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About us
We created Matteo Center so families of children with rare diseases can more easily find guidance, services that work together, and a community that understands.
From one family’s experience, for many more families.
Our story
In Matteo’s family, every assessment, therapy, and decision brought new questions. We learned how much energy it takes to move between specialists and how important it is for someone to see the whole situation, not only one part of it.
That is where the association began: with the wish to help other families find guidance, support for their child, and practical help sooner.
Assessment, intervention, and activities adapted to how each child learns, communicates, and develops.
Guidance and practical support for decisions about therapy, school, services, and family life.
Continued support for autonomy, life skills, relationships, and participation in the community.
How we choose to work
We listen before we suggest, build support around real needs, and keep the child’s dignity at the heart of every decision.
We see the person, their pace, joys, and needs—not only the name of a condition.
We bring family, specialists, and resources together so each step can support the next.
Children and their families deserve to be heard, informed, and involved in decisions that affect them.