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The money needed to treat Oliver Pal Gajodi from Bajmok was raised, Oliver’s father Jožef Pal confirmed for RTS. An exam is scheduled for January 25 at the Budapest hospital.
Oliver is a one-year-old boy from Bajmok, near Subotica, who suffers from a rare and serious disease: spinal muscular atrophy. It is necessary to allocate about 2.3 million euros for an effective individual therapy for this disease.
It is a very progressive disease that attacks the muscles and the basic functions of life, such as walking, digesting, swallowing and breathing, are quickly lost.
Oliver is currently at his home in Bajmok, and an exam is scheduled for January 25 at the Budapest hospital, where doctors will prepare him for expensive gene therapy with the drug “Zolgensma”, which should stop the disease, he reports. RTS.
“According to our budget, we collected the amount of ‘zolgensma’, but only on Monday we will receive an official notification from the bank,” says “On Oliver’s life” on Instagram.
“It is important to know that the excess money raised that is needed for the ‘zolgensma’ can only be used for ancillary devices and therapies that Oliver needs after gene therapy,” the announcement states.
Oliver should receive the precious medicine until his second birthday, but every day before is important for his recovery and physical development. That is why humanitarian bazaars have been organized throughout the country.
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