Building Joy Together
This Christmas, let’s bring joy and strength to families living with MECP2 Duplication Syndrome.
With every donation, a new snowman joins our winter landscape, symbolizing another act of kindness and support for our community.
Your donation helps us support families directly, for example by helping them access essential medical equipment, therapeutic tools, and other resources that can make a real difference in their everyday lives.
Every gesture of generosity matters.
Every snowman adds a little more joy and support.
Together, let’s fill our winter landscape with snowmen and show families living with MECP2 Duplication Syndrome that they are not alone.
Together, we’re not just building snowmen. We’re building joy, support and strength for our families.
Thank you for your kindness and generosity this Christmas.
Your DupMECP2 team
Building Joy Together
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DupMECP2
Published: 11 Nov 2026
Beneficiary
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DupMECP2 Charity no. 1165516180 Email: office@dupmecp2.eu |
Our organization is dedicated to fighting MECP2 Duplication Syndrome and improving the lives of those affected by this rare disorder.
DupMECP2 was founded in 2022 by Caroline and David Covini following their son Matteo’s diagnosis. As scientists in the pharmaceutical industry and parents of an affected child, they recognized the urgent need to create a strong, united global community to expedite research for a cure and support families facing similar challenges.
At DupMECP2 we are building a network of doctors, scientists and families. We firmly believe that by bringing all MDS experts together, we can increase understanding of the disease, accelerate research for a drug and provide much-needed daily support for all.
In addition to this goal, our team's activities are very diverse: we raise awareness of MDS by organizing events, raise funds to support families and research, and ensure that the community stays informed about scientific advances.
