8-year-old Katya was born with rare Tricher-Collins syndrome. This is a genetic disease caused by a mutation in a gene. Such as Katia are called “a child without a face”. The disease is manifested in multiple development deformities of the maxillofacial area. Katya endured a lot of surgeries and the next one is on the line, but the family has no more money. The girl dreams of a new face and a beautiful smile. But the problem is not only in appearance. To date, deformed facial bones complicate Katia's breathing, hearing, and vision. Plastic surgery will improve the appearance of Katya, and most importantly help to breathe, hear and see.
HEALTH, SOUTH (10 of 77)
203 419 768.96 UAH collected in category Health
689 287.63 UAH - скарбничка категорії Health
Little Hlib was born on April 29, 2009. He was born prematurely and immediately in a difficult condition got into a resuscitation department in Kherson. After prolonged treatment, the child showed hearing problems, was diagnosed with "Bilateral neurosensory hearing loss, deafness of 4 degrees". Mum and relatives of Glebchik did not expect such a diagnosis, because nobody in the family ever had such problems. This diagnosis collapsed from heaven to head, but it does not look like a blessing ... The family was in a situation in which they did not know how to act at all. How to bring up a child who does not him? How to talk to him? How to teach him to speak? Is not it necessary to do it at all?
Nadiia is a beautiful woman and a kind mother of three wonderful kids, her profession is a garment technologist and designer and she is also a real craft artist that creates beautiful handmade flowers. Nadiia had a loving husband, a good job, in a word, "gracious living". However, her life suddenly changed. In 2013, she got seriously ill. She got Neuromyelitis optica or Devic's syndrome, that is an injury of the central nervous system. Nadiia was paralyzed from the waist down; she turned into a person with a group 1 disability. Her husband left her… Nadiia’s mother takes care of her and her three children.
Georgii Basko is 11 years old, he is a robust and purposeful boy who strongly believes that one day he will surely get up from his wheelchair and walk as before… Georgii was born absolutely healthy; he grew and developed on a par with his peers. However, when the boy was 4, a disaster happened – he was knocked down by a car. The child got a heavy polytrauma, head injury, brain contusion and was comatose for 5 days. By incredible efforts, the doctors brought him back to life.
Vlad and Yaroslav are soul brothers and brothers in life challenges. The probability of getting broken DNA is only 25% for everyone; there are very few families having two children with cystic fibrosis. But Kuzovye brothers were among them. The family tries their best. But it is terribly difficult to provide everything for the treatment of one patient with a serious illness, and even more difficult for two. Mom Natalya kindly asks to purchase the equipment necessary to ensure the qualitative daily treatment for the boys. Help today so they can live tomorrow.
Liza is so joyful, full of enthusiasm and dreams. It is weird to write about her on the page raising money for serious disease treatment... Drawing, children's fitness, bicycle, and rollers. She likes to visit children's entertainment centers, to help her grandmother and grandfather in the household. It's all about her. Procedures in the morning and in the evening, taking a lot of pills, special food, and special exercises every day during all her life is also about her, about Liza. The girl was born with a serious genetic disease and she needs help to live.
Now Misha Bilyi is 6.5 years old; he is in no way different from his equals in an age in appearance and physically, but he is lagging far behind them in his psychoverbal development. The boy hardly perceives the speech addressed to him; his active vocabulary corresponds to the age of 3 years. He goes to kindergarten with his twin sister; he eats by himself, but does it badly; his teachers help him to get dressed. He participates in matinees, although he never recites poems, in common dances he tries to imitate. When he was 2.5 years old, Misha was diagnosed with sensory alalia; the presence of an arachnoid cyst in the brain was revealed; the child understood or said nothing.
Tiny Angelina – the lesser of twins, during childbirth the girl suffered 2 strokes, oxygen starvation, whom, after which she had a brain hemorrhage. Doctors fought for the life of the baby, not departing from her for a minute. And Angelina survived!
It is the seventh time when little Tina's family seeks the assistance of UBB donors. Tina was born in hypoxia with the weight of 1100 g and spent 2.5 months in pathology unit of Odessa Regional Children's Hospital. For a long time, the child was fed through the tube only and got intensive medication. When Tina was five months old she was diagnosed with ICP and spastic quadriparesis. Tina is almost 9 years old now, but this little girl has already suffered a lot of pain and exhausting exercises.
"You are my soul...", said the tear-stained mom, sitting by the little Egor. And Yegor heard her, although he was in a coma... His condition was already stabilized, before that the boy had convulsions, his heart stopped. But he heard mom. For a whole month, the mother came to her son and said that she was near. The boy listened to her and once came to himself.
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