They waited for a small miracle over two years. And the miracle happened – a gorgeous girl was born. But unfortunately parents’ joy was very short. For parents to hold on to these small little hands an urgent bone marrow transplantation abroad needs to be done. But they have no money for the operation, treatment and rehabilitation.
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Children with this diagnosis do not live - the mother was told in the hospital. And my daughter will live! - the mother of little Diana claimed to the entire world. Here you have the opportunity to help fulfill the promise of a courageous woman, and prove that love, compassion, faith make wonders! The only chance for the baby to survive is the bone marrow transplantation abroad, the money to pay for which the family would nether gather themself!
The Ministry of Health of Ukraine has allocated money for the operation for Vadim.
Kidney failure. Most of us have met this expression, perhaps, only in the list of contraindications to medications, looking quickly through the sheet and feeling relieved, that it not about us. Vadim Vorchilo has been living with that disease for 15 years. The life of the boy was happy, but one day his condition deteriorated dramatically: Vadim began to choke in the night, there were nausea and bad appetite. After the examination, doctors diagnosed – terminal chronic renal failure (CRF).
A 9-year-old girl really wants to live but in Ukraine she cannot get help – for almost two years all available treatments have been exhausted. There is only one hope – treatment in Germany! To overcome neuroblastoma – a large tumor in the retroperitoneal cavity – our little princess needs help of the others. She needs help of those people who don’t know her but they still do care about her.
Sasha was born 7 years ago. He was long-awaited baby. But because of doctors’ incompetence (the child was vaccinated on the first day of life). Sasha was diagnosed with infantile cerebral paralysis. It was a terrible blow for the family. But we are not giving up. We decided to fight.
Participate in the X factor dentist Sergei Gladyr persuaded his little son Danya. Kid likes how his dad sings so much. Charming boy with huge brown eyes and a gentle gaze, like his sister - twins, will soon be 7 years. In his 7 this little man has gone this courageous man who persevered in the struggle with his terrible disease. Don’t remain indifferent. Danya needs your help to make their first independent steps.
Roma is only 2 years old but he has passed a long way fighting his terrible disease. After a few weeks his treatment at the hospital in Kyiv comes to an end but to overcome the disease it is necessary to undergo additional therapy at the medical center abroad. In a few weeks the Italian hospital is waiting for Roman and his mother to start treatment. There is no time to wait at all. We beg you to help this little one in his fight for life! Please, help Rom’s family to raise money for treatment!
The story is about 3-year-old Misha. However, we will start it with a story of Olya Silantieva. Do you remember the girl from Dniprodzerzhynsk with exstrophy of bladder? After four unsuccessful operations in Ukraine, the girl had an operation in Serbia, where doctors managed to close the abdominal wall. Mykhailo Podgorny was born with the same anomaly. He has even overtaken Olga – suffered five transactions for 3.5 years. Like Olya, Misha had persistent fistula – a dangerous thing, an open gate for infection. And the boy is promised 100% guarantee for successful solution of the problem in Serbia.
Roma is the first child of young Alexander and Tatiana. They wanted and expected him so much. Mother conscientiously underwent all necessary medical tests, US examinations, kept to a diet. All conducted tests showed that the pregnancy was proceeding the way it should and the newborn child would be healthy. And then it was time to go to thematernity hospital and here the life of young parents became a nightmare.
3-year-old Misha has been under treatment in an oncology clinic in Israel for almost a year. He has undergone 8 blocks of chemotherapy, a tumor surgery and adrenalectomy, bone marrow autotransplantation and radiation therapy. Doctors call him “our unique child” because his body always reacts positively to each step of the treatment. As you know free medical care does not exist nowadays, and this is exactly the case when you need to buy A CHILD'S LIFE!!! However, the cost of treatment is something the 3-year-old Misha’s family cannot afford. It’s truly frightful to think that there is an opportunity to help, but it cannot be done on one’s own...