This association aims to support, accompany and help parents (family caregiver) of children from 0 to 20 years old with poly, pluri or sur-handicap. Family caregivers are often left to fend for themselves, with no status, no vacations, no sick leave and, above all, no adequate care facilities. When do caregivers take a break, take time for themselves, for their spouse, for their siblings, to go to the doctor for themselves? Where can they leave their children without having a knot in their stomach, where! That is the question. Very few temporary structures exist, they are there to make up for emergencies. Without forgetting the numerous administrative steps and especially the research too. Because the rarer it is, the longer and more tedious the research is and the places are very limited. Our goal and together for this inequality, to provide solutions, mutual aid and support. Our objectives are many: some short and medium term and others long term but they will all be implemented.