The gift of fate

A young single mother, for which the child is the gift of fortune, stumbleв with countless difficulties. Her long-awaited boy was born with movement and vision defects. And the worst is the unknown, because the doctors still can’t diagnose the final causes of all these diseases. From the first days of the birth the mother was constantly fighting for the life of her baby. The need of intensive care due to the fact that the presence of so many diseases is constantly accompanied by the appearance of some complications. She can’t cope with this without our help!

The baby from the first pregnancy that's complicated by preeclampsia II and III trimester, was prematurely born – with disabilities, because of what he's unable to know what the real childhood is. The boy is unable to move, to eat by his own. He can't look at the sunlight because of what during each durable walking mother forced him to wear tinted glasses. Diagnoses of the boy aren't final. Considering that he has a "bunch" of diseases, it is difficult to establish the basic cause. Condition accompanied by bouts of lack of reaction to external stimuls, head jerking, lethargy child retraction of the tongue, recurrent vomiting child anxiety, lack of dialing weight. That's why it's so necessary the boy to be diagnosed abroad in order to determine the final causes of all these illnesses. Mother of little Romchyk appeals to all concerned to help in fundraising for passing diagnostic package at a leading hospital in Turkey "Medipol".

Bringing a baby alone, she's just no one to expect for his help. Without external assistance the mother is unable to find the required amount. Every day of her boy' ilness is costs so much. Accumulated funds sufficient only to accommodation, food and essential medicines.

In his eyes the light of life is shining. His mother dreams that one day she'll see her little boy running around with other kids, playing ball. The possibility tj make of the diagnostic tests is the bright spark of hope for rescuing desperate mother's own baby.

 

Name: Roman V.Vakulynskyi, born 15/02/2013

Location: Lutsk

Diagnosis: сhronic nonspecific mesenteric lymphadenitis. Delay in statokinetic development; syndrome of vegeto-visceral dysfunction due to the hypoxic-ischemic central nervous system injury. Cerebral nanism. Transient lactase deficiency. 2nd stage hypotrophy (27% underweight). Congenital defect of the posterior segment due to intrauterine left eye uveitis; partial coloboma of the iris in the right eye