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Nicholas was born as a rare condition in which his arms did not develop properly (Photo: Playback: Gofundme)
Since he was born, little Nicholas, 2 years old, from Dallas, Texas (USA), has faced a great challenge. Because he has a rare genetic disease, he was born without knee joints and his arms did not develop properly, so his hands appear to be directly connected to the trunk. Without the knee joints, Nicholas cannot walk either. However, this reality may change in the coming months. According to the newspaper Meter, the boy will undergo pioneering surgery in Florida in August, which should allow him to walk. To carry out the procedure, the parents of Nicholas, Christina and Cristopher Cabal, must pay between US $ 20 thousand (R $ 111 thousand) and US $ 30 thousand (R $ 167 thousand).
A LIFE OF ADAPTATIONS
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Nicholas was born in October 2017, with a condition known as thrombocytopenia syndrome, which affects bone development. The mother says that she had heard of the disease, but did not imagine that her son would have such serious problems. The syndrome also affects blood cells, so patients are at high risk for bleeding and require regular blood transfusions.
Christina, who has another 3-year-old son, said it was difficult to adjust to caring for a baby with such complex needs. To help Nicholas move, he underwent medical treatment to learn how to move and eat. The house also needed to be adapted to provide security for Christina’s son.
For fun and movement, Nicholas plays on his tablet. Also, after treatment, the boy made great progress and can now use silverware and even pick up items. According to his mother, he can live a happy life like any other 2-year-old, but she believes that her son would have a better quality of life if he could walk, especially as he grows up.
Parents are optimistic about the surgery and hope that their son can take his first steps in 2021. For this dream to come true, they will spend six months in Florida (USA) and Nicholas will need a lot of therapy to learn to walk.
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