Resources and stories
We write about questions after diagnosis, family support, inclusion, and life in the Matteo community.
· 3 min
On September 17, 2026, Matteo Center Association officially opens its physical facility in Bragadiru: a warm, safe space tailored to children with rare diseases and their families.
· 21 min
A comprehensive, evidence-based guide to Williams syndrome in children: genetic foundations, clinical features, cognitive profile, recommended evaluations, and early intervention.
· 2 min
We share the beginnings of the association, the people who joined us, and how a community grows when it chooses to stay close.
· 2 min
Family support is not limited to isolated information. It is about time, clarity, empathy, and access to people who understand the weight of everyday life.
· 2 min
A rare diagnosis brings many questions. We write about Williams syndrome, why clear information helps, and why early support can make a difference.
· 3 min
From May 30 to June 1, Matteo Center Association brings families, children, specialists, and partners together in Bragadiru for integrated rare-disease support.