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This Saturday evening in February, Laure Salomon is moved. The president of the association Un espoir pour Tya, her 9-year-old granddaughter suffering from a rare malformation of the cerebellum, has in front of her a full house of 360 people, who have come for her lotto in Étampes (Essonne). Shopping vouchers are up for grabs. But most participants are here to support the cause.