This name of this cutie is Polina. While most children dream of new toys for the holidays, Polina dreams of being able to walk, play with friends, just be. Polinka was born in 2011. And throughout her life, due to a rare genetic disease, she has a muscular weakness. She has one broken gene in the chain of her DNA. The gene that affects the work of the motor neurons of the spinal cord and they, in turn, are responsible for the work of the muscles, taking away the ability to sit, walk, roll over, cough, swallow and, eventually, breathe. Polina inherited this breakdown from mom and dad.
PROJECTS, EAST (10 of 86)
Delivery of health care for newborn infants can be compared, perhaps, to jewelry work. When a patient is about the size of your palm, you even breathe with fear, let alone give an injection or other painful medical procedure. Thanks to modern advances in medicine, doctors are able to save newborns, which are in critical condition, on time, even with a weight less than 1 kg. However, the goal of treatment is not only survival but also to exclude complications in little patients.
Dear friends! If you’re reading these lines, you aren’t just casual people in Artem’s life. So, you aren’t indifferent to mother’s Ponomarenko Halyna only son’s fate. She told us about her son Artem not so much. The boy’s already 18 years old. In short, he has a heavy form of cerebral palsy, microcephaly and epilepsy from birth. But this is quite enough for the child’s being sick from birth, as the doctors predicted. Nevertheless, Artem’s parents’ strong character and his persistent thirst for living have done a lot.
Angelok, so the mother gently calls Angelina. She has a twin sister Melania and an older sister Valeria. In November, the youngest girls Angelina and Melania turned 6 years old. Everything was nothing if Angelina was not sick. From the age of 2.5 years, this baby practically lived with her mother in the hospital. Analyzes, surveys, consultations... But the doctors did not succeed in putting the exact diagnosis. And only in June of last year, in the immunological center in Kiev, was it put to establish the cause of Angelina’s diseases. The girl has a congenital genetic disease: primary immunodeficiency, which deprives the body of natural protection.
Veronika is a skilled painter and she bakes extremely delicious cakes. The girl dreams of becoming a pastry chef and throwing a grand party after she gets well. But now the treatment goes on since Veronika’s leg is affected by a malignant tumor. After chemotherapy, the doctors prescribed surgery to remove a bone tumor and to insert an endoprosthesis. The prosthesis has come from the public procurement but the medical consumables are not available at the department. The girl’s mother is a single parent and she just cannot afford to buy everything necessary.
The war has split Donbass into two. Sadly, among those suffering from ongoing hostilities are children. To help nurse the wounds of their souls, they should be immersed in a peaceful life as soon as possible. In, 2017 the "Poshuk" (Search) tent camp has restarted its operation, and its plans for 2018 include active involvement of kids residing in the front-line areas, as well as IDPs.
"Hello, my dear helpers! This me again – enchanted Princess Nastia! Most recently, thanks to you, I returned from a magical country, where wonderful wizards and fairies helped me to remove the spell from my legs. Unfortunately, the spell was not completely removed, but in spite of this, we managed to remove several stages of the spells, and now I can stand on my legs and stand on all fours.
At birth, Sasha hung on a hairline between life and death: his mother's labor activity stopped during his birth. The doctors had to actually squeeze the boy out of the womb of a young mother. The boy was born, but did not breathe: he suffered a serious brain injury. So in the first minutes of life, Sasha got into intensive care.
Have you ever wondered what a teenager who was in adulthood feels, and there is not a close man or mentor left in the orphanage next to him? And if this teen is a person with a disability? Every year hundreds of boys and girls are graduated from the special boarding schools in Ukraine. Their further life depends largely on the luggage of knowledge and skills that they had obtained in state institutions.
With the birth of two children, the life in Ovcharenko’s family has been turned upside down. In the Kharkiv perinatal center, Dima and Vladik were born on a six-month term. In a fight for the life, unfortunately, Vladik died – he lived just 39 days. And Dima survived and with the diagnoses of child's cerebral paralysis and microcephaly, he entered a new stage of life for two.
- Kurazh bazar
- Change the world. give something yours
- Road to the heart
- New year
- Big love
- Kyiv half marathon 2019
- Гастролі добрих речей
- Miles of grace
- Lviv half marathon 2017
- Interpipe dnipro half marathon 2018
- Kyiv half marathon 2018
- Kyiv half marathon 2017
- Kyiv half marathon 2016
- Nova poshta kyiv half marathon 2019
- Kyiv marathon 2018