"Please do not put a period, this is not the end! Life must go on!", Artem's parents asked doctors. But onco-hematologists of OKHMATDYT have eliminated his son from the list of children with perspectives. They have failed to overcome the congenital lymphoblastic leukemia in the 1.5-year-old Artem Makhno with standard protocols of chemotherapy. After quick relapse doctors have sent the child home, offering parents to prepare for the worst. But there are methods to help Artemka already well-known in the world.
HEALTH (10 of 532)
191 111 753.81 UAH collected in category Health
249 441.67 UAH - скарбничка категорії Health
UPD: The Ministry of Health of Ukraine allocated funds for the treatment of Yasmina in Italy, so we stopped the collecting money on the UBB website. Detailed information in the blog of the project and in the heading "Documentation". Thanks to everyone who supported the girl!
Little Yasmina is not even two years old but she has already spent one-third of her life in hospitals. She had to be examined plenty of times, these were punctures and biopsies, Yasmina stayed with five various medical institutions and had been operated several times followed by chemotherapy. Now she needs one more chemotherapy course and bone marrow transplantation abroad which costs EUR 125,000. Since August 2018 the parents fight for their daughter’s life as hard as they can.
"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".
Lyonchik and Lyonushka – so affectionately call his parents. He is 5 years old, but so far he speaks only individual words. He is five, but in his family, he is 4 years old. Prior to that, he lived in the Krivyi Rih Children's House. In June 2014, he met Yulia and Vadim, and in July he became their son. And in the autumn after the examination, the audiologist, without particularly choosing the expression, told mom and dad: “Your child does not hear. He will lag behind in development and the boarding school shines for him".
Vika is an orphan, disabled of the 1st group since childhood. Now her state of health has deteriorated significantly, compared to previous years. A woman has diabetes mellitus type 1, severe form. At the age of 20, she completely lost her sight, she had her left foot amputated. Because of injuries, the destruction of the talus of the right leg began, which is constantly progressing, as a result of which a limb was shortened. Vick has become difficult to move around. But despite the dire state of health and the death of relatives, Vika does not give up.
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.
UPD: The Ministry of Health of Ukraine has allocated funds to pay for the operation for Nadia in Turkey. Detailed information and relevant documents can be found under the heading "Blog" and "Documentation".
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.
Preschoolers Nastusya and Timofiyko, schoolchildren Sasha and Vitaliy, students Denis and Yana – what unites them? All of them were born with a genetic disease, cystic fibrosis. This is a rare disease, which is strikes, first and foremost, in the lungs. Abnormal thick mucus blocks the lungs, causing severe infections that provoke obsessive coughing, pneumonia, bronchitis and other complications.
UPD: according to the Operator's assistance, the Ministry of Health of Ukraine allocated part of the funds for Sasha’s treatment at the same time collected funds for the UBB will also be transferred to the clinic for treatment. Detailed information in the blog of the project and the heading "Documentation". Thanks to everyone who supported Sasha!
"Look for the money! Sasha urgently needs a bone marrow transplantation!", such terrible words Sasha's parents heard in the hospital. No one even could have thought that a few months prior to Sashenka Emets’s first birthday his parents would learn about the dreadful diagnosis of their son: juvenile myelomonocytic leukemia. Sasha is very small, but he is a very big fan of dogs. He just adores them, his beloved dog is still a toy, and his name is Buff.
"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...
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