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.
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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?
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.
The girl lives in Odessa, she is 19 years old. She has severe thoracic scoliosis, a hump grows, curved ribs squeeze the heart and lungs. The angle of spinal deformity is rapidly progressing and has already reached 52 degrees. The only way to straighten the girl's back and relieve her from excruciating pain is to perform an operation on the spine with the installation of a fixing metal structure. The University Hospital of the Kharkiv National Institute of Pathology of the Spine and Joints named after M.I. Sitenko is ready to do such an operation for Alina, but the operation is very expensive.