This blog is intended for families, researchers, and professionals interested in better lives for children and adults with MECP2 Duplication Syndrome.
Pam Albert's MECP2 Duplication Syndrome Website provides a great deal of useful information for families and profiles of many of the current children and adults diagnosed with this condition.
Facebook users who are members of families if individuals with MECP2 Duplication syndrome may wish to join the Facebook MECP2 Duplication Syndrome Family Talk Group for discussions of family matters.
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Visit the 401 Project or Donate.. Click image below.
MECP2 Duplication Syndrome Fund
Click here for information on Donations to the Rett Syndrome Research Trust's MECP2 Duplication Syndrome Fund