Maryam was born at 42 weeks. Health problems began immediately after birth, as she had hypoxia. They carried out the necessary treatment and a month later she was discharged from the hospital. After a while, the parents began to notice that the child gets tired quickly, constantly sleeps and does not cry and immediately sounded the alarm.
In the fourth month, the parents decided to go to Moscow for an examination. And there they were diagnosed with grade 2 dystrophy, acute infection. They began to treat and further examine. They passed tests to a geneticist, and
were diagnosed with deletion of chromosome 13, partial monosomy.
Maryam didn't know how to do anything, her muscles didn't work, even the muscles of her stomach and mouth. After the treatment began, she began to eat, cry, laugh. And contrary to all the doctors' predictions, Maryam began to walk, but she cannot climb, descend and jump in her 4.5 years. This fragile and sweet girl is very diligent and strong.
In order to maintain and develop the muscles of the body, she needs to be constantly engaged. Parents are doing their best, but they do not have enough money to pay for continuous rehabilitation.
Let's support and help Maryam undergo rehabilitation together!
Дорогие друзья 🫶🏻осталось совсем чуть-чуть! Давайте поможем закрыть сбор для Марьям.
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