The child suffers from a severe form of epilepsy that per day on 110 carries seizures. Now his family is raising money for treatment in the United States until the boy has not lost his ability to speak.
Lennox-Gastaut Syndrome
13-year-old Scottish Max McGee suffering from severe shape
childhood epilepsy -
Lennox-Gastaut syndrome . This is not only difficult, but also a very rare kind of disease resistant to all drugs. Every day the boy shaking dozens
seizures And sometimes their the number of passes and 110 per day. Max's condition worsened due this is so that he may soon lose the ability to speak.
Lennox-Gastaut Syndrome
His family collects 65,000 pounds for a trip to Miami, where the child was offered alternative treatment. He's at home in Scotland doctors nothing can be done. In the first week of your stay in the heart of the US Max will go through a variety of techniques to determine which of them gives result. Well, the next visit, which will last two weeks, the boy will receive the same treatment selected.
Lennox-Gastaut Syndrome
Currently, the child takes 5 different drugs, that almost no help in deterring
seizures . He recently I passed through the implantation of a vagus nerve, and the doctors found him a small box in the armpit area, which should help in tracking and monitoring seizures. But as soon as the implant is activated, Max suffered a seizure, which lasted 30 minutes. His parents were terrified because they thought lost his son.
90% of the time a child spends in a wheelchair, but he still loves to play football with friends who actively help to collect funds for the treatment of Max. (READ MORE)
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Healthy Child
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