"And just want to say that I am happy with my life and don’t see any reason for discouragement. Although the situation is dangerous. Being 24 and reflecting on the beauty of the world, it is hard to give it up when there is still a chance to survive. I do not want to cause someone to compassion, much more wish your understanding. I will try as much as possible easy and affordable to explain".
PROJECTS (10 of 517)
Four months after the birth of Bogdan, they were hospitalized in a serious condition in "Okhmatdet", in the intensive care unit of chronic diseases. Diagnosis of a boy: a kidney disease of the 5th degree, bilateral hydronephrosis, congenital anomaly of the development of the urinary system. Later, the doctors delivered another neurologic diagnosis, which, as it turned out, was withdrawn. Almost four months, Bogdan spent in the hospital.
This is a very hard topic, but I decided to tell you, because now our family is in a difficult situation. For six years of treatment of child we have exhausted all our material resources and ask all not indifferent people to help our daughter to learn to walk and to see a real childhood without hospitals and pain. I will say that the birth was extremely difficult, the life of not only child, but also mine was under threat. Margarita was born for a period of 32 weeks with terrible hypoxia. As a resulthydrocephalus,
the defeat of the central nervous system, swelling of the brain, pneumonia, cerebral palsy.
In 2015 and 2016 thousand philanthropists helped save the leg of a seven-year-old Igor Statkevych from amputation. Heavy pathology vessels struck his right foot, causing the destruction of his entire body. Ukrainian doctors had predicted an amputation, but a number of preliminary operations in Germany were allowed to keep the child's leg and slow the progression of the disease. Your donations have helped the boy to go and study- he went to the second class in the autumn. Now Igor needs urgent knee surgery to replace a titanium plate in the leg . Operation is scheduled for the summer in the clinic of Holle. It cost 17 470 EUR.
A beautiful girl runs on the beach. Her brown hair is developing the wind. She runs towards the little smiling girl with a cry of joy: "Mam!"... And here Nadia is waking up. This dream Boyars Nadia from August 2016. That's when she was diagnosed with acute T-cell leukemia. Since then her dream – a family, children, quiet life only exists in dreams. Since the disease has already passed the entire complex course of chemotherapy, each stage was given very difficultly, with severe consequences, mainly with a significant excess of blasts and liver hepatitis.
We raised funds for Daniela, who were transferred to the clinic of Israel. The girl underwent a course of treatment, but since the clinic account left UAH 12,583, and Daniela no longer needs active laboratory research, the remaining funds will be spent on physical examinations of Topalova Lyudmila and Nadezhda. They suffer from chronic diseases. For more information, see the documentation.
Orphan. A terrible word for parents. Orphan means rare. Orphan diseases are diseases that dump 5 people per 10,000 population. Orphan diseases are diseases that either have expensive treatment or do not have any treatment at all... There is Yaschenko Danylo, he is orphan. Danylo has Duchenne muscular dystrophy, is a genetic, exclusively male disease. In Ukraine, the life expectancy of Dania is 20 years...
Collection of money is stopped. Actual information is accommodated in the blog of the project.
8-year-old Valeria does acutely need for help. Her heart is constantly enlarged. All her life the little girl lives on medical prescriptions: she is not allowed to run, to dance, she even drinks water only at scheduled times and in limited quantities. In addition, she is forced to take regularly medication up to fifteen pills a day, several times a year to pass the consultative examinations at clinics. But now her life is hanging by a single thread.
The boy is in the queue of the Ministry of Health to pay for foreign treatment. But the money for this program was allocated only on paper. Waiting for all bureaucratic procedures David had virtually no chance. Therefore, they decided to collect at least part of the funds to fly to Turkey and start treatment as soon as possible. The money that was transferred for a small David is enough for Turkish doctors to take the boy now and he got a chance to live and waited for the Ministry of Health to transfer the remaining amount for treatment.
"We have an ordinary family, a second child is our princes. As we wanted: the boy and the girl. Diet, doctor’s prescriptions, tests. Fast childbirth in time, breastfeeding. It was a lovely child; there were no problems with her during first six months. And then everything turned upside down... I look at Kira’s photos, there are walks, and ponytails, and brother, and christenings, and toys, and smiles... Then the onset of the disease – the first lymph node, then the bandages on the rest lanced lymph nodes, the first hospitalization, catheters, bruises because of low platelets, anesthesia, drips, chemotherapy, pain, resuscitation...