
© Familia de Isabella
Isabella's life is still at risk, because to ensure the successful result of a liver transplant, she needs very expensive medicines that her family can't pay for without government support. Venezuela, in turn, is not able to pay for her treatment because its funds are blocked in the United States.
Esther Yáñez Illescas - Isabella lives not knowing that her life depends on coloured pills. She is 21 months old, and her speech is clear only to those who look after her on a daily basis in the Italian hospital of Buenos Aires, deciding which pill she needs to take.
Isabella was born with a congenital disease and doctors immediately warned that she required a liver transplant to survive. Her parents, Douglas and Yelibeth, addressed the issue straight away: donor, funding, where, how and when the transplant will be performed.
It wasn't so difficult. Yelibeth was a match and could be her daughter's donor, and all the treatment was covered by the Simon Bolivar Foundation, a charity funded by the US subsidiary of Venezuela's state-run oil company PDVSA - Citgo.
The agreement between the Italian Hospital of Argentina and Venezuela has been in force since 2007, and 109 Venezuelan children have undergone organ transplants under this programme during this period. High-skilled specialists of the Italian hospital have been conducting transplantation surgeries for 12 years.
Douglas and Yelibeth left everything behind in Venezuela and in September 2018, without worrying about the political situation in the country, moved to the capital of Argentina. Their eldest son Abraham, who's 12 years old, went to school in Buenos Aires.
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