Acma Onlus

We provide financial support to families with children born with severe rare malformations that require reconstruction and lengthening. The alliance of families and volunteers who raise funds through sales of Christmas products, donations, 5 x1000. Born in 2018 at the behest of Nicole Barile’s family, she was born with a severe malformation in her right limb, but supports many children who turn to the association. What shall we do? We support the expenses not covered by the National Health Service, which are still borne by families; we promote free awareness projects aimed at promoting the inclusion of diversity in schools and events on the territory, We help the families to find the right path through bureaucracy and psychology.