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Sofija Markuljević, one year old, who united the human people of Serbia, arrived in Los Angeles for treatment on August 23, and has now received medication for Zolgensmu.
“Our dream has finally come true. Everything we have fought for together in recent months has paid off. Thanks to all who were part of our fight and thank you for continuing to be with us,” they wrote in Twitter Sophia’s parents.
As the parents of little Sofia announced, The girl is expected to remain in the United States for three to four months..
Sofija Markuljević was born a healthy child, with a high note of nine. During the first month of her life, she looked like all healthy babies, but in the second month, Sofia stopped moving her arms completely.
At two and a half months, it was determined to be a rare, but extremely progressive and fatal neuromuscular disease: type 1 spinal muscular atrophy.
The cure for this disease is the most expensive in the world – it costs a staggering $ 2,100,000 and is registered in the United States alone.
For months, Serbia has been raising money for Sofia’s treatment and numerous celebrities, businesses and the media have been involved. The first victory was lost: On July 30, the Markuljevic announced that the money had been raised.
