Who are we
The goal is to give every child who, like me, has one or two small ears, the chance to access the necessary care!
To reconstruct my little ear before I start CP, we have to do it in the United States, the cost is very high, it is to participate in the financing that the association was born!
To hear the noise like everyone else!
Our Mission
Our mission is multiple: even if it is primarily oriented towards Soline, the needs are immense:
Allow Soline to have 2 ears to hear like all children:
To offer Soline the same opportunities for brain and language development, as well as the self-confidence and professional rights that any child can dream of aspiring to.
Raising funds to finance aplasia-related operations and costs:
Fund surgical operations and costs related to the operation of a child with aplasia (microtia and atresia).
Raising awareness of aplasia:
Inform about the absence or deformation of the ears and the absence of the ear canal, the consequences, compensatory and alternative technologies.
Provide moral, material and financial support to families.
Create a chain of solidarity:
Help the child and his family to face the material and financial consequences for their daily life and development.
Contribute to the child's well-being and compensate for or repair their disability.
Informing families and the general public:
Informing families with children with aplasia.
Mobilizing the general public on aplasia.
Raise awareness among healthcare personnel about hearing aid techniques and technologies.
Support and advise families:
Help with the procedures for operations, equipment or the creation of an aid association.
Networking families and health professionals to help with support and identification of factors of aplasia.
Seeking funds for various needs:
Pay for therapists, accommodation and transport costs, as well as therapies and comfort materials not covered by the appropriate organizations.
Offer training:
Provide training related to the objectives and operation of the association.