Five-year-old woman who lives in Toronto has earned 25 thousand dollars on the implementation of lemonade. Therefore a small canadian wanted to collect cash for the treatment of his brother suffering from a rare genetic anomaly.
Inhabitant of Canada na'ama Uzan opened their views on the implementation of lemonade and buns to raise money for treatment of his brother, tells Lifenews. The brother of the girl suffers from a rare form of a genetic disease is Angelman syndrome.
Seven-year-Nadav found a mutation of the 15th chromosome. He actually walks and talks, as well as continuously suffering from cramps. While doctors have not found a method to cure this disease. The only thing you can do is significantly improve the quality of life in patients with Angelman.
Despite this, the five-year na'ama Uzan doing everything possible to help his own brother and all remaining people with this terrible diagnosis. Selling lemonade and cookies, for the year the girl earned 25 thousand dollars. She collected funds transferred to Fund the treatment of Angelman syndrome (FAST).
Once the story got so Busy in the local media, many people were inspired by her example. Thus, the occupant of California David Lowe together with his wife gathered 20 thousand dollars to help his own son, to a patient with Angelman syndrome. The funds collected the pair in addition have listed in FAST.
Angelman syndrome is a genetic disease in which the patient has mental retardation, sleep disturbance, seizures, chaotic movements of the hands, and frequent laughter and constant smile on his face. The result listed hallmarks of the disease is often called the "syndrome smiling puppets".
sections: Society, World News |