How we born
When I discovered that the child I was expecting was suffering from this syndrome, I looked for information everywhere but I could not find any because there was no association regarding and the medical literature only described the most serious cases and instead I discovered life beyond the disease.
Thanks to social networks I discovered other parents and affected people around the world who described the disease as something different and so after just two years after our son was born, we founded this association with the aim of becoming an international reference point.
And we succeeded.
President & Founder of CESI onlus
Help CES Children
Being a reference point – to hearken and debate – for all people affected with CES or similar malformations.
Fundraising in order to spread a worldwide awareness of the syndrome.
With the aim of identify causes and specific treatments for the most recurrent characters.
How You Can Help Us
Call us at +39 392 92 17 140 to make a donation and become a special donor.
Founder & President
Founder & Vice President
Council Member & Psichoterapist
Become A Volunteer
You can help us online or offline. Write us for more information.