Katusha is a very cheerful and sociable girl. But on the first day of her life she had an epileptic seizure, which started her fight for health.
Up to a year Katya's life was endless hospitals, examinations, tests and clarifications of the diagnosis. They diagnosed her with epilepsy due to a brain defect, focal-cortical dysplasia, and prescribed anti-epileptic drugs. Before the age of 4, Katya had a lot of breakdowns in remission of the disease, so the medications were often changed. After a while her seizures became too numerous, up to 60 times a day. The family applied for consultations to the Tyumen neurosurgical center, where the girl was invited for surgery.
After the surgery, Katya began her recovery period: she began to learn to walk and eat again. Now the girl is being observed by an epileptologist, an orthopedist, an endocrinologist. According to doctor's prescription Katya needs a genetic analysis - complete sequencing of exome - to clarify a number of drugs, which are harmful to the body and do not help to improve the condition of epilepsy.
We ask for your help in paying for the analysis for Katya so that she can forget about her seizures and be a full-fledged child who loves this life so much!
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