The list of needy

It is difficult to imagine what a fragile little girl went through. How many courses of chemical and radiation therapy she had to go through. Relapse after relapse, the spread of metastasis throughout the body, bone marrow transplantation is an endless series of tests.

Two years ago, the boy was diagnosed with rheumatism. "It’s genetic" - concluded the doctors. Therefore, at first, no one paid any attention to the pains in the legs that intensified last spring. But the temperature kept at around 37.5 was alerted. Their walking on the diagnostic departments began. But nobody could answer to the question "what about the child".

Khadizhat Ismailova is 64 years old. Last year, due to doudtful symptoms, an incorrect diagnosis was made: pre-heart attack state.

A large family’s from Saratov region. There are five children in the family. The youngest son was diagnosed with: Neuroblastoma of the retroperitoneal space of a malignant character, stage 3. The child’s been treating for almost eight months in Moscow in Blokhin pediatric hemology and oncology. He underwent four courses of chemotherapy.

A child received her bad diagnosis in one month old: spinal muscular atrophy Verdniga-Hoffman type 1. This is a rare genetic disease as a result of which the atrophy of all muscles develops. The outcome of the disease is sad.

Aisha Dzaurova is six years old. Diagnosis: cerebral palsy, mental retardation. Together with her sister, they split everything in two equally: toys and sweets, their parents’ love, and also walk together. It is hard to believe that four and a half years ago, Aisha fought hard for her life and won.

Ashahanova Napisat is 7 years old. Diagnosis: Cerebral Palsy. The girl did not know how to crawl and particularly walk. Parents took their daughter for counseling, treatment and rehabilitation. All that helped: at 10 months, Napisat began to roll over, to crawl, at 1 year and 2 months she got on her hands and knees, crawled in 18 months old.

Patimat took her son to CT scan. After that, they came to a consultation with an oncologist, where a severe diagnosis of “lung cancer” was made and a buildup of fluid was found in the lungs.

The girl was born prematurely. She had hydrocephalus, and cerebral palsy was made as a concomitant diagnosis. The baby girl had a shunting operation on her head. But Fatima, unfortunately, cannot sit or crawl on her own....

Today, doctors encourage Elvira with good results. But for carrying out further treatment and maintaining the immunity of the young girl at a level sufficient for life, huge funds are needed. And without our help, these chances can collapse.