4-YEAR-OLD DENIS WITH A GENETIC MUTATION IS WAITING FOR TREATMENT! HELP THE BOY!
The number of diagnoses that our little ward Denis Puzan is facing is amazing. He has a defect in the development of the cerebral cortex, epileptic encephalopathy, vision problems, an anomaly of the musculoskeletal system of the whole body, joint weakness, hypotonia, difficulties with feeding and metabolism, growth retardation, underweight.
At the age of three months, the baby was diagnosed with ischemic damage to the central nervous system and neuromuscular syndrome. Denis almost did not move, could not eat on his own, slept constantly. When he was 2.5 years old, lab tests in the US revealed that the boy had Chu-Tokit-Takenuchi-Kim orphan syndrome, caused by a genetic mutation.
Despite the disappointing forecasts, the parents did not give up. Tireless work, regular rehabilitation measures contributed to positive changes. Denis has improved muscle tone and fine motor skills. Now Denis should continue to work on improving coordination of movements and concentration of attention.
In order to acquire new skills, Denys needs rehabilitation courses that cannot be missed in order to consolidate the result. Please help the family pay for scheduled classes this October!
Full name: Denis Oleksandrovych Puzan
Date of birth: 15.05.2018
Diagnosis: Chu-Tokit-Takenuchi-Kim syndrome. Epileptic encephalopathy in the stage of drug remission. Myopathic syndrome. Delay in psycho-speech development
The goal of the project: to collect UAH 20,000 to pay for a rehabilitation course at the Victoria Child Rehabilitation Center
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