move pushed some things. other people, like a chain reaction, so I don’t think it’s just that $ 8,000 in question, but that’s the beginning of what was paid for, “Milos told Kurir television.
He added that the most wonderful thing Mr. Spasoje from America has in mind is to renovate the house afterwards and give it to Anika when she recovers and turns 18.
Milos also invested his expensive motorcycle vest in the recovery of Anika, whose value he estimated at 3,000 euros.
He says there is not enough money yet, they are only 70% of the total amount, and the time is getting shorter.
Let us remind you that two-year-old Anika Manić was born a healthy baby. A few weeks later, at the doctor’s regular check-up, something was wrong. His reflexes slowed. After detailed examinations, the diagnosis of spinal muscular atrophy came. In translation, his muscles are slowly failing, and for treatment in early January in Hungary, he needs the most expensive drug in the world, which can be accepted up to a certain age and weight of the child.
The mother of little Anika (2), Ivanka Manić, thanked all her friends, relatives and human persons who have been participating in the action to collect material aid for innovative gene therapy abroad of 2.1 million euros in recent months.
For Kurir television, he revealed where Anika is currently, what is her state of health and how long she has left to buy the most expensive medicine in the world, which she should receive in Hungary.
We still need about 500,000 euros and we only have three weeks left. We would think that it is impossible if we have not already raised 1.5 million euros. And we hope that Anika lives for us because we see that her condition worsens, she breathes with more difficulty and swallows. “The support of good people is now our whole world!” Said the mother of a girl who suffers from type 1 spinal muscular atrophy, that is, muscular atrophy and inability to perform basic vital functions: breathing, swallowing and moving from independently.
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