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For the brave child Oliver, a one-year-old from Bajmo, who made people from all over Serbia, Hungary, Bosnia and Herzegovina and many other countries come together and show how noble they are, enough money has been raised for Zolgensma, the world’s most expensive drug that cures deadly spinal muscle. atrophy.
The fundraising action for Oliver Pal Gajodi was carried out on the Internet, then with the help of humanitarian bazaars, by sending SMS messages, various games and in all other ways that contributed to the raising of money. When the parents found out that the goal had been reached, Timea Gajodi’s mother cried, while her father, Jožef Pal, said in disbelief that he couldn’t believe what he was hearing. Although since the beginning of this year, when they found out that their newborn son was suffering from SMA, they believed the day would come, it is amazing for the family that they managed to contribute money and for that they are very grateful to the army of people who supported them. .
At the head of that army are several women who are part of the great support to Oliver and the Pal Gajodi family.
– Everyone must have heard that the money needed for Oliver’s treatment was collected last weekend. The action took place internationally. Now we can say with certainty that it was a success, it was said at the press conference held in Subotica.
Zolna Gajdoš Bajus confirms that little Oliver arrived in time to raise money for therapy that will significantly facilitate his life and improve his condition.
– Oliver will travel to Budapest on January 25, where he will first be separated from the respiratory system. After that, you can receive Zolgensma, which means that you will receive the bill for the drug only at the end of the month the money will be paid. This is not the end of the fight, Oliver will continue to need money and will continue to be present at the Be Humane Foundation as he will need money for rehabilitation, spa, physiotherapy, various resources to help him develop … says Gajduš Bajus.
Livia Abraham is one of the administrators of the “Facebook” group, founded in July, which has gathered 27,000 members to date.
– The atmosphere in the group was very good, we had good auctions. In September alone, one of the administrators established 200 offers. We had a bike auction, the owner was from Ada and he drove the bike to Senta himself, but we also had auctions from Budapest. There were days when I worked in groups for seven or eight hours, but in December it was already much easier because we had a large and well-coordinated team. I must also mention the last auction, it is a book by Daniel Varo. We finished it at midnight and managed to bid up to 17,000 dinars – says Abraham.
Silvia Feher recalled that the humanitarian bazaar was started by a mother of three girls who sold lemonade at the market with children in Bačka Topola.
– Then other people started selling lemonade, cookies and much more. A grandmother gave 10 dinars and asked if it was enough. Of course, each dinar was equally important. Similar actions took place everywhere in Vojvodina, throughout Serbia. For Children’s Week, we asked the children to choose the toys to put up for auction. We organized a virtual birthday of Oliver, we also baked a virtual cake – said Silvia Feher and recalled that the SMS games in the group were launched in August.
– There were mobile phones, a dollhouse and the car was the most important thing we got for the SMS game.
The team that was and remains with the Pal Gajodi family and the starry-eyed boy, little Oliver, expressed a big thank you to everyone who helped in any way and contributed to raising money in record time.
– When he goes to Budapest, Oliver will do the tests and then the family will receive a pro forma invoice. After payment, the drug will arrive from America to Budapest. This is followed by gene therapy, followed by three months of steroid therapy and rehabilitation. In Budapest, more than a year ago, the first child received gene therapy. The mother of that child, who is a year older than Oliver, announced about three weeks ago that the child was walking. So far, nine children have received Zolgensma in the same hospital and are expecting little Anika in the same hospital this month, members of little Oliver’s support team said.
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