Timofei is long-awaited child. But epilepsy prevents him from normal development.
Timofei’s family is fighting for every achievement of their boy, but the peculiarity of the disease demands regular treatment in order to support the child’s development.
Islam grew up as an ordinary healthy boy. He did not suffer from any disease, was an active and a sunbeam child. He studied very well and was keen on Mathematics. But the life of the Gudkov family was divided into "before" and "after".
In February, the boy suddenly had a fever of 40 degrees. Prescribed treatment did not help, and the fever was not subdued. The boy started feeling pain in the leg. Doctors tried to investigate the cause of the illness, prescribing new drugs and diagnosing pyelonephritis, gastritis, Crohn’s disease, hip joint deformity, motor polyneuropathy...
But Islam’s condition worsened, and no one managed to find the reason. For 7 months the family has been trying to receive help in different hospitals, but with no result. Islam has epileptic seizures which last up to 20 minutes. The boy has not been speaking for several months already, and is only moving with the help of a wheelchair.
Thanks to your support we were able to raise the right amount of money to pay for the examination in ASSUTA Clinic in Israel.
Beautiful Emiliya was born 7 years ago. She grew up in a big loving family and brought joy to her family members. When she was just 2 years old, she already knew the main colors, could name them in Russian and English, knew animal species, could count to 10 and backwards, she used phrases in her speech.
8 years ago a girl with a beautiful name Kamilya was born in Tatarstan in the Khayrullins family. Kamilya “complete” or “perfect”.
However, the baby was born with congenital deformities of the spine. Thanks to the operation, which was done in Kazan immediately after birth, as well as numerous rehabilitation courses taken regularly until she turned 5 y.-o., the disease did not show up. As the girl grew up, leg pains started bothering her, while treatment was not bringing relief.
Unfortunately, the additional operation worsened the child’s condition.
Thanks to your support we were able to raise 49,742.00 USD to pay for an operation to eliminate spinal cord fixation, to release the nerve roots of cauda equina and correct vertebrae.
When two twin-sisters Khvostikovs were born and the world welcomed them, their parents were happy to the moon and back. However, only after some time doctors notified the parents that younger girl Sophia had a congenital malformation.
The girl is still baby, she is under 1 years old. Ksenia was born with a rare genetic disorder - Apert syndrome. It is a premature closure of the bones of the skull which usually happens by 3 years old. This early fusion prevents the skull from growing normally, its volume becomes limited which affects the shape of the head and face. In addition, intracranial pressure rises which leads to deafness, blindness and disability.