Small, unruly arms and legs, a kind face and the depths of the ocean in her eyes… It’s impossible to pass by Katja and not inquire about her fate, not smile back. But when you realize that this child has got into trouble, the smile fades away. Katia struggles for her health, for small steps on the road to recovery from birth.
HEALTH, EAST (10 of 104)
194 356 764.31 UAH collected in category Health
256 578.56 UAH - скарбничка категорії Health
Vania got diabetes when he was 5 years old. He had great thirst, then prolonged vomiting. Doctors treated the poisoning, but the kid quickly lost weight and weakened. After a full examination, Vania was diagnosed with diabetes. Since there is no children's endocrinologist in his small town, his mother had to take the child to OKHMATDYT. There, Vania was helped a lot: they removed acetone from the body, picked up insulin doses.
Recognizing the diagnosis is the path to this is long and difficult if we are talking about orphan (a rare) disease. Without a diagnosis, it is impossible to prescribe a treatment that will deal not only with the symptoms but with the cause of the disease. For 7 years, doctors have not been able to determine what is the root of the ills of 7-year-old Andrii: developmental delays, problems with blood vessels, joints, and heart. To confirm the diagnosis, you need an expensive laboratory test in Germany.
Denys is 7 years old, this is the time when mothers take their children to the first grade. And every morning Denys’s mother takes her son to classes with a psychologist, a pathologist, a speech therapist. Severe metabolic disorders, organic damage to the central nervous system – indifferent medical terms are recalled from my mother in the soul by the verdict of an unknown judge. Contrary to all diagnoses, Denyska is growing and developing, but in addition to training with specialists, he also needs expensive medicines. Now Denys needs our help with you to take a course of Cerebrocurin.
Some children are destined to be born immediately in adults. They should immediately challenge the right to life, fight for it and fight daily for their health. Maxym is just like that. Although he is still quite small, in his 6 years he has survived so much that not every adult will survive.
Surely many people remember Zhenia Mikulich: cute brown-eyed boy from Donetsk region. Several years ago, thanks to the support of caring people, this boy received the necessary medicament for treatments a fungal infection of the lungs. Zhenia was sick from the first month of birth. In the first years of his life, the boy suffered soft tissue infections (paraproctitis, panaritium), inguinal and cervical lymphadenitis, hypochromic anemia from 9 months, secondary cardiopathy, and follicular angina. Not to mention pneumonia and lymphadenitis... And only some time later, after a detailed clinical examination, the cause of Zhenia's frequent illnesses was established. The boy has primary immunodeficiency, chronic granulomatous disease.
Three years ago, having withstood all the upheavals, Ilya Titarenko survived. This was the beginning of the boy’s life, each day of which is more like a struggle than happy and carefree childhood. In the achievements of Illia, there is still too much “not”: he does not sit, crawl, walk or speak. But he understands everything, and the whole range of emotions is reflected in Ilyusha’s little face and in brilliant eyes. The preservation of the intellect makes it possible to further develop successfully. Here are just the financial costs of a family where there is a child with special needs, are incommensurable with income. We can give this little man the opportunity to fight for his health, which the disease has so mercilessly stolen!
This little sun with the gentle name Olesia was born on January 1, 2015. The girl has cerebral palsy, and this diagnosis is not so bad when she has severe epilepsy and 6 operations on the gastrointestinal tract behind her back. In any case, the brave Olesya together with her parents overcame all this, and now her main task is effective rehabilitation. Now is the time for her, the brain is most susceptible to learning. To make new steps in development, the baby needs your help.
This story is about despair, hope, and miracle. At first, there was a long and difficult path to the two long-awaited strips on the test. And the state of unreal boundless happiness of parents-to-be. And a complete unawareness of what fate has prepared for them. The first alarm bell appeared at 19 weeks, the threat of interruption chained mother until the end of the pregnancy to the hospital bed in the pathology department. It was difficult and disturbing, but she was warmed by the thoughts that everything would end soon, a son would be born, and everything would be fine, and at home, everything would be forgotten like a bad dream.
"I’ve been putting off this letter, I wanted to give the opportunity to other kids to get help faster. My Irishka lives with cystic fibrosis. Our inhaler broke down with no chance to fix it, but without inhalations, she can’t live a single day... Can you help us?", Iryna's mom writes. We have known Irishka almost since her birth, and now she is preparing for school. She lives together with her mother, dad helps only partly. "Sometimes I fall down. I am a strong woman, but when it comes to my child... sometimes I panic. When there is support from the outside, it touches strongly and raises the spirit".
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