Creazione di centri di riferimento ospedalieri nelle regioni che ne sono sprovviste.
Assistenza materiale e morale ai soggetti portatori di Sindrome di Rett e alle loro famiglie.
Formazione di terapisti e professionisti.
Individuazione di terapie specifiche.
Promozione dell’interesse per la Sindrome di Rett e malattie similari.
Organizazione di Eventi
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