Zhenia is only two years old. This baby has a congenital cataract of the right eye and he needs an operation to replace the lens. this diagnos was put to the baby at birth. Then, in the maternity hospital, it was recommended to the mother to drop eyes of her son’s eyes and observe. But, unfortunately, the drops did not give the expected result. Mom herself already saw a white spot on her son’s eye. And at the next visit to the clinic, Zhenia revealed cataract progression. To save eyesight on the right eye, the baby needs to have an ophthalmic surgery.
252 533 543 UAH
HEALTH, EAST (10 of 108)
676 804.34 UAH - reserve fund Health
Infections are not pleasant to anyone, especially their complications, and for our patients, they carry an extremely serious threat. From birth, our boys and girls have been living with a serious illness that affects the respiratory system. They are especially vulnerable to infections. Even when a simple ARVI lasts a long time and has complications, surviving the flu or pneumococci is a test that is better to avoid at all.
St. Nicholas Day is a celebration of mercy, warmth, joy, kindness, and love. I want to believe that it will remain forever in the memory of little children, and, perhaps, when they want to help those in need. Good deeds are always relevant, and they acquire their characteristics and charm on the eve of Christmas and New Year holidays. Our dear benefactors, helpers, like-minded people, and caring people, we turn to you for help for 10 families raising children with terrible diseases (cerebral palsy, Down syndrome, cancer, orphan patients). Left alone with their problems, such families spend a lot of resources, effort, and finances on the treatment and maintenance of the life of their seriously ill children.
Dreams should come true! Parents of a special baby ask to help their little Polina, who needs to undergo a very important rehabilitation course! Polina is special not because she has a cerebral palsy, but because this girl is stronger than many adults. During the 5 years of her life through hard work and pain, she already achieved a lot. She seats by herself tries to talk. Despite the disease, she is a cheerful girl, who wants to move. Everyone who knows Polina notes how much she wants to run and dance! But unfortunately her hands do not work well, she can’t concentrate, all the skills which are easily mastered by other kids, Polina needs to learn hard.
No one knew if Vika would survive. After a premature birth, the girl did not eat, she stopped breathing, so she was in intensive care. Then she was diagnosed with cerebral palsy and Dandy-Walker syndrome. But Vika survived. Although she now has to challenge the right to every free movement, she is alive! And she pleases her relatives with new skills that are given to her with such difficulty...
Everyone who meets Dasha involuntarily compares her with a small, energetic puppy. The baby has a lot of energy and positive. She loves animals and it seems that they all feel it, because they run to her from all sides. Dasha can’t sit still for a minute. As soon as she stops for a few moments, she immediately manages to do mischief, with the words: "I could not help myself, I was bored!". Parents are still happy for such activity because, for children with cystic fibrosis, movement is life. And for Dashuli, it’s doubly, since she has had a destructive Pseudomonas aeruginosa in her lungs for several years.
Pavlik is only 5 years old, and he already has a bunch of terrible diagnoses: cerebral palsy, symptomatic epilepsy with attacks. The boy needs help in acquiring a device that is very necessary for him – orthoses for legs, worth 12,180 UAH. This will prevent surgical intervention and improve the quality of his life. Parents made bright plans for their boy, but it happened as it happened. Preterm birth at the 30th week of pregnancy because of placental abruption, a long stay in intensive care, coma, mechanical ventilation. Doctors did not give any chance that the child could survive, but a miracle happened.
In the 35th week with severe hypoxia, Sasha and Vova were born – twins were the first-born in the Badyr family. They spent two weeks in intensive care, they were discharged home with many diagnoses. Due to cerebral palsy and accompanying diseases, Sasha did not live up to 3 years. Parents threw all their strength into “stretching” Vova. And now in his map, there are only motor disturbances and speech delay. At the age of 7, the boy reads in syllables, but cannot speak clearly yet. Let's open the way for free communication for Vova!
After 15 years of waiting, Sasha’s mother finally saw 2 strips and realized that she would have a baby. Miracle! The boy was born prematurely in serious condition, doctors fought for his health. The fight began with an operation on the eyes, then there was resuscitation, later — a list of terrible diagnoses that still do not allow the boy to move freely and be healthy.
Maksym’s parents remember how happy they were during 2017 New Year celebration when the treatment ended. They had only one wish – health for the son! The boy lived in remission for two and a half years. He returned to his usual life playing football with his older brother, beginning to prepare for school... Suddenly the disease returned. A control MRI examination revealed a tumor.
- Giving tuesday 2019
- Kurazh bazar
- Change the world. give something yours
- Road to the heart
- New year
- Гастролі добрих речей
- Miles of grace
- Marathon 2015 - 2017
- Lviv half marathon 2017
- Interpipe dnipro half marathon 2018
- Kyiv half marathon 2019
- Kyiv half marathon 2018
- Kyiv half marathon 2017
- Kyiv half marathon 2016
- Kyiv marathon 2019
- Kyiv marathon 2018