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Important: Important information
Diagnosis: Protein-energy deficiency, severe, bilateral deafness, grade 4, mild hypermetropia of both eyes, horizontal nystagmus, delayed statokinetic and psychomotor development with pre- and prenatal hypo-esic-ischemic lesions. Central nervous system, affective and respiratory attacks, muscle hypertension syndrome
History and appeal from the words of the mother:
“Olivia was born prematurely on 02/24/2022 weighing 1120 grams, the second of triplets, a month after birth she was evacuated to the National Children's Hospital “Okhmatdyt”, the child was admitted to the department in serious condition, after a month of treatment she was discharged home, but later the child was diagnosed with developmental delay and deafness.
The child is infected in its 2nd year, do not sit, do not walk, weigh 8 kg, after proper examination, it is recommended to undergo genetic testing, for which it is necessary to perform a large number of tests, after which it is possible We will hold a bath so that Olivia can quickly catch up with her sisters and be able to live a normal life! ”
At the moment, it is necessary to carry out genetic laboratory research for a total amount of 15,995 UAH.
LET'S CREATE GOOD TOGETHER!!!
The child’s documents are hidden to protect personal data and to keep them from fraudsters who profit from other people’s misfortune. Documents are provided to patrons and donors on official request.
Code 39333086, MFO 305299
Code 21133352, MFO 322001
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Diagnosis: CEREBRAL PALSY / ASD
Learn more: Let's give hope to 74 children with disabilities TOGETHER

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Diagnosis: ДЦП, спастичний тетрапарез, симптоматична епілепсія, ЗПМР.