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Hello everybody. My name is Evgeniy, Odessa (Ukraine) I am the father of a charming one-year-old girl Aliska. A year ago, two events knocked on our family at once:
1- I was lucky to become a dad.
2 - the most unexpected and terrible thing is the disability of a little baby. From the doctors at that stage, except: "God willing, slip through" I did not hear any more intelligible. A year has passed and nothing has changed. My daughter suffered greatly even in utero: 1. CHAZN (partial atrophy of the optic nerves) of both eyes, how much? Until now, we have not found an answer; 2. Corpus callosum hypoplasia, secondary microcephaly; 3. Moderate hyperopia; 4. Flaccid tetrapes; 5. Secondary moderate hyperhomocysteinemia; 6. Secondary mitochondrinal dysfunction; 7. Symptomatic focal epilepsy. There are many diagnoses, few solutions, one thing we know for sure she needs high-quality rehabilitation. We have already undergone more than 8 courses of massage, 5 acupuncture, 2 courses of Vojta therapy, Bobat therapy, as well as drug treatment in the amount of about $ 6 thousand for immunoglobulins, and elimination of toxins from the body, as well as a cure for the TTV virus. And unfortunately, our financial situation has already gone into the negative for a long time, we do not lose hope and faith in our girl, as well as in your kind and caring hearts. Her psychological state has improved, she confidently leans on her forearms, recognizes her loved ones by their voice (thank God she has excellent hearing); understands that now there will be a procedure and it will be painful ((plays with toys by touch, unfortunately.
Our neurologist said for sure that until the age of 3 if we do not get on our feet, then only cerebral palsy is worse, and also until the age of 7 we have a chance to compensate for epilepsy and there we are also at risk, made it clear that the chance is very small, looking at our defeat, but it is there and our family is not going to miss it.
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