When I came to your door, my child was 6 months old and we were using 3 strong antiepileptic drugs: TEGRETOL, LUMINILATTEN, and TOPAMAX. As if these weren't enough, you also inflicted the curse of EPDANTOIN upon us, and thanks to you, we learned about its most prominent side effects through struggle and experience. For two months, my child has been teething day and night, screaming and crying because of the thickening and swelling of the gums, which is known as the most prominent side effect of this cursed drug. And this drug, with its side effects, has an exit from our lives, and we still haven't been able to get rid of it, even with the doctor's guidance and by gradually reducing its dosage. Seizures that don't stop after 2 or more doses are referred to as drug-resistant epilepsy in the literature, and if the child is ready and compliant with this treatment, the only known treatment is the KETOGENIC DIET. Instead of inflicting this curse of EPDANTOIN upon us, why didn't you recommend the KETOGENIC DIET and save us from this drug? You exhausted us for months with the side effects. When I said my child couldn't tolerate this medication, became drug-induced, cried like a cat for hours, had excessively high body temperatures, and couldn't sleep, why didn't you CHANGE THE COURSE OF TREATMENT? And you know that sleeplessness and stress are the biggest enemies of seizures. Those medications are poisons; they shut down my child's perceptions, disconnect him from life, make everything about him artificial, and they DON'T STOP THE SEIZURES. They are just poisons that profit pharmaceutical companies; otherwise, they have absolutely no benefit for resistant epilepsy. You stole months of our time, you stalled us. You only stall in genetic diseases. I tell everyone, if your child has resistant epilepsy along with a genetic mutation, and the tests done during the preparatory phase show that they are compatible with a KETOGENIC DIET, never waste time with artificial medications that disconnect your child from life. (And then, on an examination day, you told me you saw my child looking very good and that you were waiting for my Google reviews. My child has no neck control, no eye tracking, is a floppy baby, and continues to have seizures. How could you have seen my child looking good that day? How could I have given you positive reviews when I had unanswered questions and my child wasn't making any progress? Well, I'm giving you my reviews now, based on my own experiences.)