What can only save Arina are hope and faith!
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The mother of three beautiful girls turned to us. Rykun Arina, the youngest daughter, was born on 10/01/2019. Within few minutes after childbirth, she was taken to the intensive care unit of the maternity hospital; her mother had not been allowed even looking at her and pressing the kid to her breast. A maternal intuition suggested that something was wrong. Every 3 hours Arina's mother came in to the intensive care unit and strained off milk little by little. “Is this not enough for her?” she worried then, not suspecting of difficulties yet to be encountered.
When she had been able to look at the child, her heart wrung with pain and what she saw."Don't cry, miss, she feels everything" the nurses said. But her mother had not heard their words, had not understood their arguments, couldn’t believe her eyes... Arinka has spent nine days at the hospital and all her nearest and dearest sat side by side grief-striken. They have obtained necessary medicine for the girl in the hope that their worries would be over and, having taken all those magic drugs, their daughter would definitely recover.
On the 10th day, the baby was moved to the intensive care unit of the children's regional hospital. She couldn't breathe herself. A little later, the mother has found out that her little girl had suffered sepsis, blood poisoning. On the 19th day of medical treatment, the child had a stroke and a heart attack, hemorrhages of the brain, the central nervous system damage and serious hypoxia, due to apnea (respiratory arrest). Mother and her daughter have spent 5 months in the hospital: 2 months in intensive care unit and 3 months in neonatology, all the time taking antibiotics.
Arina has the second type of hearing loss, she can hear therewith. Her eyes can’t see; ocular pressure is normal, but the child does not smile, does not focus his look, is unreactive to rattles and light. The doctors have assumed she has congenital glaucoma. It is no use crying over spilt milk. MRI of the baby’s brain showed a congenital anomaly and hypoplasia of the corpus callosum and cerebellar tonsils, microcephaly of the brain, tetraparesis. The doctors told that she won’t walk at all. But the girl's mother does not want to believe in this verdict. Arina continues enduring torments, daily droppers, injections, and replacement of catheters. It is hard even for an adult person to endure this, and the baby of 5 months sustained everything and couldn’t tell her mother how it hurts.
Now the kid is already 11 months old, she managed to complete 4 courses of exercise therapy and is preparing for the rehabilitation course and remedial gymnastics in Kiev. Arina does not hold her head up well, throws it back, does not focus her look, does not smile, can’t turn over, and so many “nots”.Only prompt actions can help her. Time and tide wait for no man and it works contrary to Arina’s state of health.
Her mother turns to everyone who is attracted to her little treasure and can give a helping shoulder in order she could receive treatment faster without wasting precious time!
Full name: | Rykun Aryna, 01.10.2019 |
City: | Makiivka, Donetzk region |
Diagnosis: | Tetraparesis, brain development anomaly |
ID: | 6385 |
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