Toujours un Sourire

Purpose of the association

To combat delays in the management of neurological sequelae following heart surgery for congenital heart disease by improving the information provided to parents, about the various long-term effects children may experience and the different treatments available in France and abroad. To raise funds to enable Meylie and other children with neurological sequelae resulting from congenital heart disease following open-heart surgery, to access treatment not covered by the National Health Service and improve their daily lives through personal or practical support (pushchairs, car seats, adapted beds, etc.) Fund intensive rehabilitation programmes abroad, subject to availability; Foster connections between parents of children with disabilities, through meetings and events. To support families of children with disabilities. To bring about social change for the better integration of people with disabilities. To raise awareness of other existing organisations in order to provide the best possible support for families

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