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Hello is Serena, I have 2 years are suffering from epileptic Encephalopathy, was born to fight against my pluriquotidiane crisis reach the United States to treat with the Synergie Hbot, but to do this I need your help ...
Serena's parents have not let stubborn, are trying in every way to overcome these moments that last for a long time already, I am obstinate and rightly so. And you wonder if in your power to be able to support the cause, and to make visible as possible within this announcement, maybe turn the link: www.unsorrisoperserena.com to friends and people that year to help the faculty famiglia.Visitate the official site and in person you will see how an entire region and mobilized, we try to raise funds in order to transfer profits in the U.S. the period of care requiring SERENA. There are instruments of the law, there are opportunities for funding and access to coverage contributions TOTAL expenditure, but as in all things in Italy even in cases such as politics, leadership, those directly involved in the work, always releasing the ball others (indifference) and becomes a more of a black tunnel. Forty family Mom and Dad for years Serena tried everything in every direction, for exercising their favor in the law but still the world bureaucrat and not activated, and meanwhile the little that Serena dovrbbe already be game for more than 3 months and still in Italy, and suffering.
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