A year and a half ago Timofey underwent surgery to remove the part of his brain that sends out epi-signals to his nerve cells. At the time of the surgery, he was 6 years old, but in terms of development he was about the level of a three-year-old child. Exactly one year after surgery, the boy had not had a single seizure. In September, Timosha became a first-grader - a regular high school student!
But in October, Timosha had an attack - a mild and brief one - and it became a "bell" - a harbinger of possible recurrence of the disease. Then there were two more of the same kind. The parents rushed to the doctors and Timofey was urgently appointed an examination - a 24-hour video EEG monitoring. This will show what happens to the boy's brain cells and give an answer to what to do next.
The only thing the doctors are sure about is that the seizures will get worse if they will not be treated immediately. Help them to understand exactly what measures are necessary - a paid examination, help pay for the child to be examined! This year the family has not been quiet and calm - the son's health required travel for examinations, tests, medicines and serious expenses. Parents have no money reserve, and there is no way to collect them quickly.
