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What do we do?

« Genetics make us unique, yet ordinary individuals. It rarely makes us as extraordinary as all children with MECP2 duplication are. »

David Covini, President

« Genetics make us unique, yet ordinary individuals. It rarely makes us as extraordinary as all children with MECP2 duplication are. »

David Covini, president

Our mission

Support to families

Share experiences with families awaiting diagnosis and improve the lives of children.

  • Newly diagnosed
  • Medical and therapeutic care
  • Exchanges between families
  • Testimonies of relatives
  • Useful documents and links
 
 
 
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Inform about research

Monitor the progress of research projects and inform families of scientific advances.

  • Current projects
    • Antisense oligonucleotides
    • Repositioning
    • Interfering oligonucleotides
    • CRISPR
  • Registries
  • Expert webinars
  • Publications
 
 
 
 
 
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Raising awareness and funding projects

Identify projects and participate in their funding through fundraising and donations while raising awareness of the syndrome among the general public and physicians.

  • Raising awareness
  • Funding projects
    • Fundraising
    • Donations
  • Our fundraising
  • Our donors
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We are here for you

Do not hesitate to contact us and join our fight

Become a member
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