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Storie di ragazzi che non hanno tempo

Giorgio-16 anni, malato di Lafora

WHEN I GROW UP I WILL BE…

Posted on 29 April 202422 July 2024 by Tiziana D'Izzia
My name is Romina, and I am Giorgio’s mother. Giorgio is a 15-and-a-half-year-old boy. At the age of 11 and a half, he had his first tonic-clonic seizure, something he had never experienced befo[...]
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THE STRENGTH OF MOM PAOLA

Posted on 5 April 202223 July 2024 by Tiziana D'Izzia
We are learning about Lafora Disease through the stories of girls like Martina and Carola who live with it every day. Unfortunately, there are also girls who have faced this disease, fought against it[...]
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The Story of Carola

Posted on 4 October 201922 July 2024 by Tiziana D'Izzia
There are only 200 people in the world like Carola, 16, from Fiumicino, and 30 in Italy. Two hundred children and adolescents are condemned because there is still no cure for Lafora disease, a genetic[...]
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TEMPO ZERO ODV

Help us stop lafora disease

TEMPO ZERO ODV - Non-profit association created to help research on Lafora Disease and to help families affected by this disease who no longer have time

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