6-YEAR-OLD VIKA HAS HIGH EPI-ACTIVITY. WITHOUT EXPENSIVE LABORATORY EXAMINATION IS IMPOSSIBLE EFFECTIVE TREATMENT!
The story of Vika and her parents is painfully touching.
Vikulya was born in Dnipro. Childbirth was difficult. The girl slept badly, and her mother padded all the thresholds of doctors. When she was 2 months old, doctors were horrified to notice that she had serious CNS problems.
It was said that the child is hopeless, does not hear, does not see, severe epilepsy, it is unknown how long she will live.
In order for the daughter to recover, the parents took turns working wherever they could find part-time work, not sleeping at night, working part-time at night.
At the same time, the young family has difficulties with housing. Relatives were illegally sold their parents' apartment, and the family is moving to Zaporizhia. Vika's up to 3 years was in the hospital: seizures, infections, any stimuli dangerous to the child's life.
Vika's mother, Tanya, was torn between two hospitals. Her father had cancer. And when Vika was 2 years old, her grandfather died.
It is difficult to imagine what huge sums the family spent in that period! And how difficult it was for them morally...
Now all doctors are shocked that Vikulya is alive, that she is 6 years old, she holds her head, watches with her eyes, sits in a wheelchair, turns over. Her parents won her life! And now they are not going to back down. The question is money. During all these years, the family is exhausted both morally and financially. The head turns from thoughts about money, about expensive rehabilitations and medicines.
Today Vikulya needs an important examination. Doctors insist on passing a special genetic test, which is sent to a foreign laboratory. This analysis will help identify the cause of high epi-activity. Without it, doctors will not be able to prescribe a full and effective treatment.
Good and sincere Vika sees and understands everything. She reaches out to children, wants to be friends with them. Let's support the family, help Vikulya reduce epi-activity and become healthier!
Name: Chetvertak Victoria
Date of birth: 22.04.2015
Diagnosis: Congenital malformation of the brain. Symptomatic epilepsy. Partial atrophy of the DZN of both eyes
The purpose of the project: to collect UAH 19,500 to pay for laboratory tests at the 'Mama Papa' Medical Genetics Center
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