Mykyta and Glib are twins, and all of their 5 years of life struggling with cerebral palsy. Earlier, the boys were engaged in rehabilitation by the method Vojto-therapy in the Czech Republic, they are now undergoing rehabilitation in the Ukraine, in the Center for physical rehabilitation "Step by Step". The boys held through a lot, but treatment should continue.
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Danya has neyrosarkoma - a malignant tumor on the leg. Treatment in Ukraine hasn’t brought any positive results. Doctors offered two-year child amputation of the leg – in our country there is no possibility to undertake something to prevent metastasis. During the examination in Turkey, local doctors saw an opportunity to save not only his life but also the leg. This requires a complicated operation and chemotherapy. Cost of services in Turkish hospital is 30,000 dollars.
Yehor was born in June 2009. And already from the first minutes of his life, everything was not right. The lungs of the child did not fully open, began the hemorrhage in the brain. Doctors make a serious diagnosis – internal hydrocephalus – it is a complex disease when the child's brain accumulates excess spinal fluid, which must be forced out through a special shunt.
Sukhoruchenko Mykhailo was born on September 8, 2009. He was born without skin on the right leg, the so-called "socks effect", that is mean that skin was not exactly along the perimeter of the toe. Misha's mother immediately realized that this is a terrible disease, which took away her first son, who lived only 2 weeks. Mom knew one thing, that none of the doctors know anything about this disease. She was told that they were the first, and if anyone was born with this disease – no one survived, and indeed, there were no records of such patients in the state, but that did not mean that they were not!
Mother's son, mother’s joy – Zhenіa. He is seriously interested in cars, likes to dance and sing together with his brother and to read books with his mom. "I call him sunshine because he always smiles that way," says mother Olga. Zhenшa is smart and playful, and a serious illness prevents him from living as actively as he wants. He has to spend a lot of time on daily procedures. Also, the baby is gaining weight poorly, is not developing well, because the family is not able to provide everything necessary for treatment – it is too expensive. However, if we help to buy good-quality medical equipment, supplies, and nutrition, Zhenіa will have more time and strength to live the usual life of a young boy.
Rustam is 16 years old. Throughout his life, Rustam suffers severe pain. Every day for several hours goes on unbearable dressings. Rustam is a baby butterfly. His diagnosis is bullous epidermolysis. The boy's skin is so fragile that even mom's caress can harm him!
Rustam was born with a shocking rare diagnosis. Neither parents nor doctors were sure whether a boy would survive. No one gave a guarantee that a child would live up to 2 years old.
The mother of two charming infants turns to all caring people with a request to save her babies. Diana and Mykhailo appeared with the help of the C-section. Unfortunately, the two angels were born prematurely, with underweighting. They were connected to the reviving apparatus for two months. Finally, the children went on the next stage of treatment. They grow up, gain weight and parents are happy. After 109 days, brother and sister were discharged from the hospital. Before being discharged, they were vaccinated against hepatitis B and BCG.
It is difficult to survive the betrayal of a loved one. Moreover, when you are not able to stand up for yourself... Little Ira now lives in a new family, she loves and cares about her very much, she has two foster brothers. And the biological mother left the girl when she was only a week old. The woman left her daughter in the dental clinic and just left.
"We really need your help", Julia, the girls' mother, writes in her email to us. For the last 15 years, the most important thing in her life has been fighting for her two daughters. Sisters Lera and Sasha were born with a serious genetic disorder. To keep this disease in check and not to let it destroy one's body, one needs a great deal of effort, work, and money. Some of the medically necessary things are paid for by the government medical programs, some of them Julia pays for, but it is impossible to afford everything without the help of caring people. When one child is seriously ill, it is a difficult situation; when both children are seriously ill, the situation is twice as difficult. Please help us support this family.
We convey words of gratitude from Eva's parents to everyone who helped the girl with the first operation. The eye has been successfully operated on, and the joys of parents have no boundaries! "The positive results were already at the first examination of a specialist," says the father of Eva. "We heard the long-awaited: vision has improved! And the daughter’s words that the eye began to see better give hope that she will have a long-awaited good vision".
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